|
Fred O. Smith, MD offers a unique combination of medical practice and pharmaceutical experience, to assist PharmSupport’s pharmaceutical and biotechnology clients with clinical and medical issues in drug development. PharmSupport offers:
- Medical review of documents (e.g., regulatory submissions, clinical study reports, subject narratives)
- Assistance with clinical development plans and strategy, from a medical and scientific perspective
- Medical review of adverse event coding (e.g., in MedDRA)
- Drug safety support and review
- Assistance with clinical study design and clinical study protocol writing
- Medical support for clinical study investigators and for investigator-initiated clinical trials
Please contact PharmSupport to discuss how we can help you!
|
|
