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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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New MDCG 2020-16 Revision 3 Guidance Documents Released

MDCG 2022-3 Rev.1 released

Revision of MDCG 2019-13 released

New MDCG 2024-16 form released

New MDCG Guidance document released on the implementation of the Master UDI-DI solution for contact lenses

New MDCG Guidance document released

New Q&A released on the gradual roll-out of EUDAMED

EMA launched a new draft guideline on risk management requirements for elemental impurities in veterinary medicinal products

MDCG 2023-3 Rev 1 released

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

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Events calendar

Industry
Service

January

28.01 - 29.01

Clinical

OCT Medical Devices Europe 2025

Munich, Germany

February

02.02 - 06.02

Regulatory Affairs

Medlab Middle East 2025

Dubai, United Arab Emirates

March

11.03 - 12.03

Regulatory Affairs

RAPS Global Regulatory Strategy Conference 2025

Baltimore, Maryland, USA

May

13.05 - 16.05

Regulatory Affairs

RAPS Euro Convergence 2025

Brussels, Belgium
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