Iris Bresink

With over 25 years of clinical development experience, including more than 20 years in medical writing and 5 years in regulatory affairs, Iris brings a wealth of knowledge and experience. Iris is an authorized pharmacist with a Ph.D. in pharmacology. Her medical writing experience includes developing and authoring clinical overviews, summaries of clinical efficacy and safety for NDAs/BLAs/MAAs, as well as life cycle management and various regulatory documents. She has extensive therapeutic experience across multiple areas. In recent years, Iris has played a key role in developing standards within the Medical Writing area of a larger pharmaceutical company and providing training for medical writers, particularly in strategic and regulatory writing. In 2024, Iris decided to start her own medical and regulatory writing business.