Home > Training Search > D > Document > Web-based Seminars

Document Web-based Seminars

Document Training Provider? - Tell us about your Training!
on-line e-learning cbt (computer based)
online course
 instructor led training
instructor-led class
 study at home
learn at home
 group study and discussion
group study
 self directed
self-directed study
 cd rom
cd-based training
 DVD
DVD video training
 book
printed book
 e-book
e-book digital book
 workshop / seminar
workshop seminar
 train the trainer
train the trainer
 computer lab
computer-based learning
 special pricing!
discount pricing
 on-line tutorial)
online tutorial
Document Training Seminars and Classes
From Requirements Solutions Group
How to Find and Build Test Cases from Business Requirements instructor led trainingon-line e-learning cbt (computer based)group study and discussioncoursewareexercises, case study ...ngineering techniques to identify scenarios to be tested, document the setup criteria, script the execution steps, and establish how to quickly evaluate whether the solution passed or failed the test. You will learn how to use business requirements, stakeholder requirements, solution requirements, transition requirements, use cases, and scenarios to identify and define test cases. Note: This  more...
How to Define and Document Use Cases instructor led trainingon-line e-learning cbt (computer based)group study and discussioncoursewareexercises, case study ... structure of use case diagrams and the business use case document, use cases can quickly become "useless cases". This training workshop offers use case training in the basics of use case documentation and business use case diagrams as tools for business systems analysts. It explains the who, what, when, where, why and how of business use cases and use case diagrams. Note: This  more...
How to Analyze and Improve Business Data instructor led trainingon-line e-learning cbt (computer based)group study and discussioncoursewarecase study, exercises Using business data model to identify potential business problems that are caused by missing or improperly defined business data is the next step in the progression from dataa asa aa problem to dataa asa aa valuablea resource. This on-line business analyst training workshop assumes you know how to draw business data models (entity/ relationship diagrams). It is designed to give you a  more...
How to Build Business Data Models instructor led trainingon-line e-learning cbt (computer based)group study and discussioncoursewarecase study, exercises Business data represents the atomic level of information systems. It forms the basis upon which everything else depends. In a very real sense if you get the business data right, the rest will follow. If you get the business data wrong, the system may never recover. In order to get the majority of the business data right, it is essential to have a picture of the data in form of a business data  more...
How to Elicit Business System Requirements instructor led trainingon-line e-learning cbt (computer based)group study and discussioncoursewareexercises, case study It is very early in your project. How will you, the business system analyst, and the business subject matter experts (SMEs) determine what the system should do when you are finished? There are many people involved, each with different expectations and needs. How can you deal with these difficulties, gather reasonable requirements quickly, and not waste the effort? This training workshop offers  more...
How to Write Effective Business Requirements instructor led trainingon-line e-learning cbt (computer based)group study and discussioncoursewareexercises, case study Writing effective business requirements is a critical skill for subject matter experts who represent the business interests on an IT project and for business analysts. The challenge lies in defining business needs in the form of business requirements, stakeholder requirements, solution requirements, and transition requirements that other audiences will interpret as intended and use to design the  more...
How to Analyze Sets of Business Requirements instructor led trainingon-line e-learning cbt (computer based)group study and discussioncoursewareexercises, case study Understanding the business requirements in the manner in which they were intended can be a very challenging proposition. If the requirements are going to do their job well, they need to be understood by several target audiences, namely the business community, the technical community, and the developer/ tester community. Each of these groups needs to be able to read the business requirements and  more...
How to Package and Communicate Business Requirements instructor led trainingon-line e-learning cbt (computer based)group study and discussioncoursewarecase study, exercises One of the primary jobs of the business analyst is bridging the communication gap between the business community and the technology experts. Business, stakeholder, solution, and transition requirements describe what information technology has to deliver but making sure that both parties agree on just what these requirements mean is the real challenge. This virtual workshop presents concepts,  more...
From Kogent
BOW320 - BusinessObjects Web Intelligence XI 30 - Advanced Report Design - Virtual Class ...resent and analyze this information in a Web Intelligence document. This one-day instructor-led classroom course is designed to give you the comprehensive skills needed to apply alternative query and reporting techniques when creating complex Web Intelligence documents. After completing this course, you will be able to create combined queries and use sub-queries. You will also be able to use  more...
From THOMAS HOUSTON associates, inc
EMPLOYEE DOCUMENTATION AND RECORDS RETENTION Various OFCCP regulations require that contractors preserve complete and accurate personnel records and to permit the OFCCP access to their records, including computerized records, for inspection and copying. Upon completion of this program the trainee will have an understanding of: The different OFCCP regulation retention period requirments When / how it is permissible to transfer  more...
From Single Sourcing Solutions, Inc
Configuring the Arbortext Application Tutoring instructor led trainingon-line e-learning cbt (computer based)study at homee-bookworkshop / seminardesktop sharing, individual tutoring ...hitect that enable you to create, configure, and maintain document types. You learn about user interface configuration, the DCF file, and document type preferences as you master new terminology and skills. After completing this course, you will know how to open Arbortext Architect, and import doctype components; you will also have a solid foundation in the fundamental skills required to  more...
