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Pharmaceutical Research
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31	University of New Mexico Cancer Center and New Mexico Cancer Care Alliance Data and Safety Monitoring Plan 2010 Table of Contents Summary................................................................................... Add to Reading List Source URL: cancer.unm-intranet.com Language: English - Date: 2015-06-16 11:46:32 Medical research Clinical research Health Pharmaceutical industry Design of experiments Medical monitoring Clinical pharmacology Clinical trial Cancer and Leukemia Group B Safety monitoring Institutional review board Data monitoring committee
32	Parking Validation Programs Frequently Asked Questions (FAQs) Q: What are the different types of validations offered? A: Downtown, Cinema and Tech Museum validations. Q: Which garages participate in each validation progr Add to Reading List Source URL: parksj.org Language: English - Date: 2015-09-26 01:04:58 Clinical research Pharmaceutical industry Validity Clinical data management Quality Validation Parking Coupon Business
33	TIGes vet Q&A-update - Sept 2013 Add to Reading List Source URL: esubmission.ema.europa.eu Language: English - Date: 2016-08-19 03:16:08 Pharmaceuticals policy Pharmaceutical industry Digital media Research Health Agencies of the European Union Medical research Electronic submission Marketing authorization Heads of Medicines Agencies Electronic common technical document
34	EFPIA Disclosure Code: Your Questions Answered March 2016 #pharmadisclosure www.efpia.eu Add to Reading List Source URL: transparency.efpia.eu Language: English - Date: 2016-05-09 04:01:11 Health care Health Medical research Pharmaceutical industry Clinical research European Federation of Pharmaceutical Industries and Associations Conflict of interest Medical privacy Privacy Clinical trial
35	Global Standard Expectations of Third Parties Add to Reading List Source URL: www.astrazeneca.com Language: English - Date: 2016-03-02 13:23:08 Medical research Business Health Food and Drug Administration Pharmaceutical industry AstraZeneca Sdertlje Municipality Zeneca Clinical trial Mediation Non-disclosure agreement Privacy
36	The Continuous Quality Improvement (CQI) unit (“CQI Team”) is responsible for designing, implementing and maintaining a program Add to Reading List Source URL: humansubjects.stanford.edu Language: English - Date: 2016-04-12 01:21:48 Medical research Health Design of experiments Clinical research Pharmaceutical industry Chartered Quality Institute Clinical trial Audit Certified IRB Professional
37	Pharmaceuticals and Medical Devices Safety Information No. 334 June 2016 Add to Reading List Source URL: www.pmda.go.jp Language: English - Date: 2016-08-03 04:15:08 Medical research Health care Pharmaceuticals policy Health Clinical research Clinical trials Healthcare quality Pharmacovigilance Pharmacy Medical prescription Pharmaceutical industry in China Pharmaceutical industry
38	Food and Drug Administration, HHS § 50.3 PART 50—PROTECTION OF HUMAN SUBJECTS Add to Reading List Source URL: publicfiles.jaeb.org Language: English - Date: 2014-01-30 11:37:23 Medical research Research Clinical research Medical ethics Pharmaceutical industry Food and Drug Administration Investigational device exemption Clinical trial Institutional review board Informed consent Clinical investigator Human subject research
39	Microsoft Word - SOP editedonlineversibaru.doc Add to Reading List Source URL: www.ummc.edu.my Language: English - Date: 2015-06-03 21:28:52 Medical research Clinical research Pharmaceutical industry Institutional review board Clinical trial Good clinical practice Informed consent Adverse event Protocol Ethics committee Serious adverse event University Malaya Medical Centre
40	Annex VI: Implementation of mandatory VNeeS format for Veterinary regulatory submissions <> "Error"Annex VI: Implementation of mandatory VNeeS format for Veterinary regulatory submissions \ MERGEFORMAT Annex VI: Imple Add to Reading List Source URL: esubmission.ema.europa.eu Language: English - Date: 2016-08-19 03:16:08 Pharmaceutical industry Medical research Clinical data management Clinical research Health care Evaluation Validity Quality Validation Marketing authorization Electronic submission

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