Greetings!
There are very few professionals in the pharmaceutical industry who have seen Good Manufacturing Practices from both sides of the table, and even fewer who have spent over four decades doing it.
Terry Pilkey is one of them.
With 44 years across government and industry, she has conducted GMP and Medical Device inspections at Health Canada, worked hands-on in chemical analysis, and gone on to lead regulatory and quality functions at Eurofins Biopharma Product Testing Toronto. Her experience spans the full lifecycle of pharmaceutical products, from development through to compliance, audits, and regulatory readiness.
Today, as Head of Quality and Compliance at AAPS Pharma, she continues to guide professionals through what GMP actually looks like in practice, not as theory, but as decisions, systems, and consequences that play out in real environments. It is one thing to understand GMP requirements. It is another to understand how inspectors think, what they look for, and where organizations typically fall short. That perspective only comes from experience at this level.
Terry will be speaking on April 30.
If you want to understand GMP the way it is applied in the field, this session is worth your time. A 20% discount is currently available using code SAVE20 until April 26. |
No comments:
Post a Comment