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Regulatory Services

With in-depth knowledge of local regulatory procedures and effective liaisoning with local regulatory agencies CEBIS ensures high efficiency in the Clinical Trial/BA-BE approval process.

Services offered are :

Executing regulatory submissions (Protocols, Ethics committee documents & compiling dossiers).

Preparation & submission of complete range of regulatory documents for obtaining:

  • Approval to conduct BA-BE studies/clinical trial in India.
  • Approval to import Test Drug.
  • Continuous follow-up post submission with regulatory authorities.
  • Renewal of Import license.
Copyright © 2024. CEBIS India Limited
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