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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
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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