Batch Production Record (BPR) and Device History Record (DHR) Review and...
Batch Production Record (BPR) and Device History Record (DHR) Review and Quality Assessment This webinar will provide the typical elements required to be included in the Batch Production Record and the...
View ArticleThe Form I-9: ICE Storms Could Cost Your Company Millions
The Form I-9: ICE Storms Could Cost Your Company Millions This webinar will explain requirements for filling the I-9 form, including the reverification requirements for non-U.S. citizens and...
View ArticleValidation and Use of Excel® Spreadsheets in FDA Regulated Environments
Validation and Use of Excel® Spreadsheets in FDA Regulated Environments This excel validation training/ webinar will demonstrate how to design spreadsheets for part 11/GxP /SOX/HIPAA, document...
View ArticleFinding Out The Truth in Investigatory Interviews: Falsehoods, Deceptions,...
Finding Out The Truth in Investigatory Interviews: Falsehoods, Deceptions, Omissions and Interference This webinar will cover how to handle the investigatory interviews to find out the truth. The...
View ArticleHow to Develop a Successful ERM Program Ensuring Synergy, Transparency and...
How to Develop a Successful ERM Program Ensuring Synergy, Transparency and System Solutions This webinar highlights the importance of an effective ERM program in project management and risk assessment....
View ArticleRed Flags of Internal Fraud, Asset Misappropriation, and Corruption
Red Flags of Internal Fraud, Asset Misappropriation, and Corruption This webinar will detail the variety of internal economic threats such as fraud, asset misappropriation, and corruption faced by...
View ArticleHow To Transition from Paper to Electronic Records in a Regulatory Environment
How To Transition from Paper to Electronic Records in a Regulatory Environment This webinar will cover effective and efficient ways to transition from paper to electronic records in a regulated...
View ArticleCurrent Good Manufacturing Practices (cGMPs)
Current Good Manufacturing Practices (cGMPs) This webinar will cover in detail the current Good Manufacturing Practices (cGMPs) regulations for pharmaceutical products. Attendees will learn how to...
View ArticleUtility Safety Workshop for OSHA Compliance/Liquid Utilities
Utility Safety Workshop for OSHA Compliance/Liquid Utilities This webinar will provide a comprehensive understanding of the hazard of the liquid utility system. It will discuss in detail hazards...
View ArticleHow to Prepare a Customs Compliance Manual
How to Prepare a Customs Compliance Manual This webinar will explain how to prepare a Customs manual that complies with CBP laws and regulations. Attendees will learn best practices for successfully...
View ArticleEmerging Claims: The Lanham Act, Parallel state law claims and Preemption
Emerging Claims: The Lanham Act, Parallel state law claims and Preemption This webinar will highlight the new and emerging Lanham Act “labeling” claims, Parallel state law claims, the risks and how to...
View ArticleHow to Design and Develop an Effective Reliability Assessment Program:...
How to Design and Develop an Effective Reliability Assessment Program: Methods for Measuring and Reporting Reliability Metrics for Your Verification & Validation Plans This webinar will discuss how...
View ArticleCreating a Global Regulatory Plan
Creating a Global Regulatory Plan This regulatory training will help attendees understand key benefits for implementing and maintaining an effective global regulatory plan. Attendees will also gain...
View ArticleWhy and How - Verification of Compendial Methods
Why and How - Verification of Compendial Methods This webinar will provide an in-depth discussion of USP <1226>, 'Verification of Compendial Methods' requirements. We will discuss FDA 483s on the...
View ArticleAre You Ready for a DCAA Audit?
Are You Ready for a DCAA Audit? This webinar will elaborate the federal contracting process and train attendees on Defense Contract Audit Agency (DCAA) audit guidelines. Why Should You Attend: The DCAA...
View ArticleAre You Ready for a DCAA Audit?
Are You Ready for a DCAA Audit? This webinar will elaborate the federal contracting process and train attendees on Defense Contract Audit Agency (DCAA) audit guidelines. Why Should You Attend: The DCAA...
View ArticleCurrent Good Manufacturing Practices (cGMPs)
Current Good Manufacturing Practices (cGMPs) This webinar will cover in detail the current Good Manufacturing Practices (cGMPs) regulations for pharmaceutical products. Attendees will learn how to...
View ArticleEuropean Filing and Registration Procedures
European Filing and Registration Procedures This Regulatory compliance training is designed to provide an overview of the regulatory environment throughout Europe and will explain how the EU interacts...
View Article510K Table of Contents - Medical Device Description
www.complianceonlie.com ©2010 Copyright © 2014 ComplianceOnline This training session is sponsored by 1 US FDA 510(k): Best Practices for 510(k) Preparation and Submission This Training is Brought to...
View ArticleInformation Required in a 510(k) Submission
www.complianceonlie.com ©2010 Copyright © 2014 ComplianceOnline This training session is sponsored by 1 US FDA 510(k): Best Practices for 510(k) Preparation and Submission This Training is Brought to...
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