Insight Medical Writing

Danebrook Court
Oxford Office Village
United Kingdom

Phone: +44 (0) 1865 372 227

Skills and Services:

Insight MW is a specialist medical writing provider for the pharmaceutical industry. We offer medical writing services across the entire clinical research spectrum, including:

  • Common Technical Document (CTD)
  • Integrated safety and efficacy summaries (ISS/ISE)
  • Submission conversions and variations
  • Regulatory response to questions
  • Risk Management Plans (RMPs)
  • Clinical Study Reports (Phase I-IV)
  • Serious adverse event narratives
  • Periodic Safety Update Reports (PSURs)
  • Systematic Reviews
  • Protocols and amendments
  • Investigator brochures and updates
  • Manuscripts
  • Abstracts, slide and poster presentations
  • Medical marketing text


Our team of writers and consultants has written a wide variety of scientific and medical documentation, ranging from GLP reports to regulatory submissions and medical communications documents.

The long-standing relationship we have with many of our clients is evidence that they can depend on us to produce high-quality documents on time and within budget. Our writers have a thorough understanding of international regulations and guidelines and undergo continuous training with EMWA and other professional bodies. We have a wide range of research and clinical experience in multiple therapeutic areas, including:

  • Anti-infectives
  • Cardiovascular
  • Devices
  • Endocrinology
  • Gastroenterology
  • Haematology
  • Oncology
  • Orthopaedics
  • Respiratory
  • Rheumatology
  • Urology
  • Wound careĀ 

Other Information:

Insight MW understands the value of strong project management and a flexible working relationship with our clients. We:

  • Work independently yet collaboratively
  • Integrate with the project team
  • Produce the highest-quality documents with exceptional standards of clarity, accuracy, consistency and presentation
  • Write proactively to ensure that challenging timelines can be met
  • Anticipate potential problems through years of past experience with regulatory and publishing requirements