- Highest quality clinical services as per ethical norms.
- Successful bio-analytical method development and validation of even industry-challenging molecules.
- Finalizing the protocol and report as per the sponsor's specific requirements.
- Professional data management through validated processes and reporting services.
- Pharmacokinetic studies - Multiple dose studies - Food effect studies - Steady-state studies
- Clinical facility includes spacious subject housing units, segregated counseling and screening areas, closely monitored and frequently audited kitchen with approved meal plans from dietician.
- Bioavailability / Bioequivalence Studies carried out for of all therapeutic categories & classes of subjects, using in house SOPs developed as per ICH-GCP Guidelines, ICH E3 guideline.
SCR have capability to undertake number of clinical trials in different therapeutic area which had been started with other CROs/Sponsors elsewhere but did not meet out the expectations/targets.
- Experienced and large Investigator data which have good patient pool to speed up recruitment
- Site Coordinate by SCR staff who respond timely
- Fast set up of rescue model