Postmarketing experience reports


• Our writers at ClinScript are involved from the early stages (e.g. preparing clinical development plans, IMPDs or INDs) of clinical Development, means that thoughts and messages are clearly structured and presented from the beginning, which streamlines the writing of all later documents.

• Utilizing a ClinScript dedicated team to prepare not only the main regulatory documents, but also supportive regulatory documents (e.g. subject narratives, Informed Consent Forms, Risk Management Plans, Periodic Safety Update Reviews,) and documents based on information originating from regulatory documents (e.g. manuscripts, posters) ensures consistency and continuity – making the overall writing process more efficient.

• All documents benefit from having been prepared by a professional writer.