Medical Writing Services for Clinical Trials
Thinki ensures that your clinical trial documentation is compliant with regulatory requirements and is concise and clear along with being scientifically and medically accurate. Medical writingservices are available as an integral part of a complete drug development program. Our medical writing team supports preparation of all regulatory documents, including:
  • Protocols
  • Investigator Brochures
  • Clinical study reports (CSR)
  • CTAs
  • Marketing Applications
  • Scientific Reports
  • Patient safety narratives
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