Trusted CRO Partner for Clinical and Bioanalytical Excellence
CSCRO approved CRO facility, successfully inspected multiple times by USFDA, EMA and having approval from ISP Chile regulatory. CRO Facility 160 bed clinical unit, GLP-compliant bioanalytical labs, and 150+ man-years of regulatory experience.
Our Accreditations
We are:
- Bioequivalence (BA/BE) studies
- Clinical trials (Phase I to IV) and PMS studies
- Bioanalytical services
- Regulatory & Medical Writing
- PK & Statistical Services
“Our commitment to quality, subject safety, and regulatory excellence sets us apart as a trusted partner in global drug development.”
4.4/5
107 Reviews
4.6/5
1630 Reviews
4.7/5
2100 Reviews
Why Choose Synergen Bio?
Global Regulatory Track Record
Successfully inspected by USFDA, EMA (BfArM & DKMA), CDSCO, and ISP Chile
State-of-the-Art Infrastructure
160-bed clinical facility, Phase I Unit, ICU, deep freezers, stability chambers and 11 LCMS/MS Systems
Experienced Multidisciplinary Team
150+ man years in each department of clinical operations, bioanalytical expertise & regulatory submissions for various markets.
Strategic Location
Located centrally in Pune, Maharashtra, India ensuring access to a large volunteer pool.
Partner with Synergen Bio for your next study and get one step ahead in your Drug Approval process
Address
101 to 105, 203, 205 to 207,
309 to 311, Sai Chambers,
302, Old Mumbai - Pune Highway,
Wakadewadi, Shivajinagar,
Pune, Maharashtra - 411003, India
Call Us
Email Us
info@synergenbio.com
