Phase I -
IIa & Bioavailability and Bioequivalence Studies
We conduct
FASTING STUDIES
FOOD EFFECT STUDIES
INTERACTION STUDIES
MULTIPLE DOSE AND STEADY STATE STUDIES
LINEARITY STUDIES
INVITRO-INVIVO CORRELATION
PK-PD MODELING
DERMATOPHARMACOKINETICS
This full service covers study design, protocol writing, 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 28 bedded clinical units(
total 56 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. Click on the photo gallery images
below for its full view.
The BE & BA studies are carried out with the help of detailed
SOPs.
Phase I-IIa BA/BE
FASTING STUDIES