We perform our activities on the basis of our own Standard Operating Procedure (SOP) or that provided by our Client, as requested.

• Creating, releasing and checking SOPs
• Trial Document Management
• Communication with Sponsor / Contracts
• Authorisation of clinical studies /
  Communication with HA and CEC
• Selecting Sites for Clinical Studies
• Conducting Initiation visit / Site Training
• Conducting Routine monitoring visit
• Conducting close-out visit
• Handling of Case Report Form (CRF)
• Maintaining the Investigator Brochure (IB)
• Handling of Investigator Site File
• Handling and reporting Serious Adverse Events (SAE) in Clinical Trials