SUB11

The Decentralised Procedure (DCP)

The DCP is one of three routes available to applicants to gain multinational marketing authorisation within the European Economic Area (EEA) on the basis of a single application. It can be used only for a product which has no existing marketing authorisation in any member state. It is similar to the Mutual Recognition Procedure (MRP) but with earlier involvement of the Concerned Member States in the assessment by the Reference Member State. The Coordination Group for Mutual Recognition and Decentralised Procedures (CMD) provides guidance and acts to facilitate agreement among the participating states.

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.

Approximate Course Time: 2 hours

Level: Intermediate

CPD Points: 2

Audience: Regulatory

Category: Regulatory Submissions

Region: Europe

Who will benefit from this module?

This module is primarily aimed at regulatory affairs professionals dealing with marketing authorisation applications and related submissions for regulatory approval in Europe. More generally, it will also be of interest to all those involved in the development and registration of medicinal products.

Learning objectives

  • 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.

Module outline

Module overview – 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.

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.

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.

Assessment – Multiple-choice mastery assessment.

About Zenosis

Benefits of Zenosis

Essentials

Regulatory Affairs & Compliance

Clinical Trials

Good Manufacturing Practice

Drug Safety and Pharmacovigilance

Pharmacokinetics and Pharmacodynamics

Information and Communication Technology

Buy Online Course(s)

Terms & Conditions

Download Zenosis Catalogue