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Medical Writing Services for Clinical Trials :
Thinki ensures your clinical trial documentation is compliant with regulatory requirements, is concise, clear, concise, and scientifically and medically accurate. Medical writing services are available as an integral part of a full drug development program. Our medical writing team supports preparation of all regulatory documents, including:
  • Protocols
  • Investigator Brochures
  • Clinical statistical reports (ICSR)
  • CTAs
  • Marketing Applications
  • Scientific Reports
  • Patient safety narratives
What's New
CRQA is looking for
qualified and Independent
Pharmacvovigilance Auditor
- experience essential in
Pharmacovigilance Audits.
Interested Professionals
may apply to bd@crqa.in
CRQA is looking for
qualified and Independent
Pharmacvovigilance Auditor
- experience essential in
Pharmacovigilance Audits.
Interested Professionals
may apply to bd@crqa.in
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