Authoring with Arbortext Editor (Tutoring) instructor led trainingon-line e-learning cbt (computer based)study at homee-bookworkshop / seminardesktop sharing, individual tutoring ...u will know how to open, save, and close new and existing documents in Arbortext Editor. You will learn how to perform basic edit operations, such as cut, copy, and paste. You will also learn how to find and replace text and markup. You will learn how to insert, change, and delete markup and text. You will learn how to insert graphics and symbols, create and insert text entities, and add,  more...
Authoring with Arbortext Editor - DITA Edition (Tutoring) instructor led trainingon-line e-learning cbt (computer based)study at homee-bookworkshop / seminardesktop sharing, individual tutoring ...You will learn basic functions such as opening and saving documents, replacing text and markup, adding and modifying attribute values and creating topics, tasks and references. You will also learn how to use the Resource Manager to create cross-references and links, create content references, and insert graphics and images. You will also use profiles, compare document versions, create DITA  more...
From Future Media Concepts
Adobe Acrobat Complete - Online ... cross-platform capabilities allow you to distribute your documents efficiently without sacrificing the original design. When you need to distribute your documents to viewers using a variety of platforms and software - Acrobat is your tool of choice. This three-day course provides an excellent overview of how to convert your work into Adobe Portable Document Format (PDF). You will learn how to  more...
From Last Minute Training
Word 2007 Document Formatting I teleseminar Do you want to make your documents look more professional? Do you want to enhance the text within a document with font changes, borders, or shading? Do you want to create numbered or bulleted lists, or change the way text lines up on the page?  more...
From Internet English Learn Online
Document Editing ...documents written in English, from CVs and cover letters, to important business memos, those vital academic papers or even your websites and e-mails. For just a small fee you can ensure your documents have perfect English. Relax, and let your IELO teacher give you the peace of mind that your document is flawless. So choose IELO, because sometimes you can't afford to make any mistakes!  more...
Internet English Learn Online Custom Course If for any reason none of the English courses offered on this website suit exactly what you want, then please don't hesitate to contact us. IELO is committed to ensuring only the highest quality of teaching in our English lessons and we are dedicated to satisfying every student's individual needs. Our experienced course developers will be more than happy to work with you to give you the English  more...
Exam Preparation IELO focus mainly on the three most popular English language exams: FCE CAE IELTS This list is by no means exhaustive. If there is any other type of English exam you are studying for, an internationally recognised qualification in English or an end-of-year school exam, IELO can help you achieve your goals! Students who wish to study these, or any other English exams, must be focused  more...
English for Special Purposes IELO Courses - English for Special Purposes If you are looking for a more focused English course, for work or for study, then IELO offers the following specialist subjects: Academic English Business English Nursing English English for Telecommunications and many more . . . If you need English lessons for any other specialised area, IELO would be happy to develop a course with  more...
English for Jobseekers Are you struggling to get a job in an English-speaking country, or for an English-speaking company? Do you think your level of English is holding you back from advancing in your career? Would you like to gain an advantage over those in a similar position to you and to speak English like a native? Well now you can . . . with IELO's specialised Jobseeking course. Your IELO teacher will  more...
Conversation English Speak English Online with IELO IELO uses videoconferencing technology so that you talk directly to, or even see, your native English speaking teacher. Conversation Lessons can be 30 minutes or 50 minutes in duration, so you can speak English with your teacher for as long as you want. IELO conversation lessons are informal classes in which our friendly IELO teachers focus on the student's  more...
From KAS Training & Development
Legal Word Processing Course - Microsoft Word 2007 instructor led trainingon-line e-learning cbt (computer based)group study and discussione-booktrain the trainer This comprehensive course focuses on the core formatting elements of Microsoft Word 2003, 2007 or 2010. It provides conceptual and technical learning of the software's advanced features used by international law firm staff to process complex legal documents. The KAS Training Legal Word Processing course was developed by legal trainers with more than 20 years of experience in the legal industry.  more...
Word Processing for Law Professionals Webinar - featuring Microsoft Word 2007 The Principles of Legal Word Processing The Fundamentals of Microsoft Word The Perils of Direct Formatting From WordPerfect to Microsoft Word Styles: The Backbone of Document Formatting  more...
From Webucator
MOC 8824 - Sales Order Processing in Microsoft Dynamics GP 10.0 ...customer ' s order from the initial quote to the shipment documentation and final invoicing. You learn how to perform additional functions setting up process holds for quality assurance and linking order documents to purchase orders.A thorough understanding of these topics allows you to boost sales order processing productivity and help improve customer service by automating sales order  more...
Advanced JavaScript With Prototype and Script.aculo.us In this Advanced JavaScript course, students learn to write production-grade JavaScript using object-oriented programming techniques, good standard coding conventions. Student will learn to catch errors, debug and test, and properly document code with JSDoc. This class also covers Prototype and script.aculo.us.  more...
