This module describes the roles of the various players in the procedure, the sequence and duration of the stages involved, and the requirements on content, format and timing of submissions. It discusses the special issues that apply to generic products in the DCP.
- Provide an overview of the DCP process.
- Describe the pre-submission and submission actions in relation to timeline deadlines.
- Specify the responsibilities of the Reference Member State (RMS), the Concerned Member States (CMSs) and the applicant.
Provides an overview of the content of the module and outlines related Zenosis modules.
An introduction to the Decentralised Procedure
This session provides background information. It covers products for which the DCP can be used, the types of Marketing Authorisation Application, and characteristics of the application procedure.
The DCP Step 1
This session takes you through the pre-procedural step and the first assessment stage of the DCP, as far as day 120.
The DCP Step 2
This session takes you through the second assessment stage and the final step of issuing national licences. Referral of issues to the CMD, and the arbitration process, are also covered.
Generics and the DCP
This session gives a brief introduction to generics and the special issues facing generics in the DCP.
Multiple-choice mastery assessment.