AbOUT US

IDEAL Pharma Consulting is an independent contract research organization (CRO) providing research, analysis, and consultation services to pharmaceutical, biotechnology, generic, and medical device industries. We are specialised in the conduct, medical writing, study management and biometrics of clinical studies; especially Bioequivalence and Clinical Comparability Studies for Biosimilars.

With extensive experience in all areas of regulatory affairs, our teams coordinate, manage and support all aspects of clinical trials submissions to regulatory authorities and ethics committees. We also specialised inregulatory submissions/marketing authorisation applications and regulatory operational services, to the pharmaceutical and biotech industries.

IDEAL Pharma Consulting is located both in Istanbul and Ankara and with highly skilled and experienced staff organises Bioavailability and Bioequivalence (BA/BE) studies and efficacy / safety studies for similar biological medicinal products containing biotechnology-derived proteins as active substance in humans with the highest ethical, regulative and scientific standards.

IDEAL Pharma Consulting is committed to quality, cost and time effective customized service and the protection of the client's confidentiality.

IDEAL Pharma Consulting also pro­vides Phase I-IV clinical trial management services encompassing data management, PK/PD modeling, pharmacovigilance and regulatory consultancy.