Pharmaceutical Information Division
- Assesses the compliance of medicinal product quality documentation with the requirements of normative acts.
- Assesses the compliance of the bioanalytical section of bioequivalence studies with the requirements of normative acts.
- Prepares information regarding quality of medicinal products for communication with doctors, pharmacists and the public.
- Assesses the compliance of medicinal product labelling with the requirements of normative acts.
- Ensures the conduct of the Baltic labelling procedure.
