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Pharmaceutical marketing
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#	Item
51	CMDh_132_2009_Rev38_2015 12_clean Add to Reading List Source URL: www.hma.eu Language: English - Date: 2016-08-02 11:05:45 Pharmaceutical industry Pharmaceuticals policy Summary of Product Characteristics Marketing authorization Test data exclusivity
52	__________________________________________________________________________________________________________ Paul Jones Address Line 1 Address Line 2 London Add to Reading List Source URL: www.cv-service.org Language: English - Date: 2013-10-30 14:57:04 Marketing Business Pharmaceutical marketing Esomeprazole Sales
53	22 JulyJuly 2016 EMAv7.0 User Guidance for Marketing Authorisation Holders (MAHs) for PSUR Repository Add to Reading List Source URL: esubmission.ema.europa.eu Language: English - Date: 2016-08-19 03:16:02 Clinical research Clinical data management Pharmaceutical industry Electronic common technical document Pharmaceuticals policy Marketing authorization Common Technical Document Validation Product lifecycle
54	ETHICS IN DEALING WITH PHARMA INDUSTRIES Dr. Shubhangi R. Parkar1, Dr Trupti F Koli2 ETHICS IN DEALING WITH PHARMA INDUSTRIES Ethics in general is philosophical issue and is defined as philosophical study of morality. Th Add to Reading List Source URL: www.indianjpsychiatry.org Language: English - Date: 2009-08-19 02:44:30 Pharmaceuticals policy Pharmaceutical industry Marketing Pharmaceutical marketing Medical ethics Pharmacy Pharmaceutical industry in China No Free Lunch Medicine Pharmaceutical sales representative Bad Pharma Ethics in pharmaceutical sales
55	Microsoft Word - maporreport_final2.doc Add to Reading List Source URL: www.grady.uga.edu Language: English - Date: 2009-11-09 11:29:20 Marketing Advertising Drugs Clinical pharmacology Pharmaceuticals policy Direct-to-consumer advertising Television advertisement Depository Trust & Clearing Corporation Pharmaceutical marketing Medical prescription Over-the-counter drug Prescription drug
56	Updating ANDA Labeling After the Marketing Application for the Reference Listed Drug Has Been Withdrawn Guidance for Industry Add to Reading List Source URL: www.fda.gov Language: English Food and Drug Administration Pharmaceutical industry Pharmaceuticals policy Food law Abbreviated New Drug Application New drug application Federal Food Drug and Cosmetic Act Generic drug Approved Drug Products with Therapeutic Equivalence Evaluations Center for Drug Evaluation and Research Drug Master File
57	Implementation plan for the introduction of the safety features on the packaging of nationally authorised medicinal products for human use Doc. Ref: CMDhFebruary 2016 Add to Reading List Source URL: www.hma.eu Language: English - Date: 2016-02-19 11:51:17 Pharmaceutical industry Pharmaceuticals policy European Union Clinical data management European Medicines Agency Marketing authorization Closure Validation
58	Association of Pharmaceutical Laboratories for Research and Development Code of Ethics AFIDRO 2015 Add to Reading List Source URL: www.afidro.org Language: English - Date: 2015-02-06 16:51:33 Clinical research Pharmaceutical industry Pharmacy Pharmaceuticals policy Healthcare quality Pharmacovigilance Pharmaceutical marketing Clinical trial Pharmacist Business ethics International Federation of Pharmaceutical Manufacturers & Associations Evidence-based pharmacy in developing countries
59	Rules on the Medicines Act Add to Reading List Source URL: oag.gov.bt Language: English - Date: 2015-04-15 23:30:42 Pharmaceutical industry Pharmaceuticals policy Food and Drug Administration Clinical trial Design of experiments Product testing Good laboratory practice Marketing authorization European Medicines Agency
60	Practical Guidance For the Paper Submission of Regulatory Information in Support of a Marketing Authorisation Application When Using an eCTD or a NeeS as the Source Submission. v2.0 Add to Reading List Source URL: esubmission.ema.europa.eu Language: English - Date: 2016-08-19 03:14:51 Clinical research Clinical data management Electronic common technical document Pharmaceutical industry Pharmaceuticals policy Common Technical Document Marketing authorization Electronic submission Drug Master File