Generic Development Made Simple.
Our Expertise
– Integrated Clinical facilities suited for BE trials.
– High precision & standard compliance (GLP, ICH, local regulations).
– Volunteer recruitment capability tailored to study design.
– Timely reporting for regulatory submission.
Client Journey
1. Protocol Design
2. Volunteer Recruitment & Dosing
3. Sample Analysis & PK Evaluation
4. Final Report & Submission
Why Work with Us
– Local regulatory acceptance of BE studies.
– Access to well-controlled clinical environment, experienced staff, volunteer pools.
– Cost advantages vs. sending studies abroad.
– Large healthy volunteer pool causes speedy recruitment & study turnaround
Contact CTA
Book a BE study consultation.