Example: barber
Annual Report 2016 - European Medicines Agency
Annual Repot 2016 4 5 Foreword & Introduction I am pleased to introduce EMA’s annual report for 2016 – my first year as Chair of EMA’s Management Board.
Tags:
Information
Domain:
Source:
Link to this page:
Documents from same domain
Guideline on good pharmacovigilance practices …
www.ema.europa.eu9 December 2013 . EMA/816292/2011 Rev 1* Guideline on good pharmacovigilance practices (GVP) Module VII – Periodic safety update report (Rev 1)
Q12 Step 2b Technical and regulatory …
www.ema.europa.euICH guideline Q12 on technical and regulatory considerations for pharmaceutical product lifecycle management EMA/CHMP/ICH/804273/2017 Page 3/36
Guideline on good pharmacovigilance practices (GVP)
www.ema.europa.euGuideline on good pharmacovigilance practices (GVP) – Module IX (Rev 1) EMA/827661/2011 Rev 1 Page 2/25
Guideline on good pharmacovigilance practices …
www.ema.europa.euGuideline on good pharmacovigilance practices (GVP) – Module VIII (Rev 3) EMA/813938/2011 Rev 3 Page 2/28
Guideline for good clinical practice E6(R2)
www.ema.europa.euGuideline for good clinical practice E6(R2) EMA/CHMP/ICH/135/1995 Page 2/70 Document History First Codification History Date New Codification
Guideline for good clinical practice E6(R2)
www.ema.europa.euGuideline for good clinical practice E6(R2) EMA/CHMP/ICH/135/1995 Page 2/75 10 Document History 11 First Codification History Date New Codification November
Guideline on good pharmacovigilance practices …
www.ema.europa.euharmful physical or psychological effects [DIR 2001/83/EC Art 1(1 6)]. 74 Adverse event (AE); synonym: Adverse experience 75 Any untoward medical occurrence in a patient or clinical- trial subject administered a medicinal product
European Medicines Agency
www.ema.europa.eu© EMEA 2006 2 SPECIFICATIONS: TEST PROCEDURES AND ACCEPTANCE CRITERIA FOR BIOTECHNOLOGICAL/BIOLOGICAL PRODUCTS ICH Harmonised Tripartite Guideline
products1/traditional herbal medicinal products
www.ema.europa.euThere is no expectation that existing herbal medicinal products on the market will be affected by this guideline, with the exception of traditional herbal medicinal products for human use that were already
Q7 Q&A - good manufacturing practice for active ...
www.ema.europa.euICH guideline Q7 on good manufacturing practice for active pharmaceutical ingredients – questions and answers EMA/CHMP/ICH/468930/2015 Page 2/37
Related documents
ANNUAL REPORT 2016 - NextEra Energy
www.nexteraenergy.comANNUAL REPORT 2016. Title: NEE-FPL 2016 10-K Created Date: 2/23/2017 11:00:00 AM
Annual Report 2016 - UKBMS
www.ukbms.orgUKBMS Annual Report 2016. The UKBMS. The UKBMS is run by Butterfly Conservation (BC), the Centre for . Ecology & Hydrology (CEH), and the British Trust for Ornithology
2016 ANNUAL REPORT - Tuan Sing
www.tuansing.comTA SIG HOLDIGS LIMITED 03 2016 Annual Report SUSTAINABILITY REPORT Sustainability at Tuan Sing 62 Investor Relations 64 Labour Practice & …