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Industry:
FDA Compliance
Live
Webinars
[ No Any Live Webinar Found For FDA Compliance Industry! ]
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