ELM Pharmaceutical Consultancy

We can take charge of coordination, advice of required studies, best centre search for technical and clinical development of generics or hybrids or for their well-established use for their future initial authorisation or during their life cycle, including:

Pharmaceutic studies: stability, dissolution, finished product specifications, biobatch production

Bioequivalence studies

Clinical studies

The Facilities and Centres chosen have recognised prestige and are well-accepted by European Agencies.