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  • fda-import-program-2019-seminar-training
  • ensuring-compliance-with-advertising-and-promotional-requirements-for-drugs-and-medical-devices

Webinars

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Technical and Strategic Considerations in Performing Food Safety Management Systems Gap As ....

  • Mike Weber
  • Jan 24, 2020

The Mindset of an FDA Employee

  • Larry Stevens
  • Jan 27, 2020

New Safe Food for Canadians Regulations

  • Gina Reo
  • Jan 27, 2020

Method Validation under Good Laboratory Practices (GLP)

  • John Fetzer
  • Jan 28, 2020

EU's MDR Effect on U.S. Exports

  • Casper Uldriks
  • Jan 28, 2020

Global Food Additive Regulation Review: Headwinds and Opportunities

  • Carolyn Fisher
  • Jan 28, 2020

Risk Management in Pharmaceuticals and BioTech

  • Martin Lessem
  • Jan 29, 2020

Confidence/Reliability Calculations of Process and Product Capability

  • John N Zorich
  • Jan 29, 2020

Developing a Strategic Approach to FDA Compliance for Computer Systems

  • Carolyn Troiano
  • Jan 29, 2020

Statistical Elements of Real-Time qPCR

  • Elaine Eisenbeisz
  • Jan 29, 2020

Finding and evaluating branded and generic biopharmaceutical market entry opportunities

  • Yali Friedman
  • Jan 30, 2020

Practical Fundamentals for an Effective and Efficient On-the-Job Training Program

  • Mike Kent
  • Jan 30, 2020

Supplier and Service Provider Controls: FDA Expectations

  • Vanessa Lopez
  • Jan 31, 2020

Validation Sampling Plans

  • Alan M Golden
  • Jan 31, 2020

6-Hour Virtual Seminar: Death by CAPA - Does your CAPA Program need a CAPA?

  • Susanne Manz
  • Feb 3, 2020

Performing an Effective, Robust and Compliant Sterility Failure Investigation: How to Avoi ....

  • Charity Ogunsanya
  • Feb 3, 2020

How low can you go? Different ways to determine the limit of detection

  • James Peterson
  • Feb 12, 2020

Pharmaceutical Data Integrity

  • Mark Powell
  • Feb 18, 2020

How Sponsors Generate GCP Noncompliance at Investigator Sites

  • Stephen Schwartz
  • Feb 20, 2020

Seminars

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Ensuring Compliance with Advertising and Promotional Requirements for Drugs and Medical Devices

  • Michael A Swit
  • Boston, MA | June 4-5, 2020

REACH and RoHS Compliance: Gain a Deeper Understanding

  • Kelly Eisenhardt
  • San Diego, CA | February 6-7, 2020

Managing Your Complaints and Obstacles in Post-Market Requirements -- Results from Top Medical Device Observations During an Inspection

  • Rita Hoffman
  • Tampa, FL | February 6-7, 2020

Designing and Sustaining New and Existing Product Stability Testing Program

  • Charity Ogunsanya
  • San Francisco, CA | February 13-14, 2020

HIPAA Privacy Rule Compliance-Understanding New Rules and Responsibilities of Privacy Officer

  • Jim Sheldon-Dean
  • San Francisco, CA | February 26-27, 2020

Reduce costs for compliance with data integrity: 21 CFR Part 11, SaaS/Cloud, EU GDPR

  • David Nettleton
  • Scottsdale, AZ | February 26-27, 2020

Preparing for FDA's New Import/Export Trauma in 2020

  • Casper Uldriks
  • San Francisco, CA | March 19-20, 2020

FDA Recalls - Before You Start, and After You Finish

  • Casper Uldriks
  • San Francisco, CA | March 26-27, 2020

Quality Control Laboratory Compliance - cGMPs and GLPs

  • David L Chesney
  • Boston, MA | April 16-17, 2020

Biocompatibility Testing for Medical Devices

  • Mike Colvin
  • San Francisco, CA | May 7-8, 2020
  • reduce-costs-for-compliance-with-data-integrity
  • quality-control-laboratory-compliance-cgmps-and-glps

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