MEDICAL AFFAIRS AND REGULATORY SCIENCE

Research results, product use, and other medical information should be clearly and concisely written and this well-structured documentation plays a major role, especially in the approval process for drugs, devices and biologics. Symyoo’s medical affairs and regulatory science (MA & RA) team is comprised of medical experts with unparalleled project experience related to marketing authorization procedures and clinical trial applications in addition to common technical document (CTD) writing. Symyoo’s MA & RS team has also full competence in medical affairs covering activities of advice and support with drug development and study start-up consultation.

    Services

  • Consultation on Drug Development
  • Common Technical Document (CTD) Writing
  • Investigational New Drug (IND) Application