Insight Medical Writing

Address:
Email: info@insightmw.com
Website: http://www.insightmw.com/
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

Expertise:

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 care 

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