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.
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
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