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FDA Compliance

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

By J.Lawrence Stevens
FDA’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 – 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) – Bad Training: Garbage In, Garbage Out
Recorded Session

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

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