Windows 7, Enterprise Desktop Support Technician This Windows 7 training class provides students with the knowledge and skills needed to isolate, document and resolve problems on a Windows 7 desktop or laptop computer. It will also help test takers prepare for the 70-685 exam.This class is intended for Windows 7 desktop support technicians who resolve Tier 1 and 2 problems on desktop computers.  more...
Programming Microsoft Office SharePoint Server 2007 This SharePoint training course focuses on the enterprise features of MOSS and how to extend them. You will learn how to customize SharePoint ' s document policy feature and add your own actions. You will gain guidance on how to work programmatically with the Records Center, Content Management, Search Center, and InfoPath Services. You ' ll learn to extend the document converter functionality with  more...
Managing Performance Training This Managing Performance training course teaches students the basics of creating a performance plan and the appraisal process. Students will learn how to conduct a performance-planning meeting, document the performance plan, provide positive and constructive feedback, coach employees during the appraisal period, appraise employee  more...
From Manufacturing Executive Institute
How to Dramatically Improve the Quality of Your Shipment ForecastsTechniques to Improve Forecast Inputs ...on goes into a a Market Requirements Definitiona (MRD) document and how it should be created and maintained. 4. Learn how to better use past shipment data to more closely predict future shipments. 5. Learn the importance of acquiring current (or real-time), data in order to make appropriate short-term forecast adjustments. Participants in this montha ™s important one-hour 3rd  more...
From GlobalCompliancePanel
Risk Assessment - Compliance Using Easy To Fill Out Documentation - Webinar By GlobalCompliancePanel This webinar teaches how to determine and document risk in a process in order to reduce validation time and ensure compliance. Tuesday, February 21, 2012 10: 00 AM PST | 01: 00 PM EST  more...
FDAs Revised Draft Guidance on Medical Device Changes and the 510k - Webinar By GlobalCompliancePanel This webinar will discuss the new draft guidance document from the FDA: "510(k) Device Modifications: Deciding When to Submit a 510(k) for a Change to an Existing Device", dated July 27, 2011. Wednesday, January 25, 2012 10: 00 AM PST | 01: 00 PM EST  more...
A Practical Look at Discipline and Termination - Webinar By TrainHR ...deciding: when and what kind of discipline to use, how to document it, and how to implement it. Importantly, you'll also look at how your own conduct can contribute to performance management problems on your teams. In addition, you'll learn about the need to view and position discipline as a positive tool rather than as an oppressive or punitive one. The webinar will also review some best  more...
Document Approval Control and Distribution How to Meet FDA QSR and ISO 13485 Requirements in a Cost Effective Manner - Webinar B This webinar will provide valuable assistance to all regulated companies, since a CAPA program is a requirement across the Medical Device, Diagnostic, Pharmaceutical, and Biologics fields.  more...
CAPA Failure Investigation and Root Cause Analysis to Meet FDA Expectations - Webinar By GlobalCompliancePanel Defined Failure Investigation and Root Cause Analysis is a major tool in product complaint, non-conformance, and OOS failure investigations, and hazard analysis / risk management and mitigation activities, the basic foundation of a viable CAPA system. Wednesday, November 16, 2011 10: 00 AM PDT | 01: 00 PM EDT  more...
Use and Mis-use of FMEA in Medical Device Risk Management - Webinar By GlobalCompliancePanel This webinar will update personnel at medical device companies on the ISO 14971 standard and point them to the additional information available in the document under the informative annexes. The information will assist in meeting various national and global regulatory requirements for medical devices.  more...
From ZaranTech.com
SAP FICO Online Competency Development Training program ...f Chart of Accounts/ Account Group 5. Retained Earnings/ Document number ranges/ Document Type/ Document Posting 6. New General Ledger 7. G/ L account creation/ change/ display/ blocking & unblocking/ balance display 8. Document display/ change/ changed documents display/ holding/ parking/ reversal 9. individual/ mass/ accrual /deferral cleared item reversal 10. Sample/ recurring  more...
From GlobalCompliancePanel
A Simpler Approach to Implementing or Validating CGMPs to 21 CFR 11 Electronic Records Signatures - Webinar By GlobalComplianceP ...Q9 Product Risk Management models, to structure, run, and document acceptable cGMP Part 11 software validations. The FDA and other regulatory agencies have stated that software validation can realistically only be accomplished effectively if "risk-based". How can this be accomplished in the "real world". This webinar will address software that is supporting the company's Quality System and  more...
Effective Hazard Analysis to meet FDA and ISO134852003 Risk Management Requirements - webinar by global compliance panel FDA-GMPs, known as Quality System Regulations (QSRs), and ISO 13485 require Risk Management as integral part of the development life cycle.  more...
HIPAA and Security Breaches Most frequent issues and causes and trends for future threats by GCP The HIPAA Breach Notification Rule has been in effect since September 23, 2009 and most organizations are not prepared to respond to a breach of PHI and report and document it properly. We will discuss the origins of the rule and how it works, including interactions with other HIPAA rules and penalties for violations  more...
