Examples Web-based Seminars

HR 101 WEBINAR SERIES PREVENTING HARASSMENT IN YOUR WORKPLACE The best protection is for managers to understand what their responsibilities are and learn tips to help them prevent harassment in the workplace. This interactive, informative sexual harassment prevention training, "Top 10 Tips for Preventing Harassment in Your Workplace," will provide the tips that managers should not be without. This HR Preventing Harassment Webinar will provide you with the  more...

Top Tips To Prevent Workplace Violence in your Workplace ...h a definition of what constitutes workplace violence and examples of who can engage in workplace violence. It teaches you to recognize the warning signs that can lead to workplace violence and provides techniques and strategies to avoid violence in the workplace. This Workplace Violence Prevention Training makes you aware of situations that may pose a higher risk of workplace violence and  more...

Top Tips For Managers to Prevent Harassment in your Workplace ... work environment sexual harassment. The webinar provides examples from actual court cases. It focuses on an employer's obligations when there has been an incident of sexual harassment as well as strategies on how best to prevent sexual harassment from occurring in the workplace. In addition, this webcast provides an in-depth discussion on other types of unlawful harassment under both federal  more...

Call Center Workforce Management Certification - Live Online - August 1-3 2012 ... any sized organization, large and small, with real-world examples of solutions that work in practice - not just theory. When this learning is expanded to workforce management, the focus extends to forecasts, schedules and budgets. Participants will come to understand the processes that make up the foundation of an effective workforce management practice; the proper ways to gather the right  more...

Call Center Workforce Management Certification - Live Online - April 4-6 2012 ... any sized organization, large and small, with real-world examples of solutions that work in practice - not just theory. When this learning is expanded to workforce management, the focus extends to forecasts, schedules and budgets. Participants will come to understand the processes that make up the foundation of an effective workforce management practice; the proper ways to gather the right  more...

Introduction to Visual Basic 2008 Training ...nt flow control structures. You ' ll work through several examples demonstrating the power of the .NET 3.5 Framework, and dig into creating and consuming your own classes and objects. The course moves on to working with data structures, such as arrays and collection classes, before finishing up with discussions of generics, handling exceptions and working with delegates and events. By the end  more...

Oracle Database 10g: Administration Level II One of the most challenging tasks ever presented to Oracle database administrators is that of recovery from failure, especially if the recovery must not result in a loss of any data. This Oracle trainig class presents all the standard failure scenarios and the best recovery strategies for each. Strategies for on-line backups, complete and incomplete recovery, media recovery vs.  more...

Introduction to C# 2008 Training ...nt flow control structures. You will work through several examples demonstrating the power of the .NET Framework 3.5, and dig into creating and consuming your own classes and objects. The course moves on to working with data structures, such as arrays and collection classes, before finishing up with discussions of generics, handling exceptions and working with delegates and events. By the end  more...

Excel Spreadsheet Validation for FDA 21 CFR Part 11 - GlobalCompliancePanel Overview: This webinar will describe the regulatory and business requirements for Excel spreadsheets, using examples from FDA recommendations. It will then cover the design and installation of those Excel Spreadsheets, to ensure the integrity of the data, and will discuss how to ensure 21 CFR 11 compliance during the development, installation and maintenance of a spreadsheet application.  more...

RAPS Approved Seminar on Risk Management in Medical Devices Industry at Mumbai ...evelopment and maintenance process. It will use real-life examples and proven tips and tricks to make the application of risk management a practical and beneficial undertaking. This seminar will address the system level issues of risk management as well as the increasingly important software related issues of critical systems. It will help to comply with regulatory requirements with minimized  more...

IT Infrastructure and Network Qualification Step-by-Step - Webinar By GlobalCompliancePanel Overview: Federal laws and regulations mandate to put controls and measures on a company network to ensure security and data integrity. Examples are 21 CFR Part 11, Sarbanes-Oxley Act, and HIPAA. With this legislation IT infrastructure and network qualification and compliance become a much more recognizable issue at higher levels of management. Thursday, June 21, 2012 10: 00 AM PDT | 01: 00  more...

Avoiding an FDA Warning Letter with a Strong CAPA Program - Webinar By GlobalCompliancePanel Overview: The development and implementation of an effective CAPA system is not well understood by many device companies. This webinar is designed to clarify what the FDA is looking for in the CAPA system. Examples of warning letters will be reviewed to understand common themes found by FDA. Thursday, March 29, 2012 10: 00 AM PDT | 01: 00 PM EDT  more...

