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