Practical Tips on Hosting an FDA Audit of a Clinical Research Site
Practical Tips on Hosting an FDA Audit of a Clinical Research Site This webinar on clinical trial audits will review the regulations and provide tips for preparing clinical research sites for an FDA...
View ArticlePediatric Drug Development - Relevant FDA Laws and Changing Approach
Pediatric Drug Development - Relevant FDA Laws and Changing Approach This webinar on pediatric drug development will discuss relevant laws and FDA's approach to pharmaceutical and clinical development...
View ArticleHow to Conduct an Internal Audit to Prevent an External One
How to Conduct an Internal Audit to Prevent an External One This webinar will explain strategies for conducting internal audit in an efficient manner. It will provide best practices for payroll...
View ArticleChanges in US FDA Enforcement
Changes in US FDA Enforcement This FDA compliance training will discuss major changes in FDA enforcement and how the regulated industry should respond to any FDA inspection activity. Why Should You...
View ArticleTransforming the Cargo Clearance Process
Transforming the Cargo Clearance Process This Customs and Border Protection compliance training will help the attendees understand the latest CBP developments relating to the entire cargo clearance...
View ArticleAnalytical Method Validation Under Good Laboratory Practices (GLPs)
Analytical Method Validation Under Good Laboratory Practices (GLPs) This analytical method validation webinar will provide provide practical tips on how to validate an analytical method under the GLP...
View ArticleBatch 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...
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