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Saturday, June 24, 2017
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Regulatory Affairs: The Mutual Recognition Procedure (MRP) (PRA21)

Certification Training Duration: 2 hours (the average time to complete the training program, including final assessments).
Credits Hours: 2
CPD Accredited TrainingAccreditation: This training course offers CPD accreditation from the Faculty of Pharmaceutical Medicine of the Royal Colleges of Physicians.
CPD Credits: 2
Demonstration: Demo an online course.

Certificate: View sample certificate.

PRICE: USD $195.00 LogoTraining Program: Regulatory Affairs: The Mutual Recognition Procedure (MRP)
Training Provided By:

Availability: Immediately available upon ordering.

Description: Online training with immediate access upon enrollment.

This online course discusses the special issues that are found when dealing with generic products in the Mutual Recognition Procedure (MRP). Facilitating agreements among participating states, the coordination group for Mutual Recognition and Decentralized Procedures also provides guidance to those states. This class explores the duration of the stages and sequence involved in the procedure, as well as the various players, timing and format of submissions, and requirements on content.

The Mutual Recognition Procedure is comparable to the Decentralized Procedure, except for the later involvement of the Concerned Member States in the assessment by the Reference Member State. A national license is converted to harmonized licenses given in various other member states which the applicant has chosen. The MRP (Mutual Recognition Procedure) is one of three routes offered to applicants in order to achieve multinational marketing authorization within the EEA (European Economic Area).

Once all course requirements have been satisfied, a certificate of completion is immediately available. Course takers can attempt the final assessment any number of times, as needed, in order to achieve a passing grade.

Benefits of Getting Certified at

By employing advanced e-learning training techniques, and coupling them with new automated tracking systems, the provides professionally designed online courses which are effective at training, and assist those interested with advancing their careers. The also assists companies through maintaining training records, the education of their employees, and assisting them with improving their overall quality of service.

Have Questions?

Should you have any particular question about this course, you can call us at (888) 111-1111 or send us an email at for more information.

Certification Requirements: Students must view the entire program and successfully pass an online, multiple-choice final assessment with >80% passing grade within a 90 day period of time (180 days for Professional Certification Programs). Certificate is accessible in PDF format immediately after satisfying requirements.

Online Training Programs Include:

  • Immediate access to training: Instructions, password, and username are emailed following order
  • 90 days of 24/7 access to individual training programs / 180 days for Professional Certification Program
  • Programs include voice-overs, easy navigation, progress checks, and high-quality animations
  • Course notes (in PDF) and/or references available with select training programs
  • Online final assessment with multiple-choice questions can be taken an unlimited number of times, until passing grade is achieved
  • A Certificate of Completion is immediately available once course requirements have been satisfied

The Regulatory Affairs: The Mutual Recognition Procedure (MRP) Course is Found in the Following Professional Certification Program(s):

International Regulatory Affairs Professional Certification Program: This professional certification program includes descriptions of the decentralized procedure (DCP), EU variations procedure, the mutual recognition procedure (MRP), the European centralized procedure (CP); requ … Learn more


This session provides background information. It covers products for which the MRP can be used, the types of Marketing Authorisation Application, and characteristics of the application procedure.

The MRP process
This session takes you through the entire process from initial national authorisation by the RMS to the issuing of national licences by the CMSs. Referral of issues to the CMD, and the arbitration process, are also covered.

Generics and the MRP
This session gives a brief introduction to generics and the special issues that apply to generic products in the MRP.


Students completing this course should be able to:

–Provide an overview of the MRP 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.


313 Regulatory jobs found.
Displaying jobs #1-4.

Regulatory Reporting Specialist
Posted Date: 2017-06-23
COOK MEDICAL – United States, IN, Bloomington, 47404

Clinical Research Regulatory Affairs Manager
Posted Date: 2017-06-19
Medix – United States, WA, Seattle, 98127

Regulatory Compliance Analyst
Posted Date: 2017-06-19
Apex Life Sciences – United States, MD, Rockville, 20849

Associate Director Regulatory Affairs CMC
Posted Date: 2017-06-21
Ascent Life Sciences – United States, MA, Waltham, 02254

See more Regulatory Jobs

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