Clinical Trial Monitoring Services In India | Biomedra
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Clinical Trial Monitoring

The Medical & Safety Monitoring staff, Physicians (MDs) at our facilities have extensive experience. They see to it whether the to-be undertaken research has protocol eligibility and also ensure compliance to safety reporting guidelines set nationally and internationally. With all this, premium quality precision is assured in projects from almost every therapeutic domain.

  • Providing services related to development of clinical plans
  • Providing input for protocol design
  • Advising protocol team on monitoring safety
  • Ensuring timely communications to sponsors and concerned authorities
  • Preparing SAE narratives for the purpose of regulatory reporting
  • Evaluating untoward events/ SAEs
  • Reviewing safety reports prepared
  • Reviewing in medical terms all study team deliverables

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