Medical Writing

  • Writing of critical documents for medicinal products
    • Module 1.6 (environmental risk assessment)
    • Module 1.8 (pharmacovigilance)
    • Module 2.4 (nonclinical overview)
    • Module 2.5 (clinical overview)
    • Module 2.6 (nonclinical summary)
    • Module 2.7 (clinical summary)
    • Addendum to Clinical/Nonclinical Overview (renewal)
  • Team of experts with wide experience from the pharmaceutical industry, as scientists, as drug safety experts and as clinicians