Daily overview

Selection from Decision-Making Practice - 8/2026

Pharmeca a.s. 28. 04. 2026

The Ministry of Health (MoH) assessed whether the maximum price of the so-called “first similar medicinal product” may be increased after an abbreviated reimbursement review, or only after an abbreviated review of maximum prices. The key issue in dispute was therefore the interpretation of the term “the first subsequent abbreviated review”, which is set out in the Public Health Insurance Act as a condition for a potential increase in the maximum price.

In the proceedings, the State Institute for Drug Control (the Institute) argued that this must refer exclusively to a review of maximum prices. As only a reimbursement review—and not a price review—had been conducted in the relevant group, the Institute rejected the application as inadmissible.
The appellant, by contrast, argued that the Act does not distinguish between a price review and a reimbursement review.

In its decision, the MoH stated that the Act refers generally to “an abbreviated review under Section 39p”, which covers both price reviews and reimbursement reviews. In its view, the Institute’s interpretation was overly restrictive.
The original purpose of the reduction in price and reimbursement for the first generic was to prevent high patient co-payments upon its market entry. Once the Institute had carried out an abbreviated reimbursement review, reimbursement levels were aligned across all products within the relevant group, thereby eliminating the risk of inequality in patient co-payments.

For these reasons, the MoH concluded that the completion of an abbreviated reimbursement review is sufficient to allow the submission of an application for a price increase and, on that basis, annulled the Institute’s decision by which the proceedings had been discontinued.



Are you interested in reading regular commentaries on decisions by Pharmeca a.s.? Feel free to contact us.

At Pharmeca, we help you navigate the complex landscape of pharmaceutical and medical device information. We also offer flexible services that can be tailored to your needs at any time.

Our market position and experience allow us to support you whenever you need expert guidance.

Our knowledge, your opportunity.

 

Articles on decision-making practice are based on publicly available texts from the decisions of the Ministry of Health of the Czech Republic and the State Institute for Drug Control (SÚKL).

A continuously updated overview of decisions issued by SÚKL and the Ministry of Health in the field of pricing and reimbursement is available on the Pharmeca a.s. website.

The text was translated using ChatGPT 5.3. 

Back to news listing