The "Development of Combination Products: Critical Interactions Training Course (Feb 9th - Feb 10th, 2026)" training has been added to ResearchAndMarkets.com's offering.

The programme will cover the regulatory strategy to adopt and the relevant aspects of GMP and quality processes, including the data expectations for the CTD. It will also review the key relationships between quality, regulatory, R&D and production. Delegates will find this a comprehensive overview of the requirements for these products and will have an opportunity to discuss the complexities with an expert in this field.

Drug/device and device/drug combination products are becoming increasingly important in the medical industry. The development and manufacture of these products raises a number of complex issues and the quality and regulatory aspects are challenging. This interactive seminar will clarify the EU and US approach to drug/device and device/drug combination products, address the requirements for the device technical file/design file, explain the biological and synthetic drug regulations and look at the registration procedures for these products.

Benefits of attending:

• Clarify the definitions for drug/device and device/drug combination products in the EU and USA
• Consider the requirements for the device technical file/design file
• Comply with the biological and synthetic drug regulations
• Understand the registration procedures for devices and medicines in the EU and USA
• Determine the data required for the Common Technical Document (CTD)
• Consider the regulatory strategy depending on your product
• Gain practical advice on how to apply the ISO standards

Who Should Attend:

• All development, regulatory and quality personnel involved in the development of combination products (drug/device and device/drug products)
• Pharmacovigilance/vigilance personnel
• Device experts looking to expand their knowledge to medicines and vice-versa

Certifications:

• CPD: 12 hours for your records
• Certificate of completion

Key Topics Covered:

Day 1

Defining a drug/device and device/drug product

• EU approach
• US approach

Regulatory procedures for drug/device and device/drug products

• EU procedures
• US and Office of Combination Products

Understanding devices

• Medical Device Regulation - EU
• CE marking and Notified Body interactions
• CDRH definitions - US - 510(k) and PMA
• Labelling
• Vigilance requirements

Device technical file/design file

• What is required
• Structure
• Bench testing
• Potential clinical requirements

Workshop: Technical file/design file

Understanding the biological and synthetic drug regulations

• EU/US definition of medicinal product
• Labelling
• Pharmacovigilance
• Quality requirements

Day 2

Registration procedures

• EU approach
• US approach

GMP and ISO standards

• Practical application
• Interpretation of the standards

The CTD

• Where to put data
• Data expectations
• Applying QbD (quality by design)

Workshop: CTD requirements - tracking critical documents

Key considerations for the regulatory strategy

• Deciding which regulatory route to take
• Device and product registrations
• Combination-only registrations
• Desired labelling

Workshop: regulatory strategy

For more information about this training visit https://www.researchandmarkets.com/r/mquu9m

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