For successful protocol writing, begin with the purpose and keep in mind who ultimately will be using this document.| blog.amwa.org
Medical communicators who work in the pharmaceutical space will recognize some features of medical device writing. Regulatory writers for drugs and devices are a part of the effort to bring safe, effective medical products to the public. Therefore, writers in both specialties need to be familiar with a field that is changing as fast as the technology itself.| AMWA Blog
An exploration of the similarities and differences between regulatory medical writing and regulatory affairs professions.| blog.amwa.org
AMWA’s Measures of Success Toolkit delves into the details of quality, timelines, and stakeholder involvement, providing expert insights on this critical medical writing specialty.| blog.amwa.org
A brief guide to evolving guidance and regulations on the use of artificial intelligence in the pharmaceutical industry.| blog.amwa.org
Medical communicators can help ensure that clinical trials adhere to guidelines and principles that support diversity, equity, and inclusion (DEI) in research and applying inclusive language principles in health communication.| blog.amwa.org