Risk Assessment - Compliance Using Easy To Fill Out Documentation BY GCP This webinar teaches how to determine and document risk in a process in order to reduce validation time and ensure compliance  more...
Document Retention and Destruction ...iance. Effective Human Resource Departments should have a documented Plan to manage employee records safely and effectively. Why should you attend: In order to be in compliance with recordkeeping compliance you should review your policies and practices on record retention and destruction on a regular basis. This webinar will cover federal record-keeping requirements for confidential and  more...
How to Create Configure and Manage a Design Inputs - Design Outputs Traceability Matrix utilizing the principles of Lean Documen ...n and maintenance of duplicate information across various documents - a major source of errors. This webinar applies the Theory of Lean Documents and the corresponding Theory of Lean Configuration to avoiding these errors, while presenting a fresh new approach to these key and related documents. Why you should attend: Do you find yourself constantly struggling to create, manage, and maintain  more...
Creation and management of a Controlled Document System for a Life Sciences manufacturing plant utilizing the principles of Lean ...documents are one of the foundational building blocks of a Quality Management System (QMS) for regulated industries. Too often, controlled documents are cluttered, confusing, and cause many errors due to the way they are created, organized, and managed. This webinar applies the Theory of Lean Documents and the corresponding Theory of Lean Configuration to this key part of a QMS. Why you  more...
Creation and configuration of a Equipment Facilities and Preventive Maintenance System utilizing the principles of Lean Document Proper preventive maintenance and management of process equipment, and facilities is the foundation for any manufacturing process, including many processes not typically thought of as manufacturing.  more...
Creation of DHFs DMRs and DHRs utilizing the principles of Lean Documents and Lean Configuration by GlobalCompliancePanel Design History Files (DHF), Device Master Records (DMR), and Device History Records (DHR) are key building blocks used in the design, development, manufacturing, and cGMP compliance for the Medical Device Industry. Too often, these are cluttered, confusing, and cause many errors due to the way they are created, organized, and managed. This webinar applies the Theory of Lean Documents and also  more...
Document Retention and Destruction by TrainHR You should attend this webinar to be sure both you and your staff in charge of records understands the responsibility and importance of knowing and following proper procedures. When auditing how information is kept by Human Resource Departments, many questions come up regarding where records are kept, how long they should be kept and when and how they should be destroyed in order to stay in  more...
Understanding and Implementing USP 1058 Analytical Instrument Qualification - Webinar By GlobalCompliancePanel Analytical instruments should be qualified to demonstrate suitability for the intended use. Despite the fact that instrument qualification is nothing new and companies spend a lot of time, it is a frequently cited deviation in FDA inspectional observations and warning letters. Companies are unsure on what exactly to qualify or re-qualify, test and document. The main reason is that unlike for  more...
Good Documentation Practices for Laboratory Operations - Webinar By GlobalCompliancePanel ...Part 211 and Eudralex, Volume 4) requires the use of good documentation practices. These practices apply to all pharmaceutical manufacturing and support areas. Good Documentation Practices describe the required activities and steps to use when recording data and other handwritten entries. Personnel, who work with documentation must be informed of these requirements, recognize their significance  more...
Information Security and Payment Card Rules Protecting Patient Payment Data and Complying with PCI - Webinar By GlobalCompliance ...ltiple regulatory requirements and will learn the role of documentation in showing compliance and assisting in the information security management process. Having good policies provide the foundation of good practices and compliance - we will discuss a set of topics that should be covered in a good set of information security policies meeting HIPAA and PCI requirements. Areas Covered in the  more...
Develop and Execute the Company Software VV Program - Webinar By GlobalCompliancePanel ...Q9 Product Risk Management models, to structure, run, and document acceptable software validations. The FDA and other regulatory agencies have stated that software validation can realistically only be accomplished effectively if "risk-based". How can this be accomplished in the "real world". This webinar will address software that is: * As-Product * In-Product * In Production  more...
Root Cause Analysis - The Heart of a Successful CAPA Program - Webinar By GlobalCompliancePanel ...ing * A Suggested Investigation Template * ID / Document the Problem * Investigation / Analysis Methodology - The 7 RCA "Tools" * Find the Solution(s) * Monitor for Effectiveness * Lock In the Change - Close the Loop * Take It to the Next Level Who will benefit: * Senior management in Drugs, Devices, Biologics, Dietary Supplements * QA * RA  more...
Design History File DHF Device Master Record DMR Device History Record DHR and Technical File TF - Regulatory Documents Explaine ...Overview: This Webinar is designed for people involved in document preparation and maintenance, and those who have involvement with documentation. The FDA QSR and the Medical Device Directive specify certain documents or records that should be included in your organization's quality systems - Design History File (DHF), the Device Master Record (DMR) the Device History Record (DHR), and the  more...
