We can plan, organise and carry out clinical studies (phases I to IV) as well as bioavailability and bioequivalence studies for all pharmaceutical forms.

• Drafting of clinical study records in accordance with individual customer requirements
• Approval of clinical study protocols by independent ethics committee


• Approval of study protocols by the committee for medicinal products of the State Institute for Drug Control (SIDC)


• Clinical trials insurance in accordance with Slovakian law


• Clinical studies, bioavailability studies and bioequivalence studies carried out on healthy subjects at the company own clinic and research facilities


• Clinical studies organised and carried out in conjunction with partner clinics and hospitals


• Monitoring of clinical studies


• Statistical evaluation of study results


• Drafting of final study reports

If you require more information please consult the following contact.

If you do already have a concrete enquiry, please fill out this form. You can directly send it to us: Checklist for Bioequivalence Study