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Food and Drug Administration
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#	Item
91	Experimental Use Exemption of Patent Infringement ̶ A Brief Comparison of China and the United States By: Li Feng, Ph.D., Jiancheng Jiang and Yuan Wang Generally, the purpose of a patent is to award the patentee a limit Add to Reading List Source URL: www.aipf.com Language: English - Date: 2015-10-16 09:12:56 Patent law Law Biotechnology Pharmaceuticals policy Research exemption Health Roche Products Inc. v. Bolar Pharmaceutical Co. United States patent law Merck KGaA v. Integra Lifesciences I Ltd. Patent infringement Generic drug Food and Drug Administration
92	HRPP GUIDELINE 202 Determination of Human Subjects Research Issuing Office: Office of Research Administration Add to Reading List Source URL: www.irb.purdue.edu Language: English - Date: 2014-06-04 09:40:57 Medical research Clinical research ethics Research Applied ethics Medical ethics Clinical research Research ethics Institutional review board Regulatory compliance Human subject research Food and Drug Administration Medical device
93	Processing Steps for Pharmacy Formulary Exception and Review Requests The following processes for review of formulary placement do not replace or supersede existing appeal procedures for step therapy, quantity limits, an Add to Reading List Source URL: hr.uark.edu Language: English - Date: 2016-08-16 16:31:31 Medicinal chemistry Pharmacy Formulary Food and Drug Administration Health
94	Kevin P. Cross, Ph.D. Leadscope, IncDublin Road, Columbus, OH, USA 1 Add to Reading List Source URL: www.leadscope.com Language: English - Date: 2015-11-13 06:28:16 Health Food and Drug Administration Dietary Supplements Dietary Supplement Health and Education Act United States Department of Health and Human Services Didanosine
95	Stanford University HRPP Policy Guidance Humanitarian Use Device (HUD) Add to Reading List Source URL: humansubjects.stanford.edu Language: English - Date: 2016-04-12 01:21:50 Food and Drug Administration Health Ethics Design of experiments Drug safety Humanitarian Device Exemption Institutional review board HDE Hud
96	#233 Guidance for Industry Veterinary Feed Directive Common Format Questions and Answers DRAFT GUIDANCE Add to Reading List Source URL: www.nda.nebraska.gov Language: English - Date: 2016-02-25 11:56:46 Policy Veterinary Feed Directive Government Food and Drug Administration Health
97	Best Practices in Developing Proprietary Names for Drugs Add to Reading List Source URL: www.fda.gov Language: English Health Pharmaceuticals policy Food and Drug Administration Medical research Names Healthcare quality Patient safety United States Adopted Name Prescription Drug User Fee Act Over-the-counter drug Medical prescription International nonproprietary name
98	Some people using buy iressa in canada this medication guide. So with that in mind when evaluating the desirability of including a drug of abuse and you won’t need to be bored. Food and Drug Administration. It helps ke Add to Reading List Source URL: observantnomad.com Language: English - Date: 2016-08-23 19:56:25 Chemistry Organic chemistry Amines Quinazolines Lung cancer AstraZeneca Gefitinib Morpholines Erlotinib Iressa Treatment of cancer Non-small-cell lung carcinoma
99	Sunil Bhonsle Mar 2016 Corporate Presentation Add to Reading List Source URL: c.eqcdn.com Language: English - Date: 2016-04-20 16:56:32 Chemistry Morphinans Neurochemistry Drug rehabilitation Opioid antagonists Organic chemistry Alcohols Euphoriants Buprenorphine Opioid use disorder Methadone Food and Drug Administration
100	Design Considerations and Pre-market Submission Recommendations for Interoperable Medical Devices - Draft Guidance for Industry and Food and Drug Administration Staff Add to Reading List Source URL: www.fda.gov Language: English Health Medicine Medical technology Food and Drug Administration Medical device Medical equipment Investigational device exemption Electronic health record Interoperability Federal Food Drug and Cosmetic Act Interface Biomedical engineering

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