Technical Web-based Seminars

Legal Word Processing Course - Microsoft Word 2007 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...

MOC 6292 - Installing and Configuring Windows 7 Client This Windows 7 training class is intended for IT professionals who are interested in expanding their knowledge base and technical skills about Windows 7 Client. In this Windows 7 course, students learn how to install, upgrade, and migrate to Windows 7 client. Students then configure Windows 7 client for network connectivity, security, maintenance, and mobile computing. This course helps students  more...

MOC 5047 - Introduction to Installing and Managing Microsoft Exchange Server 2007 SP1 ...ure and manage a messaging environment in accordance with technical requirements. Students will learn how to install Microsoft Exchange Server 2007 and manage routing, client access, and the backup and restore of databases. They will also learn how to manage addressing and recipient objects such as mailboxes, distribution groups, and contacts.This class is meant for IT Professionals, IT  more...

Java EE Seminar for Managers ...d specifically for non-programmers -- analysts, managers, technical writers, and anyone who desires a good conceptual understanding of Java EE while not needing to drill down into the details of particular APIs or runtime specifications. Developers may also find this course quite useful as a starting point for one or more of our courses in specific Java EE technology -- it gives a great sense  more...

Introduction to Internet Technologies You use the Internet regularly, for both work and personal purposes. But now, for various reasons, you want to learn about the technical side of the Internet: What constitutes the Internet? How is a website developed? What are the emerging trends and technologies on the Internet? In this course, you will examine the technical aspects of the Internet.  more...

Introduction to Microsoft Access 2003 Training ...mental knowledge and techniques needed to advance to more technical Access responsibilities, such as creating and maintaining new databases and using programming techniques that enhance Access applications. It is also for students whose job responsibilities include creating new databases, tables, and relationships, as well as working with and revising intermediate-level queries, forms, and  more...

MOC 5117 - Installing, Configuring, Troubleshooting, and Maintaining Windows Vista This Windows Vista training class provides IT Professionals who work in enterprise organizations with the knowledge and skills to install, deploy, configure, secure, maintain, and troubleshoot Windows Vista. This advanced course is aimed at enterprise desktop support technicians who want to gain an in-depth knowledge of Windows Vista.This class targets experienced IT professionals who focus on a  more...

MOC 5118 - Maintaining and Troubleshooting Windows Vista Computers This Windows Vista training class provides students with the knowledge and skills to successfully maintain and troubleshoot Windows Vista computers.It will provide them with the knowledge and skills necessary to identify technical problems that can occur in an organization  more...

MOC 2778 - Writing Queries Using Microsoft SQL Server 2008 Transact-SQL This Transact-SQL training class provides students with the technical skills required to write basic Transact-SQL queries for Microsoft SQL Server 2008.This Transact-SQL class is intended for SQL Server database administrators, implementers, system engineers, and developers who are responsible for writing queries.  more...

A Case for Routine Use of Statistical Process Control SPC in Manufacturing ... represents a progressive set of predicted and predictive technical tools that any individual can use to diagnose probable causes of predicted process failures and then systematically determine alternative solutions. Most manufacturing company executives, managers, and front-line supervisors have, somewhere in their careers, been to an education event or read a book on the virtues and uses  more...

Design History File DHF Device Master Record DMR Device History Record DHR and Technical File TF - Regulatory Documents Explaine Overview: 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 Technical File (TF). Tuesday, February 14, 2012 10: 00 AM PST | 01: 00 PM EST  more...

DHF DMR DHR and the Technical File-Design Dossier - Similarities and Differences - Webinar By GlobalCompliancePanel This webinar will examine the existing and proposed requirements for the FDA's DHF -- including its derivative documents, the DMR and DHR. Wednesday, March 7, 2012 10: 00 AM PST | 01: 00 PM EST  more...

The DHF DMR DHR and the Technical File Design Dossier - Regulatory Requirements - Webinar By GlobalCompliancePanel This webinar will examine the existing and proposed requirements for the FDA's DHF -- including its derivative documents, the DMR and DHR. Wednesday, November 2, 2011 10: 00 AM PDT | 01: 00 PM EDT  more...

JAVA J2EE JEE Professional Role Based Training from Zaran Tech ...n IT projects as Sr. Architect, Lead Developer / Analyst, Technical Manager. 3. Extensive CRM experience with various projects 4. Trained & mentored more than 250 people in US, Europe and South East Asia 5. Worked with global clients and teams (US, Germany, UK, Japan, Dubai, Qatar, India) 6. Helped set up the EA Team and put together the standards and templates for the organization 7.  more...

This Webinar will provide a substantive overview and outline differences between the Technical File and Design Dossier for those This Webinar will provide a substantive overview and outline differences between the Technical File and Design Dossier for those device firms dealing with the global regulatory landscape.  more...

Design History File DHF Device Master Record DMR Device History Record DHR and Technical File TF - Regulatory Documents Explaine This webinar will provide valuable assistance to all device manufacturers, those who market solely within the US, or those who wish to market in the EU as well  more...