Excel Spreadsheet Validation for FDA 21 CFR Part 11 - Webinar By GlobalCompliancePanel This webinar will describe the regulatory and business requirements for Excel spreadsheets, using examples from FDA recommendations. It will then cover the design and installation of those Excel Spreadsheets, to ensure the integrity of the data, and will discuss how to ensure 21 CFR 11 compliance during the development, installation and maintenance of a spreadsheet application. Tuesday,  more...

Risk Analysis for Portfolio of Drug Development Programs - Webinar By GlobalCompliancePanel Building in strategic risk scenarios into portfolio planning can buffer the organization against the unexpected. Examples might be clinical trial failure, shifts in the marketplace or insufficient resource capacity. This webinar covers various portfolio planning tools and techniques with a focus on strategic risk management. Thursday, February 2, 2012 10: 00 AM PST | 01: 00 PM EST  more...

The Controls for Outsourcing Manufacturing and Testing - Webinar GlobalCompliancePanel ...taining the organization. Outsourcing will be defined and examples throughout the FDA regulated industry will be discussed. Of course, regulatory requirements will be discussed to include the FDA's current thinking about the required controls. Particular emphasis will be given on the importance of understanding the differences between contractors and suppliers. Price List: Live : $245.  more...

Pharmaceutical and Medical Device Good Manufacturing Practices - Similarities and Differences - Webinar By GlobalCompliancePanel This webinar will explore differences and similarities between these GMPs as well as show how they relate to other quality systems, regional regulations, and guidance documents. Examples include ICH, GHTF, ISO particularly ISO 13485 as well as European quality requirements. The considerable use of graphical techniques will enhance this learning experience. Questions are strongly encouraged. Price  more...

SAP FICO Online Competency Development Training program ...ent after each module, a Notes and study material for examples covered. a Access to the Training Blog Training Format: This course is delivered Online using Web and Audio Conferencing. Timing: Weekdays and Weekends after work hours. ABOUT THE TRAINER: a More than 8 years of Consulting & Teaching experience in different modules of SAP FICO. Primarily SAP FI & CO. a With a  more...

JAVA J2EE JEE Professional Role Based Training from Zaran Tech ...ent after each module, a Notes and study material for examples covered. Training Format: This course is delivered as a highly interactive session, with extensive live examples. This course is delivered in Online using Web and Audio Conferencing. Timing: Weekdays and Weekends after work hours. ABOUT THE TRAINER: 1. Worked in various domains like Insurance, Financial / Banking,  more...

SAP BOBJ with BW integration Online Competency Development Training program ...ent after each module, a Notes and study material for examples covered. Training Format: This course is delivered as a highly interactive session, with extensive live examples. This course is delivered in Online using Web and Audio Conferencing. Timing: Weekdays and Weekends after work hours. ABOUT THE TRAINER: a More than 12 years of Consulting & Teaching experience in  more...

Practical Laboratory Statistics This presentation will attempt to remove the fear of statistics that most people share. We will not spend much time on complex equations. Rather, we will focus on the concepts of statistics, and how you can use these concepts to interpret your laboratory results. Our focus will be on using basic spreadsheet functions to compare data sets generated from many different kinds of test equipment.  more...

Preventing Harassment in the Workplace by TrainHR This webinar will concentrate on what is considered sexual harassment as well as covering other types of harassment in the workplace. It will review the laws protecting employees from harassment and the recourses employees have. It will define who is covered and describe the two main kinds of sexual harassment in the workplace. It will cover what should be in an effective Harassment policy, how  more...

Good Documentation Practices for Laboratory Operations - Webinar By GlobalCompliancePanel ...ard expectations of Good Documentation Practices plus see examples of these practices (both good and bad!) as they apply to the pharmaceutical laboratory. Why Should You Attend: Discover what the FDA and EU regulations say about documentation Learn what your signature and/ or initials mean on a document See how to handle and manage data entry and errors Review "Do's"  more...

21 CFR Part 11 How to Successfully Prepare for and Host an FDA Inspection - Webinar By GlobalCompliancePanel Overview: 21 CFR Part 11 is FDA regulation for electronic signatures and electronic records. It started by the pharma - it is a good regulation for medical and pharma companies but it is also a good guideline for other industries. Why Should You Attend: More and more organizations are striving to "go green" and develop "sustainable" organization's strategies, which almost always includes using  more...

