Profile:
India focused CRO with 19 years experience of managing Phase I to IV studies for global blue-chip as well as emerging pharma & biotech companies based at US, EU, Japan & Australia. Unique operational systems make us Underwrite Compliance with regulations, time-lines & budget. Best regulatory interface in India. Availed by world's biggest Biotech conglomerate.

Categories

Case Report Forms

Clinical Pharmacology

Clinical Trial Design

Clinical Trial Monitoring

GCP Compliance

Patient Recruitment

Project Management

Regulatory Affairs/Regulatory Strategy

Regulatory Document Preparation

Trial Management