The Three Sins of GMP Executives

Life Sciences, Pharma Manufacturing & Supply Chain, Pharmaceutical, Pharmaceutical Regulation,
  • Wednesday, January 27, 2016

There are three common sins committed by good manufacturing practice (GMP) executives, each of which usually leads to waste, lost time and compliance issues. Even with renewed efforts to be compliant with FDA regulations, most firms find that they fall short of the goal. The key question is “if we know the GMPs, why do we keep failing?”.

This presentation will discuss the three sins and provide absolution methods on how to be a successful GMP Executive.



Troy Fugate, Vice President, Compliance Insight, Inc.

As the Vice President of Compliance Insight, Inc., Troy works with team colleagues and clients to confirm and facilitate meeting client goals. Troy’s primary strengths are FDA Quality Assurance activities with emphasis in quality systems, risk assessment, facilities and utilities, cleaning, processes, validation and systemic audits. With almost 30 years of experience ranging from foreign audits to consent decree resolution, Troy brings a vast array of knowledge and skills to the discussion.

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Who Should Attend?

Professionals involved in the FDA field and Senior level executives from:

  • Biopharmaceutical Companies
  • Medical Device Companies
  • Compounding Pharmacies

Xtalks Partner

Compliance Insight

Compliance Insight offers hands-on compliance, quality assurance, clinical and regulatory affairs guidance and consulting that is reliable, accurate, timely and supportive of the client’s goals and compliant with US FDA Regulations.

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