Awaiting committee decision
2017/2710(DEA) Principles of and guidelines for good manufacturing practice for investigational medicinal products for human use and arrangements for inspections
Lead committee dossier: ENVI/8/10003
Role | Committee | Rapporteur | Shadows |
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Lead | ENVI |
Activites
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2017/05/31
Committee referral announced in Parliament, 1st reading/single reading
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2017/05/23
Initial period for examining delegated act 2 month(s)
- 2017/05/23 Non-legislative basic document published
Documents
- Non-legislative basic document published: C(2017)03368
History
(these mark the time of scraping, not the official date of the change)
2017-07-22Show (1) Changes | Timetravel
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2017-06-29Show (5) Changes
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