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Medical Writing

Our writers have diverse therapeutic backgrounds with experience in the preparation of a wide range of scientific materials. 

To ensure that the expectations and needs of the intended reader are taken into account, it helps to start with the question, ‘For whom is this document being written?’ Domain expertise, knowledge of the target audience and effective communication of findings and conclusions are critical skills for a writer of medical documents at PPCE.   


Our panel of medical writing experts will ensure that scientific and medical documents entrusted to us are crisp, clear and fully compliant with regulations and best practices.


  • Phase I-IV Protocols

  • Registry Protocols

  • Phase I-IV Clinical Study Reports

  • Manuscripts & Articles for Journals

  • Informed Consent Forms

  • Investigator Brochures

  • Patient Safety Narratives

  • Common Technical Documents

  • Periodic Safety Update Reports


  • Regulatory compliance: Development of well, structured, clear documents that follow ICH-GCP and other applicable guidelines.

  • Customer confidence: In-house Quality Control and Due Diligence processes ensure technical and grammatical precision.

  • Timeliness: High quality output and on-time delivery - no excuses!

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