What we do

Portess Medical Writing Consultancy (PMW) offers professional medical writing services in tandem with strategic regulatory guidance and advice. Blending clear, accurate and concise scientific communication with insightful input to regulatory strategy, allows PMW to maximize the quality and efficiency of regulatory interactions across the drug development process.

Our team

Our team have a range of experience within the pharmaceutical company and writing agency environments, giving us a broad understanding of drug development and the pharmaceutical industry. We have extensive experience in preparing regulatory documents and a proven track record for delivering quality on time, while ensuring compliance with industry and regulatory guidelines. The PMW team have planned and delivered successful regulatory submissions across a range of markets (EU, US, Asia) and therapeutic areas.

Our clients

PMW has a proud history of delivering high quality regulatory documents and submissions, on time and within budget. We establish strong and durable collaborations so that PMW become an integrated and valued member of our clients' drug development teams. We adapt our ways of working to meet the specific needs of each individual client, allowing us to provide medical writing excellence for companies ranging from start-up biotechs to multinational pharmaceuticals, across Europe and the United States: