top of page
GRRO European Union
GRRO EUROPE
The GRRO Europe Subgroup proactively develop collaborative relationships with various stakeholders in Europe, including EMA, national regulatory agencies, pharmacopeia, other standard-setting bodies, pharmaceutical industry, suppliers and other trade groups. GRRO Europe stays abreast of, and seeks to scientifically impact, regulatory developments for OINDPs in Europe.
News
28 August 2019
Consultation on the application of Analytical Quality by Design concepts to pharmacopoeial standards for medicines
23 August 2019
Comments to EMA ‘Guideline on the quality requirements for drug-device combinations' (EMA/CHMP/QWP/BWP/259165/2019) Draft Guideline dated 29 May 2019
20 August 2019
IPAC-RS Rule20 MDR EU EC Letter Submission
bottom of page