Regulatory Updates

The QbD Group regulatory updates blog provides professionals in the life sciences with timely and insightful information on the latest regulatory trends, guidelines, and compliance requirements. Covering topics from pharmaceutical manufacturing standards to medical device approvals, the blog aims to support readers in navigating complex regulatory landscapes, ensuring product safety, and accelerating time to market. Whether you're involved in quality assurance, regulatory affairs, or product development, this blog offers valuable resources to keep you informed and compliant.

Regulatory Updates

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Kirsten Van Garsse, Director AR Services and Manager IVD - RA and Anne Paulussen Senior Consultant IVD - RA

Recent Posts

MDCG 2024-13 and MDCG 2022-5 Rev 1 released

New Q&A on the obligation to inform in case of interruption or discontinuation of supply

Events calendar

May

20.05 - 23.05

EuroPCR: World-Leading Course in interventional cardiovascular medicine

22.05 - 22.05

Symposium on Diagnostic and surveillance of infectious diseases (Sciensano)

27.05 - 29.05

Pharmacy Expo 2025

June

03.06 - 04.06

OCT Medical Devices USA

11.06 - 13.06

EFORT Annual Congress

24.06 - 26.06

CPHI China

26.06 - 27.06

PDA Advanced Therapy Medicinal Products Conference (Europe)

September

07.09 - 11.09

LSI Europe

17.09 - 17.09

Farmaforum

23.09 - 23.09

BioWin day

29.09 - 01.10

TOPRA annual Symposium

October

07.10 - 08.10

World Drug Safety Congress

07.10 - 10.10

RAPS US Convergence

19.10 - 20.10

Annual EU In Vitro Diagnostics Clinical & Regulatory Conference (Q1)

23.10 - 24.10

Team-PRRC Annual Summit

28.10 - 30.10

CPHI Europe

November

17.11 - 20.11

Medica

December

11.12 - 11.12

Dutch Life Science conference