Whatever your medical writing needs, Clinserv has the right team to deliver the quality and timeliness to ensure your projects’ success.

You can count on our medical writers at any point in your product development lifecycle, from the Clinical Development Plan to individual Clinical Study Protocols, Reports and Manuscripts, ultimately to the Regulatory Submission Documents (including eCTDs) to different regulatory authorities (EMEA, AFSSAPS, FDA).

We can also help with Safety Reports, Patient Narratives or any other type of document involving study data.
With a full complement of medical writing services, Clinserv has all you need in all your documentation and writing projects.

All our medical writing services are compatible with ICH guidelines and other regulatory requirements, not to forget our High Level of internal quality control for our writing projects.
 
  Project Management

  Study Monitoring

  Medical Writing

  Medical Devices

  Regulatory Affairs

  Site Management

  Training and Development

  Data Management & Statistics

  Biological and IMP Logistics

  Quality Assurance