IDE® Pharmaceutical Consultancy

We were established in 1998 as a ‘’ Contract Service Organization (CSO)’’ providing completely integrated services. Today, we are a well know Contract Service Organization (CSO) in Turkey, being the first in our field, with the qualification based on our 20 years of experience in Bioequivalance, Marketing Authorization and Biopharmaceuricals, in providing extensive scientific and training services in strict adherence to internationally recognized guidelines and regulations, fully respecting confidentiality. Our Services; Compassionate use procedures Acting as ‘applicant’ and ‘holder’ for marketing authorization Marketing authorization services GMP application and support Expert report preparation Scientific consultancy and training Formulation development consultancy Procuring reference/comparator drugs for R%D and bioequivalance studies Procuring internationally controlled reference/comparator drugs for R&D and bioequivalnce studied Dissolution investigations Bioequivalance and therapeutic equivalance investigations Therapeutic equivalance for pharmaceutical and biosimilar products Biowaiver dossier preparation Reimbursement dossier preparation Other- Preparing price application files Pharmaceutical assessment studied and legal and regulatory advice Expert assistance for establishing a company in Turkey Risk management.