The clinical development plan (CDP) is a complex document that details clinical research strategy by describing scientific information and rationale of a drug, a list of clinical studies that will be carried out, an estimation of developmental costs, important deadlines, potential issues during development, regulatory and marketing strategies. A successful CDP provides the evidence of safety and efficacy required for regulatory approval.
The process of creating a high-quality CDP involves extensive collaboration and negotiation between experts from different fields. Our medical writers can help you to reach a consensus on CDP and together with our internal and external experts can ensure the scientific accuracy, quality and consistency of the document.