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Home ›FDA Compliance ›  Packaging & Labeling Compliance

FDA Packaging and Labeling Regulations Training, Compliance Best Practices and Standards

Life science product packaging and labeling regulations based webinars, in-person seminars, standards and best practices. Learn from renowned experts about FDA regulations for packaging and labeling life science products - Fair Packaging and Labeling Act, Cosmetic Labeling and Label Claims, Food Labeling Guide, Nutrition Labeling, 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
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Recorded/CD
Implementing a Bullet Proof Quality System for FDA Audit Success

Implementing a Bullet Proof Quality System for FDA Audit Success

  • Speaker: Meena Chettiar
  • Product ID: 705400
  • Duration: 60 Min
This webinar will provide an overview of the FDA expectations in medical device industries for setting up a quality system for FDA audit readiness. It will also provide an understanding of the quality system inspection techniques (QSIT) requirements for documents controls, production and process controls, packaging and labeling controls and more.
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Recorded/CD
Understanding FDA Import Alerts: What Are They and Recommendations For Removing Your Company And Products From An Alert

Understanding FDA Import Alerts: What Are They and Recommendations For Removing Your Company And Products From An Alert

  • Speaker: Karl M. Nobert
  • Product ID: 703313
  • Duration: 90 Min
This webinar provides attendees with an introduction to FDA Import Alerts and what they are, examine why they are issued, show you where to locate them and how to determine whether a company or product is on one, and finally, provide strategic recommendations for removal from an alert.
CD/Recorded
$349
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Recorded/CD
FDA Regulations for Marketing OTC Drugs and New Legislation

FDA Regulations for Marketing OTC Drugs and New Legislation

  • Speaker: Norma Skolnik
  • Product ID: 704145
  • Duration: 60 Min
This training program will illustrate why it’s essential to understand FDA regulations and OTC labeling requirements to market OTC drugs in the U.S.
CD/Recorded
$249
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Recorded/CD
Classifying Medical Devices - US and EU

Classifying Medical Devices - US and EU

  • Speaker: Charles H Paul
  • Product ID: 705045
  • Duration: 60 Min
The Medical Device Classification webinar explains the classification system in US and the EU.
CD/Recorded
$219
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