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Indian health ministry From Wikipedia, the free encyclopedia   Jump to: navigation, search The Indian Health Ministry is a part of Indian Government and is responsible for provision of health care / health services for all Indian residents. It also has a special department for new drugs approvals. India is entering global pharmaceutical market and these functions of the Indian Health Ministry are pivotal for successful inclusion of India into global health system. External links ICH Website: Guidelines for Clinical Trial Monitoring FDA Website Clinical Research Monitoring Training Clinical Trials Management Careers in Clinical Research Monitoring Clinical Research Monitoring Services Clinical Trial Monitoring Companies Listings International Clinical Research Monitoring and Corporate Trainings Clinical Research Abbreviations and Acronyms Clinical Research Glossary /Definitions List of Food and Drugs Regulatory Agencies Clinical Research: Frequently asked questions

	Learn More About the Biopharmaceutical Industry and Clinical Research: Category: Bioinformatics Biotechnology Biotechnology Companies Cell Imaging Genetic Engineering Genetically Modified Organisms Medicine Molecular Genetics Powered by Wikipedia, the free encyclopedia. Articles were developed by IBPA volunteers.
	A Abbott Laboratories Adverse Drug Reaction Adverse event Almirall Prodesfarma Amgen Approved drugs Assay sensitivity AstraZeneca B Bayer AG Biogen Idec Biopharmaceutical networking Boehringer-Ingelheim Pharmaceuticals C Case Report Form Clinical Trials Budgeting Clinical baseline Clinical investigator Clinical monitoring Clinical protocol Clinical research Clinical research associate Clinical research nurse Clinical site Clinical study design Clinical trial Clinical trial management Confidentiality agreement Contract research organization Contract research organizations Covered clinical study D Double-blind Drug Drug design Drug discovery E Effect size Exclusion criteria F Food and Drug Administration G Genentech GlaxoSmithKline Good Manufacturing Practice Good clinical practice		I Inclusion criteria Informed consent Institute for OneWorld Health Institutional review board International Conference on Harmonisation Investigational product Investigator's Brochure K Kriger Research Center L Life-threatening List of contract research organizations List of pharmaceutical companies M Merck & Co. Multicenter trial N Nonclinical studies Novartis P Patent Pharmaceutical company Pharmaceutical project Pharmacology Placebo Placebo effect Q Quality system R Randomized controlled trial Regulatory requirement S Safety monitoring Serious adverse event Serono Standard Operating Procedures Standard treatment Study population T Teva Pharmaceutical Industries, Ltd.