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Key Facts

Czech Republic

Map of Czech Republic

Reception Date

02.10.19

Category

PHARMACEUTICAL AND COSMETICS

Pharmaceuticals

Ministries & Departments

Ministerstvo zdravotnictví České republiky, odbor legislativní

Responsible Departments

Úřad pro technickou normalizaci, metrologii a státní zkušebnictví

Products & Services concerned

Medicinal products for human use according to the definition under Directive 2001/83/EC of the European Parliament and of the Council of 6 November 2001 on the Community code relating to medicinal products for human use

Related EU Law

-

Explanation

The previous amendment supplemented the Act with measures against undesirable distribution outside the Czech market of medicinal products intended for Czech patients.

Summary

The purpose of the draft Act is to contribute to better availability of pharmaceuticals to Czech patients through a combination of interrelated measures:

Notification Timeline

This timeline summarizes key events in the notification process

Law is drafted in Czech Republic Czech Republic notifies the draft law 02.10.19 Draft law returns to Czech Republic Commenting Periode Ends 03.01.20 1 Member States & EC Responses 0 Detailed Opinions 1 Comments 1 External Stakeholders Responses

Notification Comparison

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Commenting Organisations

This section lists all organisations that have submitted comments on this notification. Each entry includes the organisation’s name, the number of contributions made, and a link to view their comments. Explore the list to understand which stakeholders are actively engaging in the consultation process.
Organisation Comments Date Total Contributions
EAEPC - European Association of Euro-Pharmaceutical Companies Not published 2019-11-28 2
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See for example the Network of CEMBUREU (Affiliation & Member Organisations)