Basic info
Industry
pharmaceutical manufacturing
Sectors
eCTD
Medical Device
Internal Audits
Quality System Regulations
Qualified Person
Responsible Person
Price and Reimbursement
LiiV
GDP
Quality
MDR
EN ISO 13485
Pharmaceutical
GMP
Pharmaceutical Regualtory Affairs
Nordic Regulatory Office
Quality Training
QSR
Supplier Audits
Health Care
Medical Device Regualtory Affairs
FASS
Local PV officer
Translations
Date founded
1992