ComplianceOnline
Join for Free
Signin
Welcome back! Please log in below to continue.
Forgot Password?
New customer? Free Signup
Your Shopping Cart
Contains 0items
Total: $0.00
View Shopping Cart
Home ›FDA Compliance ›  Risk Management

FDA Risk Management Regulations Training, Compliance Best Practices and Standards

FDA risk management regulations based webinars, in-person seminars, standards and best practices. Learn from renowned experts about FDA and ISO requirements for risk management in life science products and processes - Risk Evaluation and Mitigation Strategies (REMS), Pharmacovigilance, Safety Compliance and Inspections, Quality risk management, Risk assessment (RA), etc.
Sub Categories: Risk Management | Packaging and Labeling | FDA Audit and Inspection | Drug and Device Approvals | FDA Validation | FDA 21 CFR Part 11 | Marketing and Promotion | Documentation and IT | Quality and Safety | Regulations & Guidances | Best Practices & GXPs
Loading....
Webinar
Excel Spreadsheets; Ensuring Data Integrity and 21 CFR Part 11 Compliance
2
/ Apr
Wednesday-2025

Excel Spreadsheets; Ensuring Data Integrity and 21 CFR Part 11 Compliance

  • Speaker: David Nettleton
  • Product ID: 701582
  • Duration: 75 min
Learn how to use Microsoft Excel spreadsheets for GXP data to ensure compliance with 21 CFR Part 11 and reduce validation cost and time.
* Per Attendee
$229
View Details
Recorded/CD
How to Prepare a Standard Operating Procedure (SOP)?

How to Prepare a Standard Operating Procedure (SOP)?

  • Speaker: Dr. Afsaneh Motamed Khorasani
  • Product ID: 705131
  • Duration: 60 Min
This webinar will detail a step-by-step procedure on how to write a practical, effective and compliant Standard Operating Procedures (SOPs), review and revise SOPs and maintain compliance over the course of the SOP life-time.
CD/Recorded
$199
View Details
Recorded/CD
Human Error Reduction in GMP Manufacturing

Human Error Reduction in GMP Manufacturing

  • Speaker: Ginette M Collazo
  • Product ID: 704107
  • Duration: 90 Min
This training program will offer attendees an understanding of human errors in GMP related environments, factors and causes, and control measures to be put in place to reduce the same.
CD/Recorded
$219
View Details
Recorded/CD
Introduction to Root Cause Investigation for CAPA

Introduction to Root Cause Investigation for CAPA

  • Speaker: Vanessa Lopez
  • Product ID: 704409
  • Duration: 60 Min
This CAPA training program will provide an understanding of FDA and ISO requirements, steps in CAPA process and the challenges associated to root cause analysis. Attendees will learn the tools and quality data sources to use during root cause analysis investigation.
CD/Recorded
$199
View Details
Recorded/CD
Quality Risk Management Overview for Pharma, Biopharma and Combination Products - ICH Q9/ISO 14971

Quality Risk Management Overview for Pharma, Biopharma and Combination Products - ICH Q9/ISO 14971

  • Speaker: Tanvir Mahmud
  • Product ID: 702422
  • Duration: 90 Min
This 90-minute webinar will cover principles and provide examples of tools for quality risk management that can be applied to different aspects of pharmaceutical quality. It will provide you with the knowledge and understanding needed to improve patient safety and also to prepare your organization for regulatory inspections.
CD/Recorded
$299
View Details
Loading....
Best Sellers
PrevNext
You Recently Viewed
PrevNext
Copyright © 2025 ComplianceOnline.com
MetricStream
Our Policies: Terms of use | Privacy