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Industry: FDA Compliance

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Recorded Session

Fda Compliance And Laboratory Computer System Validation
By: Carolyn Troiano | Recorded Session

Duration: 60 Minutes

FDA's Enforcement Strategy for Mobile Medical Applications
By: J.Lawrence Stevens | Recorded Session

Duration: 60 Minutes

Manufacturing and Marketing OTC Drugs in Compliance with FDA Regulations
By: Dr. Loren Gelber | Recorded Session

Duration: 90 Minutes

Complaint Management: Best Practices to Assure Compliance and Customer Retention
By: Jeff Kasoff | Recorded Session

Duration: 60 Minutes

Data Governance for Computer Systems Regulated by FDA
By: Carolyn Troiano | Recorded Session

Duration: 90 Minutes

Using Learning Management Systems (LMS) to Develop Pharma Training: Rewards & Challenges
By: Michael Esposito | Recorded Session

Duration: 90 Minutes

The FDA Inspection: Preparation, Performance and Follow-Up
By: Jeff Kasoff | Recorded Session

Duration: 60 Minutes

FDA s New Import Program for 2019
By: Casper E Uldriks | Recorded Session

Duration: 60 Minutes

21 CFR Part 11 Conformance for Medical Devices
By: Edwin Waldbusser | Recorded Session

Duration: 90 Minutes

Root Cause Analysis for CAPA - Myths, Challenges, and Best Practices
By: Susanne Manz | Recorded Session

Duration: 90 Minutes

FDA Case Scenarios - Best Practices for Managing Inspection Situations
By: Danielle DeLucy | Recorded Session

Duration: 60 Minutes

21 CFR Part 11 (Electronic Records/Signatures) Compliance for Computer Systems Regulated by FDA
By: Carolyn Troiano | Recorded Session

Duration: 60 Minutes

The 6 Most Common Problems in FDA Software Validation and Verification Computer System Validation Step-by-Step
By: Carolyn Troiano | Recorded Session

Duration: 90 Minutes

Onboarding Employees in a GMP Environment: Best Practices for Foundational Employee Success
By: Michael Esposito | Recorded Session

Duration: 90 Minutes

Implementing an Effective Human Error Reduction Program
By: Ginette M. Collazo | Recorded Session

Duration: 90 Minutes

FDA 21 CFR Part 11
By: Willi Ramseier | Recorded Session

Duration: 60 Minutes

Packaging and Labeling in Pharmaceutical Product Development - Best Practices
By: Michael Esposito | Recorded Session

Duration: 90 Minutes

FDAs Recent Clarification on Guidance for Managing Data Integrity for Regulated Computer Systems
By: Carolyn Troiano | Recorded Session

Duration: 60 Minutes

Bad Standard Operating Procedures (SOPs) - Bad Training: Garbage In, Garbage Out
By: Michael Esposito | Recorded Session

Duration: 90 Minutes

Human Factors Usability Studies Following ISO 62366 and FDA Guidance
By: Edwin Waldbusser | Recorded Session

Duration: 60 Minutes