Medical Writing
Combining clinical development experience with scientific rigour
With strong scientific backgrounds in a wide variety of therapeutic areas, and thorough knowledge of ICH GCP guidelines, and ISO standards, our Medical Writers are well-equipped to rapidly produce high quality, evidence-backed documents.
Our Medical Writers
The majority of our Medical Writers hold life sciences PhDs from leading Swedish and UK universities, and they have a cumulative 50+ years of clinical development and regulatory experience including:
First-in-human trials, Phase I – IV, post-marketing, Real-World Evidence (RWE), Medical Devices, Advanced Therapy Medicinal Products (ATMPs), and various scientific documents
Of course our other internal expert teams are always on hand as needed (e.g., Biostatisticians, Medical Experts, Medical Device Managers, RWE and Safety) to work in seamless collaboration. The Medical Writing team can support the whole product development life cycle – from scientific advice to protocol development, study reporting to post-marketing support.
