We have extensive experience of working on clinical trials and bioequivalence
Studies submitted to US FDA, World Health Organization, Anvisa, Brazil, Health Canada, Drug Controller General of India and EMEA. Our services are strictly in compliance with ICH-GCP guidelines.
- Clinical Trial documentation
- Clinical Data Management
- Biostatistics in Clinical Trials
- Pharmacokinetic Analysis in BA/BE & Biostatistics in BA/BE
- Predictive Modeling