The Most Common Problems in FDA Software Validation Verification- Webinar By GlobalCompliancePanel ...nderstand the applicable regulations and solid methods to document compliance. * FDA inspectors are now being trained to evaluate software validation practices. * Increasing use of automated manufacturing and quality systems means increased exposure. * Most recalls can be traced back to computerized equipment, exposing the validation process to scrutiny. * A third of recent  more...
FDA Clinical Trial Auditing and the due diligence Companies should conduct as part of their monitoring program - Webinar By GCP ... this is ethical research. To not follow the protocol and document study conduct carelessly is folly. Why should you attend: All CRO's, Sites, and Sponsors of Clinical Research involved in the drug and device development process have an interest in being prepared for the audit process. Attending this Webinar is a good step toward learning the FDA processes and why the Sponsor's / CRO's  more...
Calibration and Qualification in Analytical Laboratories - Webinar By GlobalCompliancePanel ... Companies are unsure on what exactly to qualify test and document. For easy implementation, attendees will receive: * 4 SOPs o User Requirement Specifications (URS) for analytical equipment o Change control for analytical equipment o Qualification of equipment o Allocating Analytical Instruments to USP Categories * Allocating  more...
Good Documentation Practices for GMP Operations - Webinar By GlobalCompliancePanel ...g or doubtful data, laboratory employees must follow good documentation practices. According to the FDA, if it isn't written down, it didn't happen. As well, if it isna ™t written down clearly, it didna ™t happen either. GMP compliance (21CFR, Part 211) requires the use of good documentation practices. These practices apply to all pharmaceutical manufacturing and support areas.  more...
HIPAA Breach Notification What to do to prevent breaches and what to do when they happen to you - Webinar By GCPanel ...not prepared to respond to a breach of PHI and report and document it properly. We will discuss the origins of the rule and how it works, including interactions with other HIPAA rules and penalties for violations. * HIPAA Covered Entities and Business Associates need to know where and what information they have, so they can know if there has been a breach, and figure out how serious a  more...
Regulatory Complaint Handling Vigilance Recalls - Webinar By GlobalCompliancePanel ...n the USA, EU & Canada. Suggestions for investigating and documenting complaints & pitfalls will be included. Areas Covered in the Session: * Complaints Definitions; FDA, EU & Canada * How to Document Complaints & Adverse Events * US & Foreign Regulatory Reporting * Recall, Vigilance, Correction & Removals * Enforcement Actions Who Will Benefit: *  more...
Developing the Risk Management Plan - Webinar By GlobalCompliancePanel ...ical methods for meeting the requirements. Examples of documentation of the Plan will be presented, including Risk Acceptability Criteria, risk review, verification activities, and information collection activities. While Risk Management Plans can be part of the Quality Plans for a product, important characteristics of the Risk Management Plan must be documented to meet requirements. In  more...
Efficient Computer System Validation - 10 Easy Steps - Webinar By GlobalCompliancePanel ...ar details all of the templates used to create validation documentation, usually saving two-thirds of the time and costs. The 10-step risk-based approach to COTS software validation minimized documentation and ensures efficient implementation of new and upgraded computer systems. This experience will prepare you to perform a validation project. Areas Covered in the Session: * Learn  more...
From Learningdom
XML Training instructor led trainingon-line e-learning cbt (computer based)coursewarebookcomputer lab ...rowsers Editing XML files Free XML editors 5. XML DOCUMENT STRUCTURE Sample XML document XML Tree XML Syntax Comments in XML Special characters Parts of an XML document XML Prolog 6. XML FAMILY TREE What is XML Family tree? Tree rules XML Ancestor and XML Descendant XML Parent and XML Child XML Sibling 7. ELEMENTS & ATTRIBUTES What is an element?  more...
From GlobalCompliancePanel
Developing and Using the Product Risk Management FileReport - Webinar By GlobalCompliancePanel ...for meaningful hazard analysis, hazardous conditions, and documentation have always existed by regulatory agencies. There is an increased awareness of the importance of design activities to support the production of safe and effective product. Product risk management is a required tool to drive and direct resource constrained product design, manufacture and validation activities in the  more...
Change Control -- Your Companys GMP Weak Point - Webinar By GlobalCompliancePanel ... / FDA 483 a Hot Buttonsa * Design Control * Document Control * Identifying changes * Preventing negative changes * Maintain a 'state of control' * Business needs and obtaining 'buy-in' Who Will Benefit: * Senior management in Drugs, Devices, Biologics, Dietary Supplements * QA * RA * R&D * Engineering * Production *  more...
Excel Spreadsheets and FDA Device Regulations - Webinar by GlobalCompliancePanel ... the requirements for a validation plan. The FDA Guidance document, General Principles of Software Validation, has a section devoted to this kind of software application. The seminar explains FDAa ™s thinking and shows how to follow the guidance document. Lastly, we look at the electronic record aspects of the spreadsheet. 21 CFR 820. 180 provides General Requirements for records. Part  more...
