Gruppen arbejder med erfaringsudveksling og vidensdeling indenfor kvalitetsstyring herunder fortolkning og implementering af regulatoriske krav, standarder og guidelines, på primære markeder, såsom EU og US. Desuden drøftes best practices indenfor forskellige områder herunder risikostyring, CAPA, leverandørstyring, audits, validering af processer og forberedelse til myndighedsinspektioner. Formålet er at styrke medlemmernes faglige kompetencer og understøtte høj kvalitet og compliance i medicoindustrien. Møderne afholdes typisk på engelsk.

The group focuses on knowledge sharing within quality management, including the interpretation and implementation of regulatory requirements, standards, and guidelines across key markets such as the EU and the US.
In addition, best practices are discussed across a range of areas, including risk management, CAPA, supplier management, audits, process validation, and preparation for regulatory inspections.
The purpose is to strengthen members’ professional competencies and support high levels of quality and regulatory compliance within the medical device industry. Meetings are typically conducted in English.