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MHRA
Results: 841

#	Item
481	CT Form UK 1- Amendment or End of Trial Declaration for a clinical trial that was originally A CTX/DDX application Applicants only need to fill out this form once for each trial (for the first amendment application made Add to Reading List Source URL: www.mhra.gov.uk Language: English - Date: 2010-05-17 10:15:17 Scientific method EudraCT Clinical trial Clinical research Research Science
482	Dates Destination Purpose Add to Reading List Source URL: www.mhra.gov.uk Language: English - Date: 2014-07-09 07:22:03 Department of Health Healthcare in the United Kingdom
483	PDF Document Add to Reading List Source URL: www.mhra.gov.uk - Date: 2008-10-20 09:09:45
484	Risk and Audit Committee attendance April 2010 to March 2011 inclusive Lisa Arnold Michael Fox Vincent Lawton Add to Reading List Source URL: www.mhra.gov.uk - Date: 2011-06-24 09:31:19
485	Dates Destination Purpose Add to Reading List Source URL: www.mhra.gov.uk - Date: 2010-11-24 05:46:37
486	Microsoft Word - EL_07_A13 Final Published Version.doc Add to Reading List Source URL: www.mhra.gov.uk Language: English - Date: 2008-08-25 05:33:39 Sensodyne Diethylene glycol Pharmacist Pharmacy GlaxoSmithKline Toothpaste Pseudoephedrine Dentistry Medicine Health
487	JULY 2013 Formulation switching of antiepileptic drugs A Report on the Recommendations of the Commission on Human Medicines from July 2013 Executive summary This report concerns CHM’s recommendations on issues relating Add to Reading List Source URL: www.mhra.gov.uk Language: English - Date: 2013-12-20 11:14:02 Pharmacology Mood stabilizers Primidone Lamotrigine Phenytoin Carbamazepine Therapeutic drug monitoring Clonazepam Topiramate Anticonvulsants Chemistry Medicine
488	2.1.S DRUG SUBSTANCE 1.1.S.1 General Information 2.1.S[removed]Nomenclature Add to Reading List Source URL: www.mhra.gov.uk Language: English - Date: 2010-03-25 07:30:22 Biology Biotechnology Immune system Monoclonal antibodies Vitamin C Porcine parvovirus Chemistry Medicine Immunology
489	Animal work for the licensing of medicines – the facts This fact sheet explains how animal work is used to test the safety of medicines before they are made available to the public. It takes an average of 10 years from Add to Reading List Source URL: www.mhra.gov.uk Language: English - Date: 2013-12-13 12:57:18 Pharmaceutical industry Clinical research Pharmacology Pharmacy Food and Drug Administration Clinical trial Animal testing Drug discovery New Drug Application Pharmaceutical sciences Science Medicine
490	Safeguarding public health CONTRACT QPs: HOW MUCH IS TOO MUCH? Richard Funnell, Add to Reading List Source URL: www.mhra.gov.uk Language: English - Date: 2010-06-17 10:14:22 Pharmaceutical sciences Copyright law Clinical research Department of Health Medicines and Healthcare products Regulatory Agency Good manufacturing practice Copyright law of the United States Copyright Crown copyright Software Pharmaceutical industry Government

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