Conducting Successful Product Complaint Investigations - Webinar By GlobalCompliancePanel ...APA is tied in to product complaint investigations * Examples of tools currently being used to conduct investigations * How far and in-depth do you go with your investigations * What are current FDA "hot" buttons and trends * Benchmarks and best practices for investigations * How to become a "good" investigator and the emphasis on closed-loop investigations * Why  more...

Data Security Analysis for Healthcare Providers - Webinar By GlobalCompliancePanel ...IPAA and the "meaningful use" rules. It will also provide examples of checklists and questionnaires to assist in uncovering and correcting for data risks and preventing potential HIPAA violations. Why should you attend: Attendees will learn what their risk analysis and security analysis obligations are under HIPAA and the new "meaningful use" rules under the HITECH Act. Attendees will  more...

Good Documentation Practices for GMP Operations - Webinar By GlobalCompliancePanel ... review the Good Documentation Practices plus demonstrate examples of these practices (both good and bad!) as they apply to the pharmaceutical arena. Why you should attend: The Learning Objectives of this presentation include: * Discover what the regulations say about documentation practices * Learn what your signature and/ or initials mean on a document * See how to correct  more...

A Comparison of the Pharmaceutical and Medical Device Good Manufacturing Practices - A Study of Similarities and Differences - W ...y systems, regional regulations, and guidance documents. Examples include ICH, GHTF, ISO particularly ISO 13485 as well as European quality requirements. The considerable use of graphical techniques will enhance this learning experience. Questions are strongly encouraged. Areas Covered in the Session: * Module 1 - Introduction to Quality and Compliance Concepts * Module 2 -  more...

Validation of ExistingLegacy Computer Systems for FDAEU Compliance - Webinar By GlobalCompliancePanel ...n * FDA requirements and inspection practices * Examples of FDA warning letters * Industry recommendations, e. g., from the GAMP * Assessment activities, e. g., gap analysis and risk assessment * Reviewing and updating the validation master plan for existing systems * Going through the validation lifecycles from planning to ongoing tests in routine use *  more...

Developing the Risk Management Plan - Webinar By GlobalCompliancePanel ...iscuss practical 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  more...

XML Training ...OMPLEX ELEMENTS - BASICS What is a complex element? Examples of complex element Difference between simple and complex element How to define a complex element Various ways of defining a complex element 7. TYPES OF COMPLEX ELEMENTS Empty complex element Definition and examples Complex Types Containing Elements Only Definition and examples Complex Text-Only Elements  more...

Process Validation current industry practices and FDA Guidance Document Review - Webinar by GlobalCompliancePanel ...e 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 included in Process Validation Protocols * The Importance of Good Process Validation * Common mistakes in Process  more...

Practical Laboratory Statistics - Webinar by GlobalCompliancePanel ...ts of jargon and complicated equations. We use real world examples and common spreadsheet functions to show you how to analyze your data. Areas Covered in the Seminar: * Perspectives on statistics * Basic definitions * Hypothesis testing * Evaluating differences in precision - the F Test * Evaluating differences in averages - the t Test * Evaluating real world  more...

Effective Corrective and Preventive Actions CAPA 10 Steps to Success - GlobalCompliancePanel Virtual Seminar - Webinar By Global ...ation + Supporting stories and practical examples of CAPA - when each is appropriate and when one or the other is not appropriate + The regulations and international requirements for CAPA and the clear understanding how to suit your procedures, work instructions and forms to address it * Module 2 o Examples of problem solving tools, management  more...

21 CFR Part 11 Complete Manual For Compliance Success - GlobalCompliancePanel Virtual Seminar - Webinar By GlobalCompliancePanel ...well as during the FDA inspection visit o Some examples of 'shoulds' and 'shouldn'ts' when it comes to the audit trails o Commonly asked questions related to audit trails * NOTE: Throughout the webinar, as a part of the modules above, we will include: o Trends o Warning Letter Examples o Advantages and Challenges of the Regulation  more...

Electronic Raw Data in Regulated Environments - Definition Recording and Archiving - Webinar By GlobalCompliancePanel Overview: All regulations have strict requirements for electronic raw data and other e-records. The objective is to ensure accuracy, integrity, authenticity, security and availability of records during the entire life from generation to deletion. While the intent is the same for all regulations only FDA's 21 CFR Part 11 and the EU equivalent Annex 11 have well defined requirements but still  more...

