Whether your product is in the feasibility stage or you are ready to start a pivotal study to support your submission, at ProMedoss we provide a wide array of clinical trial services that will cover all your needs.

Our services include:

  • Project management

  • Investigator identification and recruitment

  • Study related binders/document preparation

  • Investigative site management and monitoring

  • Clinical supplies and CRF storage and shipment

  • Electronic Data Capture (EDC) Services

  • Investigator agreement and grant payment management

  • IRB management

  • Central laboratory management

  • Regulatory document/consent form approval and submission

  • AE/SAE reporting

  • Medical monitoring

  • Data Management

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