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Pharmacovigilance
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#	Item
51	CMD(h) meeting with interested parties Add to Reading List Source URL: www.hma.eu Language: English - Date: 2015-05-29 10:17:02 Clinical research Pharmaceuticals policy Drug safety Healthcare quality Clinical data management Electronic common technical document Pharmacovigilance
52	QuarterWatch Monitoring FDA MedWatch Reports Why Reports of Serious Adverse Drug Events Continue to Grow October 3, 2012 Data from 2012 Quarter 1 Add to Reading List Source URL: www.ismp.org Language: English - Date: 2012-10-03 12:53:27 Food and Drug Administration Clinical research Thiophenes Healthcare quality Medical terminology Adverse Event Reporting System Duloxetine Pharmacovigilance Rivaroxaban Adverse effect Adverse event MedWatch
53	DOC Document Add to Reading List Source URL: www.ema.europa.eu Language: English - Date: 2016-07-20 07:22:57 Clinical research Pharmaceutical industry Clinical data management Drug safety Electronic common technical document Supplementary protection certificate European Medicines Agency Summary of Product Characteristics Pharmacovigilance Validation Drug Master File
54	doi:094471102321616517 Add to Reading List Source URL: escop.com Language: English - Date: 2015-05-22 17:13:33 Botany Pseudoscience Herbalism Medicinal plants Phytotherapy Pharmacovigilance Alternative medicine Draft:European Scientific Cooperative on Phytotherapy Committee on Herbal Medicinal Products
55	ICON Alternative logo CMYK.eps Add to Reading List Source URL: www.aptivsolutions.com Language: English - Date: 2016-06-02 11:26:32 Clinical trials Clinical research Pharmaceutical industry Epidemiology Clinical trial Design of experiments Patient recruitment Pharmacovigilance Medicine Clinical Data Inc Clinical trial portal
56	ACRP_CR_Dec2015_HS_Section.pdf Add to Reading List Source URL: www.acrpnet.org Language: English - Date: 2015-11-23 12:15:01 Clinical research Pharmaceutical industry Clinical trials Clinical research coordinator Good clinical practice Patient recruitment ClinicalTrials.gov Contract research organization Pharmacovigilance Competence Clinical investigator Principal investigator
57	Microsoft Word - GVP遵守通知.doc Add to Reading List Source URL: www.pmda.go.jp Language: English - Date: 2016-07-29 02:05:14 Pharmaceuticals policy Clinical research Clinical pharmacology Drug safety Healthcare quality Pharmacovigilance Clinical trial Medical device Pharmaceutical industry in China Adverse effect
58	CMDh QUESTIONS & ANSWERS PHARMACOVIGILANCE LEGISLATION REGULATION (EU) NOAND DIRECTIVEEU Doc. Ref.: CMDh, Rev.14 OctoberJanuary 2016 Add to Reading List Source URL: www.hma.eu Language: English - Date: 2016-04-20 04:52:35 Pharmaceuticals policy Drug safety Healthcare quality Clinical research Pharmacovigilance Marketing authorization Risk management plan
59	RTF Document Add to Reading List Source URL: esubmission.ema.europa.eu Language: English - Date: 2016-08-19 03:15:41 Clinical research Clinical data management Pharmaceutical industry Pharmaceuticals policy Electronic common technical document Common Technical Document Marketing authorization Validation Pharmacovigilance HTML element Summary of Product Characteristics European Medicines Agency
60	Computational drug repositioning based on side-effects mined from social media Timothy Nugent, Vassilis Plachouras and Jochen L. Leidner Thomson Reuters, Corporate Research and Development, London, United Kingdom ABSTRA Add to Reading List Source URL: peerj.com Language: English - Date: 2016-05-11 09:58:24 Clinical research Clinical pharmacology Pharmacy Clinical trials Pharmacokinetics Pharmacovigilance Adverse effect Drug development Food and Drug Administration Pharmacogenomics Drug interaction