A Practical Guide To Writing Risk Management Plans (Rmps) 1-Day Online Training Course (Nov 12Th, 2025) With 6 CPD Hours Learn To Navigate ICH And EU RMP Guidelines Effectively

(MENAFN- GlobeNewsWire - Nasdaq) Opportunities arise from providing training on EU RMPs, emphasizing compliance, updates, and efficient use of templates. Attendees gain insights into regulatory processes and the relationship between RMPs and safety studies, plus certification benefits, positioning the service as crucial for regulatory success.

Dublin, Sept. 23, 2025 (GLOBE NEWSWIRE) -- The "A Practical Guide to Writing Risk Management Plans (RMPs) Training Course (Nov 12th, 2025)" has been added to ResearchAndMarkets's offering.

In the EU, all companies are required to provide risk management plans (RMPs) for every new product, whether generic products or new chemical entities, and these RMPs must also be modified and updated throughout the lifetime of a medicine.

This intensive one-day course will provide you with an invaluable overview of writing and maintaining RMPs, with practical advice to ensure you achieve regulatory compliance. You will discuss best practice for using the EU templates and risk minimisation tools to enhance the benefit/risk of your product.

The programme has been fully revised to cover the latest updates and new requirements, including amendments made to the previous template.

Benefits of attending:

• Gain an overview of ICH and EU RMPs - their production and ongoing maintenance
• Clarify the documentation to be supplied to regulators and the process for RMPs
• Learn what happened in the EU RMP update and explore the new requirements
• Discuss the EU templates and their completion - generic and innovative products
• Understand the relationship between RMPs, post-authorisation safety and efficacy studies, safety reviews and PBRERs
• Discuss the RMP and risk minimisation follow-up

Certification:

• CPD: 6 hours for your records
• Certificate of completion

Who Should Attend?

This course will be relevant for those working in pharmacovigilance who are involved with writing RMPs, including medical directors/QPPVs who approve such plans. It will also be of interest to those who work with pharmacovigilance, e.g. in regulatory affairs, clinical, pre-clinical, sales and marketing, legal, commercial and quality.

Key Topics Covered

Introduction, welcome and objectives

An introduction to RMPs

• Outline and purpose of ICH E2E
• The implementation of ICH E2E
• National adoption of ICH E2E
  • Europe
  • USA
  • Japan
  • Arab States

Outline of EU RMPs

• The current EU module V requirements
• Generic, innovator and advanced therapy products
• Additional documents to supply to the regulators
• Safety reporting timelines for RMPs
• EU RMP update and new requirements

The EU templates and their completion - generic and innovator products

• The EU generic template - EU requirements (module V)
• The EU generic RMP versus innovator RMP
• The EU template for innovator products

Completion of RMPs in other countries

The EU RMP and relationship with other documents

• The RMP post-authorisation safety and efficacy studies
• The RMP and PBRERs
• The RMP and safety reviews

The RMP and Risk Minimisation Follow up

Overview of the sections of the EU RMP template

• Part I - Product overview
• Part II - Safety specification modules SI-SVIII
• Part III - Pharmacovigilance plan including safety studies
• Part IV - Plans for post-authorisation efficacy studies
• Part V - Risk minimisation activities including effectiveness measures
• Part VI - Summary of the risk management plan
• Part VII - Annexes

Final discussion session

For more information about this training visit

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