See below for some great resources about medical writing and clinical trial transparency!
DIA Global
DIA fosters innovation to improve health and well-being worldwide. DIA is a global association that mobilizes life science professionals from across all areas of expertise to engage with patients, peers, and thought leaders in a neutral environment on the issues of today and the possibilities for tomorrow.
The Regulatory Affairs Professionals Society (RAPS) is the largest global organization of professionals involved with regulatory and quality for healthcare products, including medical devices, pharmaceuticals and biologics, diagnostics, and digital health.
The Society of Clinical Research Associates (SOCRA) is a non-profit, charitable and educational membership organization committed to providing education, certification, and networking opportunities to all persons involved in clinical research activities.
EMWA is the European Medical Writers Association. EMWA is the network of professionals that represents, supports and trains medical communicators in Europe and beyond.
ClinicalTrials.gov is a website and online database of clinical research studies and information about their results. The purpose of ClinicalTrials.gov is to provide information about clinical research studies to the public, researchers, and health care professionals.
European Medicines Agency Clinical Trials Regulation
The European Union (EU) Clinical Trials Regulation (CTR) aims to ensure the EU offers an attractive and favorable environment for carrying out clinical research on a large scale, with high standards of public transparency and safety for clinical trial participants.
Health Canada Public Release of Clinical Information
Health Canada PRCI aims to make anonymized clinical trial information for approved drug and medical device applications accessible to the public and scientific community.
See below for some great resources about medical writing and clinical trial transparency!