Winning Presentation Skills Put Power Punch and Pizzazz into Your Presentations by TrainHR If you want to project poise and professionalism, captivate your listeners, persuade people to act on what you say and develop comfort and confidence this session is for you.  more...

DHF DMR DHR Technical File and Design Dossier - Key Requirements and Future Directions - Webinar By GlobalCompliancePanel ...fferences; Future trends; Typical DHF Table of Contents; Technical File or Design Dossier Table of Contents; The importance and usefulness of the "Essential Requirements"; Structure of the "Declaration of Conformity"; self-declaring or N-B reviewed; Parallel approaches to development. Finally, the differing approaches to file audits by the FDA and the Notified Body will be discussed. Why  more...

HIPAA Security Policies and Procedures Making them useful and relevant as well as compliant - Webinar By GlobalCompliancePanel ...onment change. Find out what administrative, physical and technical safeguards are necessary and what policies they call for, and how you decide whata ™s right for HIPAA security compliance for your organization. This teleconference will provide the background and details necessary to develop an understanding of the origins of the HIPAA security regulation and the process used in complying  more...

Information Security Risk Analysis Meeting HIPAA Requirements and the Meaningful Use Objective - Webinar By GlobalCompliancePane ...n Security Risk Analysis Process presented utilizes a non-technical approach, involving interviewing staff knowledgeable about operations and systems to discover how information is retained and moved, and reveal the risks inherent in such storage and transmission. Interview content is organized as departmental stories that are successively refined into process descriptions, lists of information  more...

Recalls Vigilance - When to Report Complaints - Webinar By GlobalCompliancePanel Overview: This webinar will acquaint one with the lessons learned from over 30 years of adverse events and complaints. FDA has issued warning letters for failing to properly evaluate medical device complaints for reporting under 803 & 806 regulations. Vigilance reporting is also required in Canada, the European Union and many other countries. Warning letters and recalls are posted on FDA's  more...

Design History File DHF Device Master Record DMR Device History Record DHR and Technical File TF - Regulatory Documents Explaine ...ter 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 records. Are you maintaining adequate DHF, DMR, DHR, and TF records? Do you know what data and information need to reside and where does it reside? Are your records easily accessible? Are  more...

Conducting Successful Product Complaint Investigations - Webinar By GlobalCompliancePanel Overview: This webinar will provide valuable assistance and guidance to the life sciences manufacturers engaged in various aspects of product complaint investigations. An effective complaint handling system is an extremely important part of any quality system. Manufacturers should understand that any complaint received on a product shall be evaluated and, if necessary, thoroughly investigated  more...

Elements of the Lot Disposition Process - Webinar By GlobalCompliancePanel ... * Compilation of Completed Records * Quality Technical Agreements * QA review of production records * Laboratory Testing Results * Batch Production Record Review * Critical Utilities and Environmental Monitoring Data * Requirements for COA * Communication * Lot disposition Who Will Benefit: * Batch Release personnel * Batch Record  more...

Validating Rapid Microbiological Methods - Webinar By GlobalCompliancePanel ...ize USP Chapter 1223, Ph. Eur. Chapter 5. 1.6 and the PDA Technical Report #33. Areas Covered in the Session: * Learn how to develop a validation strategy * User requirements specifications (URS) * Design Qualification (DQ) * Supplier assessment/ audit * Functional design Specifications (FDS) * Requirements Traceability Matrix (RTM) * Developing test  more...

FDAs Proposed Rule Regarding Device Establishment Registration and Listing and How to Register and List - Webinar By GlobalCompl Overview: Device firms, establishments or facilities that are involved in the production and distribution of medical devices intended for use in the U. S are required to register annually. Most establishments that are required to register with the FDA are also required to list the devices that are made there and the activities that are performed on those devices. FDA issued a 28-page Proposed  more...

Medical Device Recalls How to Manage Them and Recent Trends - Webinar By GlobalCompliancePanel Overview: Medical devices are classified into three classes, Class I, II, and III, based on the level of control necessary to assure the safety and effectiveness of the device. Recalls of Class II devices represent 61% of all device recalls over a review period, followed by Class III devices at 28%. This Webinar will provide a recent update on the latest trends and causes for device recalls and  more...

Information Security - Overview Information security means protecting information and information systems/ assets from unauthorized access, use, disclosure, disruption, modification or destruction. Every individual who deals with information should have a better understanding on how to safeguard his/ her personal or company's data. This session will assist partcipants to 1. Understand WHAT, HOW & WHY of information  more...

Understanding the Technical Requirements of 21 CFR Part 11 - Webinar by GlobalCompliancePanel ...late in the system lifecycle, it is important to give the technical requirements due consideration early in the process. A good understanding of these technical requirements is paramount to avoiding the syndrome of "testing into compliance" later on. Often, the compliance status of a system can be impacted by varying interpretations of the regulation if not properly addressed. This session will  more...

Designing and Implementing the Quality System for Combination Products - Webinar By GlobalCompliancePanel ... Suppliers, and controlling incoming materials Module 7: Technical and "Administrative" Process Controls Module 8: Introduction to Deviations & Quality Failures (0: 10) Module 9: Validation Module 10: Maintaining Label Control-From Design to Label Application Module 11: Storage and Distribution & Returned and Salvaged Products Module 12: Returned and Salvaged Products Module 13:  more...