Understanding and Preparing for FDAs New Part 11 Inspection Program - Webinar By GlobalCompliancePanel ...ies: Implementing Part 11 * Validation templates and examples Areas Covered In the Seminar: * FDA inspections: Preparation, conducts, follow up * Learning from past Part 11 inspections * Scope of the new Part 11 program: time frame, expected outcome * Criteria for selection of target companies * What inspectors are looking for * How to prepare your  more...

Japan - Regulatory Filing Requirements and Compliance Processes for Life Sciences - Part I and Part II - Webinar By GlobalCompli ...regulatory climate will be discussed in depth and several examples will be provided to illustrate effective compliance procedures and techniques. Common issues which have caused difficulties for Life Sciences firms will also be discussed. Course content will also explain how Japan interacts with and utilizes ICH standards and how they relate with other national regulatory agencies. The course  more...

How to Prevent or Handle Protocol Deviations and Violations to be GCP and Regulatory Compliant - Webinar By GlobalCompliancePane Overview: This Webinar deals with what happens, and under what circumstances, when the protocol is not followed (PNF) and why this is of particular significance. Covered, will be how a protocol deviation with the least significant effect where there is no substantive effect on the risks to research participants, no substantial effect of the value or integrity of the data, and did not result  more...

Construct and Manage the Technical File and Design Dossier - Webinar By GlobalCompliancePanel ...n subject to an ISO/ MDD type Audit by the Notified Body. Examples of documents not necessary to be included are Quality Manuals and related lower-level documents. A brief summary of manufacturing processes (flow chart including inspection and preventive monitoring steps) and validation of sterilization processes should be included in the design dossier. Be prepared to review all elements that  more...

Good Documentation Practices in a Regulated Environment - Webinar by GlobalCompliancePanel Whether you work in production or in a laboratory or if you conduct investigations or finalize product release, sound data and information is essential to success and compliance. To ensure success, and avoid those frustrating, embarrassing discussions of missing or doubtful data, employees recognize and must follow Good Documentation Practices (GDP). These practices apply to all pharmaceutical  more...

Combination Products FDAs Proposed Rule for GMP Requirements and Introduction and Expectations for Combo Products - Webinar by G ...examples of combination products? How are combination products assigned for review? Where can I find guidance for how master files can be used in the submission of information relevant to my combination product Determine which Center will review my combination or non-combination product? These topics and more will be addressed during this Webinar, including recently FDA's proposed rule to  more...

Food Traceability Program and Efficacy Verification - Webinar by GlobalCompliancePanel Product traceability requirements for meeting Food Safety and Quality standards as required by BRC fundamental clause 5. 0, SQF item 4. 5, 9 CFR will be covered. The purpose of traceability and its value to the brand will be explored. The resources necessary to achieve an effective result will be presented. A customer perspective on the importance of product traceability from a customer  more...

The FDA Tripod - Clinical Trial Regulations Compliance and GCP in Drug Development - Webinar by GlobalCompliancePanel ...ts receive a foundation of knowledge about GCP, practical examples, and the underlying scientific and regulatory principles involved. Guidelines for each aspect of research are provided, as well as information on the structuring and preparation of protocols, consent forms, and investigator brochure. Information on maintaining ongoing compliance will also be discussed. This course enables  more...

Proper Use of Risk Management Tools for ISO 14971 Medical Device Safety - Webinar by GlobalCompliancePanel ...examples of the use of the tools for medical device risk management to complete the risk management process for a sample medical device. During the presentation we will refer to the risk management standard ISO 14971 and its requirements. We will give examples for completing the documentation requirements of the standard. The presentation is intended to give practical information on  more...

Manufacturing Optimization Online Certificate Program Online training One-hour online sessions meet every Wednesday at 7: 00 p. m. Eastern Time. The Manufacturing Optimization Online Certificate Program consists of three modules covering quality management, root cause failure analysis, and cost reduction and optimization. This training features practical, experience-based and proven approaches for rapidly optimizing your manufacturing process. The  more...

PHP MySql A PHP course designed to enable web developers and others with limited programming experience to build dynamic database driven e-commerce web sites using the PHP programming language. Since PHP is such a rich and task-specific language, the course covers the most important range of functions in depth, and equips delegates to understand the remaining less essential aspects. This is a hands-on  more...

Complete Java Training ...lass will be provided. * Topic discussed with real time examples. * Class exercise * Instructor-led Live training Software required for Training * All the open source softwares are provided as part of Training * A computer with internet connectivity. * Operating system that supports Java 1. 5. 0 or later * Eclipse 3. 2 * My SQL 5. 0  more...