Process Validation current industry practices and FDA Guidance Document Review - Webinar by GlobalCompliancePanel ...current industry practices. The recent draft FDA Guidance Document on process validation will be reviewed and case studies will be presented that will allow the attendee to see practical examples of process validation protocols. Areas Covered in the Session: * Recent Guidance Documents * Industry Practices * Examples of Process Validation Protocols * What should be  more...
Understanding the Technical Requirements of 21 CFR Part 11 - Webinar by GlobalCompliancePanel ...the Session: * Leveraging a Part 11 Interpretation document * The Importance of Part 11 in Requirements and Specifications documents * The Role of Risk Assessment in Part 11 Compliance * Technical Controls for Electronic Records * The Many Flavors of Audit Trails * Open vs. Closed Systems * Technical Controls for Electronic Signatures * Handwritten vs.  more...
Validating Excel and Word Applications Documents - Webinar By GlobalCompliancePanel ...ing steps are expected under the CGMPs and other guidance documents for such apps software? How can these consistently be executed? Where does ISO 14971, ICH Q9, and similar risk management systems come in? This webinar will evaluate the climate that has resulted in this call for change, and flag areas for heightened compliance in V&V planning. It will focus on eliminating major systemic  more...
Effective Training Practices for FDA Compliance - Webinar By GlobalCompliancePanel ...esponsible for training, training effectives and training documentation. By examining the GMP expectations on training from different regulatory bodies (from the regulations and citations), attendees will be able to envision what to include in a GMP training program. In addition, an overview of the training system, including types of training planning, will offer considerations to make GMP  more...
Avoiding FDA 483 Observations by Identifying the Root Cause of Deviations - Webinar By GlobalCompliancePanel Overview: Recent Consent Decrees have included requirements that the firm develop and implement systems that result in timely and complete investigations of deviations and corrective and preventive actions that address the root cause of deviations. FDA 483 and Warning letter observations identify inadequate investigations and follow-up. This webinar addresses adequate investigation of  more...
Design History File DHF Device Master Record DMR Device History Record DHR and Technical File TF - Regulatory Documents Explaine ... FDA QSR and the Medical Device Directive specify certain documents or records that should be included in your organization's quality systems - Design History File (DHF), the Device Master Record (DMR) the Device History Record (DHR), and the Technical File (TF). Do you know what information should reside in a DHF, a DMR and a DHR? This Webinar will define, explain and clarify the different  more...
Validation and Use of Excel Spreadsheets in FDA Regulated Environments - Webinar by GlobalCompliancePanel Excel Applications are widely used in laboratories, offices and manufacturing e. g., for data capture, data manipulation and report generation. Regulations such as HIPAA, Sarbanes Oxley Act and FDA's GxP and 21 CFR Part 11 require users of software and computer systems to demonstrate and document data accuracy, integrity and confidentiality. Out-of-the box Excel has not been designed for  more...
Complaint Handling in Compliance with FDA and ISO Regulations - Webinar by GlobalCompliancePanel ...documenting, and implementing a complaint-handling system, including the requirements for complaint review, investigation, and corrective action, as well as the ISO-specific implications. This session will discuss the best way to document customer feedback, what constitutes a complaint, and what do with "non-complaint" feedback. Also contained will be a suggested method on including  more...
Training Requirements and Practices to Assure QSR and ISO Compliance - Webinar by GlobalCompliancePanel ...luding new employee training, methods of training, how to document training so that it is readily available for review (by managers, auditors or inspectors), when to evaluate training requirements, training effectiveness, and when training is not required. Why Should You Attend: On of the easiest ways to be cited for a major noncompliance during an ISO audit is to have an insufficient  more...
GMP Expectations for Products Used in Early Phase IND Studies - Webinar by GlobalCompliancePanel ...document covering GMP requirements for Phase 1 products. These guidelines remove some of the problems that are encountered with early phase products and are in addition to those that cover the CMC sections for IND submissions at Phase 1. Although the guidance appears to remove the need to follow GMPs for Phase 1 products, the need to follow GMPs is still present in the Food, Drug, and  more...
Medical Device Classification - Webinar by GlobalCompliancePanel In 1976, the FDA received authority to regulate medical devices. The plan, written into law, establishes three risk classes for devices (I, II, and III). The three risk levels require different types of control. The webinar explains the two dimensional sy The EUa ™s MDD classifies devices using a rule based system found in Annex IX of the MDD. Devices fall into four risk categories (I,  more...
Statistical Concepts of Process Validation - Webinar by GlobalCompliancePanel ...tatistical concepts. The Global Harmonization Guidance document on process validation shows the application of statistical techniques. In particular, the guidance explains the use of design experiments (DOE) to establish process parameters and develop challenge points for the Operational Qualification (OQ) phase. The guidance explains the concepts of process capability showing the  more...
Document Approval Control and Distribution How to Meet FDA QSR and ISO 13485 Requirements in a Cost Effective Manner - Webinar b ...Document control can be a time- and paper-consuming process. Even the simplest of changes often requires an inordinate amount of time spent in the preparation, submission, distribution, and implementation of change requests, document modifications, document review meetings, document approvals, and document placement. Many companies can spend MUCH LESS time and prepare MANY LESS documents,  more...
