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ACT EU - Accelerating Clinical Trials · EU-wide · 27 Jun 2025 · Consultation

COMBINE Project 1: Call for expressions of interest in pilot all-in-one coordinated assessment

Original title: Call open for COMBINE Project 1: pilot “all-in-one” coordinated assessment

AI-generated summary

The European Commission, EMA, and participating Member States launched Phase 2 of the COMBINE Project 1 pilot on 26 June 2026 to test coordinated assessment of combined clinical trial and medical device applications across multiple Member States. Sponsors may submit a single application combining a medicinal product clinical trial with an in vitro diagnostic device study or medical device clinical investigation. Interested sponsors must complete an expression of interest form and protocol synopsis, submit them by the 23rd of the month before their intended submission month, and expect a decision by month-end. Phase 2 remains open for at least one year.

From ACT EU - Accelerating Clinical Trials

COMBINE Project 1 is exploring the coordinated assessment of combined study applications across:

- clinical trial and medical device regulatory frameworks

- multiple Member States.

This 'all-in-one' coordinated procedure is expected to:

- streamline the authorisation process

- reduce administrative burden for sponsors

- accelerate patient access to innovative treatments.

COMBINE project 1 pilot – Phase 2

The project proposes a phased pilot approach to test the feasibility of such a coordinated process. The pilot is designed to allow sponsors of combined studies to submit a single application for coordinated assessment.

The European Commission, participating Member States and the European Medicines Agency (EMA) are pleased to announce the launch of the second phase of the pilot on 26 June 2026.

This phase expands the scope of accepted applications and will extend the expression of interest period (this pilot phase will remain open for at least one year).

For this pilot phase, combined study applications should involve:

- a medicinal product clinical trial combined with

- an in vitro diagnostic medical device simultaneous performance study conducted by either the same eligible sponsor or separate sponsors, or

- a medical device clinical investigation conducted by either the same eligible sponsor or separate sponsors.

Resources

The Sponsor guide explains both eligibility criteria and the pilot process.

An overview of the key features of phase 2 is outlined in the Stakeholder Presentation from 28th May 2026.

Submission of an expression of interest

Sponsors interested in participating in the COMBINE project 1 pilot should:

- complete the expression of interest form

- prepare the synopsis of the proposed combined study

- create an EMA account and request access to Eudralink to EMA’s service desk. Once granted access to Eudralink, users will be able to create packages to include all the requested documents

- submit the expression of interest form and protocol synopsis to EUcombinepilotccmo [dot] nl (EUcombinepilot[at]ccmo[dot]nl, including Eudralink with the two documents (expression of interest form and protocol synopsis)

- if you already own an EMA account (usernameid [dot] ema [dot] europa [dot] eu (username[at]id[dot]ema[dot]europa[dot]eu)) you need to modify this using your professional or personal email address.

Please note:

- EUcombinepilotccmo [dot] nl (EUcombinepilot[at]ccmo[dot]nl mailbox is only for the expression of interest. Any other submissions or questions not related to this will be returned

- EUcombinepilotccmo [dot] nl (EUcombinepilot[at]ccmo[dot]nl mailbox will be closed after the period of expression of interest has ended

- the CCMO will ensure that the use of personal data complies with the rules and provisions set out in Regulation (EU) 2016/679. Further information is provided in the privacy statement within the expression of interest form

Excerpt from the official page. The original is authoritative. Continue reading at ACT EU - Accelerating Clinical Trials ↗