Human medicines
Laboratory digitalisation: enhanced processes save resources
08.05.2024
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