Mechanism of Coordinated Access to orphan medicinal products (MoCA)



MoCA takes its roots in the “Process on Corporate Responsibility in the Field of Pharmaceuticals” launched under the Belgian Presidency in September 2010, which was intended to identify areas for improved cooperation in the European Commission’s Communication on Industrial Policy due for publication in late 2012.

For further reference


Transparent Value Framework

The Process on Corporate Responsibility consisted of 3 pillars, the first of which was “Access to Medicines in Europe”. That pillar itself was sub-divided from the beginning into 6 different working groups, the second of which focused on the issue of “coordinated access to orphan medicinal products”. The formation of that working group marked the creation of MoCA.

In its original form, MoCA was intended to map innovative ways to provide real-life access to orphan medicines, in an affordable and sustainable way, for patients with unmet medical needs for whom these solutions would otherwise be out of reach. The main recommendation of the group was to develop a coordinated mechanism between volunteering Member States and orphan medicine developers to evaluate the value of an orphan medicinal product, which could be based on a transparent value framework, in order to support the exchange of information aimed at enabling informed decisions at Member State level on pricing and reimbursement. This, ultimately, should lead to more rational prices for payers, more predictable market conditions for industry and more equitable access for patients.

After the group completed their work in 2013, a few working group members decided to pursue discussions under the umbrella of the Medicines Evaluation Committee (MEDEV, an informal group of experts from statutory health insurance institutions and HTA agencies in Europe) with a view to putting all conclusions and recommendations into practice through the implementation of pilot projects focused on actual orphan medicines in development.

For further reference

MoCA Today

MoCA provides a mechanism for European countries to collaborate on coordinated access to orphan medicines in a voluntary, dialogue-based approach, intended to create a fluid set of interactions between key stakeholders, across all aspects of a product. The roles, responsibilities and prerogatives of each of the participating stakeholders should be respected.
It is important to stress that, to date, nowhere else in Europe does such a platform exist where companies’ issues around reimbursement or financing schemes can be discussed with such a variety of jurisdictions and societal perspectives.


Participation in MoCA is open to several stakeholder groups, including:

  • National competent authorities for pricing and reimbursement
  • Rare disease patients
  • Candidate marketing authorisation applicant/holders willing to be involved in a pilot focused on a particular product of theirs

Objectives of MoCA Pilots

Pilot projects retained within MoCA aim at facilitating “early dialogue” between companies and national competent authorities for pricing and reimbursement on specific orphan medicines, focusing discussions on a company’s strategy, the targeted disease, the product and its development, the approach and identified challenges to access markets with a view to ultimately helping to speed up access for patients in EU Member States to the product in question.

For further reference


Archive of Presentations about MoCA








Published Articles about MoCA




Other Documents with References to MoCA

For any question, please contact:

Anna Bucsics, MoCA Project Advisor
email: MoCA.OMP(at)

Maria Cavaller, Patient Engagement Junior Manager

Page created: 14/02/2017
Page last updated: 21/09/2020
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