We are constantly amazed at the varied writing projects we are asked to support across diverse therapeutic areas. These include data-rich-research manuscripts, review articles, conference reports, film scripts, website material and patient consent forms in both English and German. We also author our own papers, including two recent pieces on Covid-19 and the pandemic (BMJ https://lnkd.in/dvYACJT; BJGP Life: https://lnkd.in/dXXziQT)
Clients keep coming back because we make complex information understandable. It is our ability to build relationships, appreciate your needs, and add a little extra magic.
Compliance with regulations, guidelines, and standard operating procedures ensures efficacy and patient safety. The ever-increasing demands of industry and regulatory bodies has led to a growing need for specialists who are able to deliver complex documentation and address challenging questions. Many in our team enjoy diving into the data and the structured approach required of regulatory writing.
Medical Device Writing
Devices are fun. Some 10-15 years ago, developers could bring their creations to the market with limited regulatory constraints. Collapsing hip implants and leaking breast prostheses have changed all this. Now the marketing requirements are approaching those required of most medicines. Hence the need for new and more detailed documentation. Further areas of complexity include in-vitro diagnostics, products which are both a device and a medicine, and the growing world of health Apps. Our digital division, Scividigital can help: