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What We Do 

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We'll provide your site with

  • Highly trained staff qualified staff with a surplus of industry experience.

  • Regulatory document completion per FDA /GCP guidelines.

  • ICH-GCP and IATA training.

  • Handling of the Feasibility and Study Start-up process.

  • Identifying studies that fit your site’s patient population.

  • Patient and Investigator Invoicing.

  • IRB Submissions, Maintenance, and Renewals.

  • SOP Creation and Maintenance.  

Medical Team

We'll Also..

  • Act as Communication Liaison between the Clinical Site and the Pharmaceutical Companies.

  • Provide Study coordinators, Data coordinators,  Regulatory coordinators, and Budget and Contract Specialist .

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