How to Prepare and Submit a Bullet Proof 510k and Latest FDA Proposed Changes to the Process - Webinar By GlobalCompliancePanel Overview: This 3 hour Webinar is a primer and overview to the premarket notification process, i. e., a 510(k). A 510(k) is a premarket submission made to FDA to demonstrate that your device to be marketed is at least as safe and effective, that is, substantially equivalent, to a legally marketed device that is not subject to PMA. There are three types of Premarket Notification 510(k)s that may  more...

Design History File DHF Device Master Record DMR Device History Record DHR and Technical File TF - Regulatory Documents Explaine ...ter 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 records. Are you maintaining adequate DHF, DMR, DHR, and TF records? Do you know what data and information need to reside and where does it reside? Are your records easily accessible?  more...

Construct and Manage the Technical File and Design Dossier - Webinar By GlobalCompliancePanel ... substantive overview and outline differences between the Technical File and Design Dossier for those device firms dealing with the global regulatory landscape. It is assumed that participants and customers have a prior CE Mark and Medical Device Directive background. The Technical File is a comprehensive collection of information and documents that details everything about your medical  more...

HIPAA Compliance and Workforce Training for Medical Practices - Webinar by GlobalCompliancePanel Training is required in a number of areas of the HIPAA regulations and their policy implementations at medical offices. The HIPAA Privacy Rule includes basic protections of uses and disclosures of protected health information that every staff member must be aware of, from avoiding discussion of patient-related information outside of the office, to taking precautions when faxing information to  more...

Navigating Pediatric Trials from recruitment to successful on-time completion - Webinar by GlobalCompliancePanel Drug companies face many challenges in pediatric clinical research. Pediatric trials come with a high level of complexity and cost. In order for professionals to carry out a successful pediatric drug development plan, they need the right infrastructure and information to avoid obstacles such as slow recruitment, noncompliance and difficulties in developing the right study criteria and protocol.  more...

The DHF Technical File and Design Dossier - Similarities Differences and The Future - Webinar by GlobalCompliancePanel This webinar will examine the existing and proposed requiements for the FDA's DHF and the MDD's TF/ DD. Differing purposes / goals. Differing purposes / goals. Required and desirable contents. Areas requiring frequent re-evaluation / update. Similiarities and differences, and future trends. Typical DHF Table of Contents. Technical File or Design Dossier Table of Contents. The importance and  more...

Pharmaceutical Manufacturing Batch Record Review - Webinar by GlobalCompliancePanel The Learning Objectives of this presentation include: * Recognize regulatory (FDA/ EU) requirements for batch records and batch record review * Modeling best practices of a technical review of batch records * Discover the essentials of batch record reviewer qualifications and training * Acquire confidence in determining the final decision or recommendations. * Establish  more...

Leadership in Manufacturing Contamination Control ...ort for production because it is the hub of the necessary technical expertise. This broad manufacturing support role covers many areas, including routine raw material and product testing, disinfectant/ sanitant qualification, water and compressed gas testing, environmental monitoring, microbiological a awareness traininga of production operators, etc. Perhaps their most difficult leadership  more...

Do I E-Shred This ...ng electronic information. Learn how it's stored (not too technical, I promise!) and where it resides. Learn the 10 privacy principles that form the basis for most privacy legislation and how to use them as part of your or your client's environment. If you or your clients store electronic information, and almost all do, it's critical to include handling e-information as part of the overall  more...

ONLINE TIBCO TRAINING IN HYDERABAD ...ORACLE APPS FINANCIALS SAP PP QA TESTING ORACLE APPS TECHNICAL SAP WM BUSINESS ANALYST ORACLE APPS DBA SAP SRM SAS ABAP WORKFLOW SAP BI JAVA ABAP HR CURRICULUM Added Courses SAP MDM New SQL SERVER SAP IS RETAIL COGNOS DATA STAGE TIBCO TIBCO IPROCESS WEBLOGIC WEBSPHERE PHP RAC IF U WANT ANY ASSISTANCE ON ANY ONE OF THE ABOVE COURSES PLEASE  more...

ONLINE JAVA TRAINING IN HYDERABAD ...ORACLE APPS FINANCIALS SAP PP QA TESTING ORACLE APPS TECHNICAL SAP WM BUSINESS ANALYST ORACLE APPS DBA SAP SRM SAS ABAP WORKFLOW SAP BI JAVA ABAP HR CURRICULUM Added Courses SAP MDM New SQL SERVER SAP IS RETAIL COGNOS DATA STAGE TIBCO TIBCO IPROCESS WEBLOGIC WEBSPHERE PHP RAC IF U WANT ANY ASSISTANCE ON ANY ONE OF THE ABOVE COURSES PLEASE  more...

Complete Java Training ...f you miss any training sessions. * 2 months of free technical support will be provided after training* =========================== Core Java basics. * History and Overview o Structured Programming o Object-Oriented Programming * Java Basics o Java Introduction o Hello Java Program o Compiling and Interpreting Applications o JDK API o Datatypes and Variables o  more...