Joanna Rapacz

CMC and RA Director & Qualified Person

Joanna brings over 25 years of pharmaceutical industry experience to her role as RA & CMC Director and Qualified Person at QbD Group. Her expertise spans Regulatory Affairs, CMC strategy, GMP quality oversight, and compliance implementation, underpinned by a strong foundation in quality control and R&D. She supports pharmaceutical organisations across the full scope of development and international product authorisation.

1 article

Regulatory AffairsQualification & ValidationQuality Assurance8 may 2026 3 min

EU-GMP Readiness and Supply Chain Strategies for Chinese Pharma

A practical guide for Chinese manufacturers preparing for EU market access. Request the recording to learn how EU-GMP requirements, inspections, and supply chain design impact registration timelines and launch readiness.

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