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The Quality System Regulation (cGMP, 21 CFR 210 & 211 and 820)
July 05 This webinar will examine the 14 key elements of the Medical Device CGMPs, 21 CFR 820, the Quality System Regulation
John E Lincoln John E Lincoln
$249
Raw Material Requirements (Health Canada/USP/EP) in a cGMP Environment - Issues and Solutions Virtual Training
Oct 18-19 The objective of this FIVE HOUR/DAY, ON-LINE two day interactive seminar
Barry A. Friedman Barry A. Friedman
$1,899
cGMP Regulatory Inspections - Through the Eyes of FDA, EMA and PMDA
MP3 Download This webinar will cover the key areas of how ICH Q7 was established, it's goals and objectives, expectations of the healthcare authorities
Kelly Thomas Kelly Thomas
$495
Structuring and Conducting Risk-Based Internal cGMP Compliance Audits
MP3 Download This training will evaluate the chief areas of an FDA cGMP compliance audit and help you understand the actual and anticipated changes
John E Lincoln John E Lincoln
$199
"Zero Defects" and the cGMPs - Pros and Cons
MP3 Download The last few years have seen several major "names" in drugs and devices stumble over quality and cGMP issues, resulting in recalls, lawsuits, and even possible criminal prosecution
John E Lincoln John E Lincoln
$199
Quality Control Laboratory Compliance - cGMPs and GLPs
MP3 Download This course will examine the fundamental requirements for all QC laboratories subject to FDA inspection, recent trends from FDA inspection reports and enforcement actions
Kelly Thomas Kelly Thomas
$1,495
Risk Based Verification and/or Validation to meet US FDA CGMP and ISO 13485 Requirements
MP3 Download This Webinar will provide valuable assistance to all regulated companies that need to review and modify their Master Validation Planning.
John E Lincoln John E Lincoln
$199
Annual Current Good Manufacturing Practices (cGMP) Training
MP3 Download This webinar provides a basic understanding and fundamental principles of Current Good Manufacturing Practices and will fulfill the requirement
Kelly Thomas Kelly Thomas
$229