Řízení v oblasti veřejného zdraví EU

Improving health systems

Výchova k péči o zdraví

Medical devices

Substances of human origin

Krev, tkáně a orgány

Léčivé přípravky

Ochrana před nemocemi

Posuzování rizik

Vědecké výbory

Endocrine disruptors

Endocrine disruptors

Biocides

Biocides

Konzultace

Closed consultations

16 Listopad 2015 - 15 Únor 2016

Public consultation on notice from the Commission on aspects of the application of Article 3, 5 and 7 of Regulation (EC) N° 141/2000 on orphan medicinal products
15 Září - 11 Prosinec 2015

Public consultation on EU GMP Guidelines, revised Annex 17 on the Real Time Release testing
28 Srpen - 24 Listopad 2015

Public consultation of the Commission guidelines on good manufacturing practice for investigational medicinal products
28 Srpen - 24 Listopad 2015

Public consultation on detailed arrangements for clinical trial inspection procedures including the qualification and training requirements for inspectors pursuant to Article 78(7) of Regulation (EU) No 536/2014
28 Srpen - 24 Listopad 2015

Public consultation on Good Manufacturing Practice for Medicinal Products for Human Use
28 Srpen - 24 Listopad 2015

Public consultation on the Commission Delegated Act on principles and guidelines on good manufacturing practice for Investigational Medicinal Products and on inspection procedures
23 Červenec - 12 Listopad 2015

Targeted stakeholder consultation on the development of Guidelines on Good Manufacturing Practice for Advanced Therapy Medicinal Products pursuant to Article 5 of Regulation 1394/2007
14 - 31 Květen 2014

Public consultation on the application of Regulation on Maximum Residue Limits (MRLs)

Public consultation on the application of Regulation on Maximum Residue Limits (MRLs)
06 Únor - 31 Květen 2014

Public consultation on the revision of Annex 15: Qualification and Validation
09 Říjen 2013 - 03 Leden 2014

Public consultation on the Commission guideline on paediatric investigation plans

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