This full service covers study design, protocol & Informed consent form(ICF) development, CRF design, Ethics committee review, Selection of subjects, bioassay of drug / metabolite, Pharmacokinetic and statistical data evaluations, reporting of study results, and archiving of all study related data.

Synchron has two separate state-of-the-art 30 bedded clinical units( total 60 beds) in the same premises and another 28 bedded clinical unit at different location in Ahmedabad. Each unit has adequate recreation facilities to conduct bio studies in healthy human volunteers, including women and post-menopausal women. We can conduct both male and female volunteer study simultaneously.

The BE & BA studies are carried out as per the appropriate SOPs.