Robust Process Validation for Medical Devices - Webinar by GlobalCompliancePanel One of the most common reasons noted by the FDA for recalls of medical device is improper validation. It is also one of the most common reasons companies receive 483s and warning letters. Conversely, successful validations not only satisfy compliance and regulatory requirements, they also provide for robust manufacturing processes satisfying the needs of many individual functions within your  more...
Outsourced processes and ISO 90012008 - Webinar by GlobalCompliancePanel ... To help clarify the requirements, ISO issued a guidance document on Outsourced Processes. The presentation explains the changes to ISO 9001, and recommendations in the guidance document. We take a practical implementation approach, showing how to evaluate and select outsource suppliers, especially service suppliers. We develop methods for written supplier agreements, which define controls  more...
Regulatory Requirements for Medical Device Calibration Programs - Webinar by GlobalCompliancePanel ...equirements, the presentation examines available guidance documents. The FDA issued the Medical Device Quality Systems Manual to help companies implement the Quality system Regulation. Chapter 7 discusses the role of calibration systems in the QMS and helps define the regulatory expectations. ISO 10012: 2003 Measurement management systems - Requirements for measurement processes and  more...
A Guide for Compliance with Document Control Requirements for Food Manufacturers - Webinar by GlobalCompliancePanel An essential part of the Food and Site Security Plan and the Bioterrorism Act. of 2002 section 306. The control of food safety and quality records as required by customers, regulators and internal audit and legal disciplines.  more...
Best Practices in Complaint Management - Compliance Webinar by GlobalCompliancePanel ... This session will include the requirements for defining, documenting, and implementing a complaint-handling system, including the requirements for complaint review, investigation, and corrective action, as well as the ISO-specific implications. This session will discuss the best way to document customer feedback, what constitutes a complaint, and what do with "non-complaint" feedback. Also  more...
From McCord and Associates
Creating a Career Changing Personal Marketing Plan Workshop Series on-line e-learning cbt (computer based)workshop / seminartele-workshop series ...document that sets out in detail exactly the marketing channels that will be attacked and marketing methods that will be used; creates each marketing piece; identifies exact past history production percentages and ratios; makes projections based on past history; identifies problem areas and sets out a detailed plan to correct them; establishes objective goals with specific timelines; and  more...
From Strategic Agile Technologies
Complete Java Training ...X and DOM o The Simple API for XML (SAX) Parser o The Document Object Model (DOM) Parser * Core Java Application Development training with Exercises JDBC Data Access * Introduction to JDBC o The JDBC API o Connecting to the Database o Creating a SQL Query o Getting the Results o Updating and Insert operations * Statements and Prepared Statements o Executing SQL  more...
From e2e Projects Pvt. Ltd
Microsoft Enterprise Project Management Consulting Major services: With expertise in the information technology and project management space, we can provide high quality solutions; on time and on budget. a Enterprise Project Management Solutions a Enterprise Portfolio Management Solutions a Program Management Office (PMO) Setup a Document Management Solutions a Timesheet Management Solutions a SharePoint Server Solutions a  more...
From TrainHr
Bulletproof Documentation HR Supervisor Manager Training - Webinar By TrainHR In our litigious society, it has become more & more important for supervisors to know how to document & discipline employees to avoid law suits and manage employee performance effectively.  more...
From Consepsys Information Management
Document Control Training A comprehensive and hands-on document control training course, covering all aspects of document control tasks. Specialized in Oil and Gas, Energy, Engineering Projects and Construction sectors.  more...
From Keen Info Solution
Online Training for SAP QM with 6years Real Time Expert on-line e-learning cbt (computer based) ... Processing a Define Delivery Block Tables a Define Document Types Tables a Define QM Systems a Define Status of Supply Relationships a Solution for wrong confirmation and wrong usage decision(UD) a Calibration of test equipment a Vendor Blocked for Quality Reasons a Adding Extra Field On Notification a Batch Management a Batch Classification Configuration a QM  more...
Oracle Financial R12 Online Training ...pense Journals o Enter User Define Suspense Journals o Document Sequence o Setup Account Aliases o Run Standard Report- Trail Balance a Detail o Run Standard Report - Translation Trial Balance o Run Revaluation o Auto Posting Journals o Auto Reversal Journals o Enter Recurring Journals o Enter Inter Company Journals o About Security Rules o About Cross Validation Rules o Run  more...
Online Training for Oracle RAC DBA with 6y Real Time Expert Oracle a RAC Course Contents: Day 1: Unit1 Introduction and installation Advantage of using RAC Architecture of RAC Cache fusion, Multi instance transaction behavior Extra background process in RAC Day 2: Unit -2 Oracle RAC 10G installation Pre-requisite before installation Unit-3 Clusterware installation ASM installation  more...
