Human medicines
Compliance review of promotional materials related to medicines, medical devices, food supplements and cosmetics in the Baltic countries
18.04.2024
Pharmaceutical-technological expertise ensuring successful drug development projects and manufacturing of IMPs
17.04.2024
Tenboron & Medfiles: working together in cancer drug development
15.04.2024
Free guide: Quick tips for successful CTIS submissions
04.04.2024
A team of 14 experts ensures high-quality regulatory and pharmacovigilance services in the Baltic countries
18.03.2024
Planning an investigator-initiated study (IIS)? 10 tips for a successful outcome
11.03.2024
Global pharma company & Medfiles: cooperation in obtaining and maintaining marketing authorisations in the EU
08.03.2024
Six reasons to engage regulatory CMC experts in drug development at an early stage
20.02.2024
Marketing authorisation application processes efficiently under one roof – for all EU countries
12.02.2024