Communication from the Ministry of Health No 308 / 2021 Coll.
Communication from the Ministry of Health on the publication of Commission Decision (EU) 2021 / 1240 of 13 July 2021 on the compliance of the EU portal and the EU database for clinical trials of medicinal products for human use with the requirements referred to in Article 82 (2) of Regulation (EU) No 536 / 2014 of the European Parliament and of the Council
Valid
Communication
Text versions:
25.08.2021
308
COMMUNICATION
Ministry of Health
of 13 August 2021
on the publication of Commission Decision (EU) 2021 / 1240 of 13 July 2021 on the compliance of the EU portal and the EU database for clinical trials of medicinal products for human use with the requirements referred to in Article 82 (2) of Regulation (EU) No 536 / 2014 of the European Parliament and of the Council
The Ministry of Health shall communicate on the basis of Article VIII (a) and (b) of Act No. 66 / 2017 Coll., amending Act No. 378 / 2007 Coll., on Medicines and on Amendments to Certain Related Laws (Act on Medicinal Products), as amended, and on the basis of Article III of Act No. 44 / 2019 Coll., amending Act No. 378 / 2007 Coll., on Medicines and on Amendments to Certain Related Laws (Act on Medicinal Products), as amended, and Act No. 372 / 2011 Coll., on the Compliance of the EU Portal and the EU Database for the Clinical Evaluation of Human Medicinal Products with the Requirements referred to in Article 82 (2) of Regulation (EU) of the European Parliament and of the Council (EU Official Journal of the Official Journal of the European Union), which provides that the portal and the amended Commission Decision (EU) 2021 / 1240 of 13 July 2021 on the compliance of the EU portal and the EU database on the EU database.
Minister for Health:
Mgr. et Mgr. Vojtěch, MHA, v. r.
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Regulation Information
| Citation | Communication from the Ministry of Health No 308 / 2021 Coll., on the publication of Commission Decision (EU) 2021 / 1240 of 13 July 2021 on the compliance of the EU portal and the EU database for clinical trials of medicinal products for human use with the requirements referred to in Article 82 (2) of Regulation (EU) No 536 / 2014 of the European Parliament and of the Council |
|---|---|
| Regulation Type | Communication |
| Author | - |
| Collection | Code of Laws |
| Date of Promulgation | 25.08.2021 |
|---|---|
| Effective from | - |
| Effective until | - |
| Status | Valid |
Legal Areas:
Administrative law
Health
The regulation text is for informational purposes only.
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