Online Training for OracleApps technical R12 with 6y Real Time Expert ... Profile Option in Oracle Applications. AIM Documentation Preparation. MD 70, CV 60, TE20, MD 120 Reports 6i in Oracle Applications Introduction and Usage of USER_EXITS. Developing a Report from scratch as per Client Requirement. Developing a Report based on MD 50 Document (Reports in GL, AP, PO, INV). Multi-Org Concepts in Oracle  more...
Online Training for Oracle SCM R12 with 6y Real Time Expert ...AIM (Application Implementation Methodology) Overview of Documentations in Real-time Projects Over view of other Service Oriented modules Integrations ORACLE ORDER MANAGEMENT Order to Cash Lifecycle Ordering and Scheduling Process Pricing Process Shipping Process Autoinvoice Process Receivables Process Order Management Process Inventory Organizations and Items Describe  more...
Online Training for Oracle Financial R12 with 6y Real Time Expert instructor led trainingon-line e-learning cbt (computer based)computer lab ...pense Journals o Enter User Define Suspense Journals o Document Sequence o Setup Account Aliases o Run Standard Report- Trail Balance a Detail o Run Standard Report - Translation Trial Balance o Run Revaluation o Auto Posting Journals o Auto Reversal Journals o Enter Recurring Journals o Enter Inter Company Journals o About Security Rules o About Cross Validation Rules o Run  more...
From Business Expert Webinars
E-Mail Communication: Power, Peril, and Protocol ...your next meeting. Your answers will shape a company-wide document creating e-mail protocol. Dr. Julie Miller, founder of Business Writing That Counts!, is an author and business writing expert. Over the past thirty years, Dr. Miller has helped professionals achieve their personal and professional goals by reducing writing time and increasing productivity in email, letter, sales, RFP, and  more...
Process Management for IT & Professional Services Firms ...it process management! IT services firms that do not have documented processes become inefficient, unscalable, and are difficult to manage and they struggle to generate profits. Colette Releford, founder of Strive Business Solutions, a leading process management consulting firm, works with IT professional services business leaders to implement their process management system as part of their  more...
Process Management for Manufacturing & Construction Firms ... process management! Manufacturing firms that do not have documented processes and workflow become inefficient, unscalable, and are difficult to manage and they struggle to generate profits. Colette Releford, founder of Strive Business Solutions, a leading process management consulting firm, works with manufacturing construction leaders to implement process management systems as part of their  more...
Process Management for Manufacturing & Construction Firms ... process management! Manufacturing firms that do not have documented processes and workflow become inefficient, unscalable, and are difficult to manage and they struggle to generate profits. Colette Releford, founder of Strive Business Solutions, a leading process management consulting firm, works with manufacturing construction leaders to implement process management systems as part of their  more...
Process Management for Manufacturing & Construction Firms ... process management! Manufacturing firms that do not have documented processes and workflow become inefficient, unscalable, and are difficult to manage and they struggle to generate profits. Colette Releford, founder of Strive Business Solutions, a leading process management consulting firm, works with manufacturing construction leaders to implement process management systems as part of their  more...
From MicroType
Improve Your FrameMaker Skills on-going series ... HTML outputs. Add interactivity and enhancements to your documentation by inserting hypertext markers for navigation, activation of external files and programs (including e-mail clients and web browsers) and more Mastering Running Headers/ Footers, November 5 (starting 11am PST) Techniques for smart retrieval of information from body pages into running headers/ footers. How to automate  more...
Building a PDF Front-End Interface to Document Collections ...documents -- such as guides, help documents, white papers, technical specifications, spreadsheets, drawings, marketing materials and case studies -- each linked to a different application or accessible in different locations in the directory structure? Would your users appreciate easy access to all these different materials through a single main menu, structured like a web site? Learn how to  more...
Advanced FrameMaker If you are an experienced FrameMaker user, this course will help you hone your skills and work more efficiently. Learn advanced techniques and numerous tips & tricks, including importing content from other formats or documents, automating formatting, editing, graphics, tables, document/ template maintenance, generated files, cross-references, variables, autonumbering, pagination.  more...
From Business Expert Webinars
Measuring the Value of Your Trade Show Program Over 73% of CFOs cite ROI as a critical factor in their evaluation of trade shows Yet, only a small handful of them have the metrics to justify their investment. Marketing programs that don't demonstrate a financial return for the investment are in danger of being cut from the budget. Who is accountable in your company for demonstrating the return on investment (ROI) from your trade show  more...
on-line e-learning cbt (computer based)
online course
 instructor led training
instructor-led class
 study at home
learn at home
 group study and discussion
group study
 self directed
self-directed study
 cd rom
cd-based training
 DVD
DVD video training
 book
printed book
 e-book
e-book digital book
 workshop / seminar
workshop seminar
 train the trainer
train the trainer
 computer lab
computer-based learning
 special pricing!
discount pricing
 on-line tutorial)
online tutorial
Home > Training Search > D > Document > Web-based Seminars
tcw11--02/13/12-20:41:52-(8542)[B]-[A]-[A]