RDG services of medical and regulatory writing are including:
- Product development plan
- CTD
- Pharmaceutical section of common technical documents (CTD)
- Normative document
- Regulatory applications
- Clinical development plan
- Protocols
- CRFs
- Investigator brochures
- Informed consent forms
- Clinical study reports
- Clinical sections of common technical documents (CTD)
- Abstracts, journal articles
- Periodic safety update reports (PSURs) and other pharmacovigilance documents
- Preclinical study report
- Medical and/or scientific literature review