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FDA Compliance

Live Webinars
Chronicles

By Carolyn Troiano

Fda Compliance And Laboratory Computer System Validation

Recorded Session

By J.Lawrence Stevens

FDAâ€™s Enforcement Strategy for Mobile Medical Applications

Recorded Session

By Dr. Loren Gelber

Manufacturing and Marketing OTC Drugs in Compliance with FDA Regulations

Recorded Session

By Jeff Kasoff

Complaint Management: Best Practices to Assure Compliance and Customer Retention

Recorded Session

By Carolyn Troiano

Data Governance for Computer Systems Regulated by FDA

Recorded Session

By Michael Esposito

Using Learning Management Systems (LMS) to Develop Pharma Training: Rewards & Challenges

Recorded Session

By Jeff Kasoff

The FDA Inspection: Preparation, Performance and Follow-Up

Recorded Session

By Casper E Uldriks

FDA s New Import Program for 2019

Recorded Session

By Edwin Waldbusser

21 CFR Part 11 Conformance for Medical Devices

Recorded Session

By Susanne Manz

Root Cause Analysis for CAPA - Myths, Challenges, and Best Practices

Recorded Session

By Danielle DeLucy

FDA Case Scenarios â€“ Best Practices for Managing Inspection Situations

Recorded Session

By Carolyn Troiano

21 CFR Part 11 (Electronic Records/Signatures) Compliance for Computer Systems Regulated by FDA

Recorded Session

By Carolyn Troiano

The 6 Most Common Problems in FDA Software Validation and Verification Computer System Validation Step-by-Step

Recorded Session

By Michael Esposito

Onboarding Employees in a GMP Environment: Best Practices for Foundational Employee Success

Recorded Session

By Ginette M. Collazo

Implementing an Effective Human Error Reduction Program

Recorded Session

By Willi Ramseier

FDA 21 CFR Part 11

Recorded Session

By Michael Esposito

Packaging and Labeling in Pharmaceutical Product Development - Best Practices

Recorded Session

By Carolyn Troiano

FDAs Recent Clarification on Guidance for Managing Data Integrity for Regulated Computer Systems

Recorded Session

By Michael Esposito

Bad Standard Operating Procedures (SOPs) â€“ Bad Training: Garbage In, Garbage Out

Recorded Session

By Edwin Waldbusser

Human Factors Usability Studies Following ISO 62366 and FDA Guidance

Recorded Session