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Medicines and Healthcare products Regulatory Agency
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401	SUMMARY MINUTES OF THE CLINICAL TRIALS, BIOLOGICALS & VACCINES (CTBVEAG) EXPERT ADVISORY GROUP HELD ON MONDAY 10 MARCH 2014 Information is being withheld, under Section 43 of the Freedom of Information Act 2000, on the g Add to Reading List Source URL: www.mhra.gov.uk Language: English - Date: 2014-04-16 10:47:47 Drug safety Pharmacovigilance Pharmacy Medicines and Healthcare products Regulatory Agency Commission on Human Medicines Pharmaceutical sciences Pharmacology Health
402	Safeguarding public health through the effective regulation of medicines and medical devices ii Add to Reading List Source URL: www.mhra.gov.uk Language: English - Date: 2012-03-08 11:13:09 Pharmacology Pharmaceutical industry Clinical research Pharmaceuticals policy Pharmacy Medicines and Healthcare products Regulatory Agency Yellow Card Scheme European Medicines Agency General Practice Research Database Medicine Pharmaceutical sciences Health
403	Microsoft Word - PEAG 03 April 2014 FINAL summary report (webminutes) Add to Reading List Source URL: www.mhra.gov.uk Language: English - Date: 2014-05-02 11:42:18 Clinical research Pharmaceutical industry Pharmaceuticals policy Drug safety Medicines and Healthcare products Regulatory Agency Pharmacovigilance Yellow Card Scheme European Medicines Agency Commission on Human Medicines Pharmaceutical sciences Pharmacology Health
404	Microsoft Word - web minutes PEAG meeting held 26 Feb 2014 final UPDATED.doc Add to Reading List Source URL: www.mhra.gov.uk Language: English - Date: 2014-04-07 10:36:07 Clinical research Pharmaceutical industry Pharmaceuticals policy Drug safety European Medicines Agency Pharmacovigilance Medicines and Healthcare products Regulatory Agency Yellow Card Scheme Commission on Human Medicines Pharmaceutical sciences Pharmacology Health
405	Joint Research Compliance Office This is a controlled document. The master document is posted on the JRCO website and any print-off of this document will be classed as uncontrolled. Add to Reading List Source URL: workspace.imperial.ac.uk Language: English - Date: 2012-12-17 09:12:09 Pharmaceutical industry Pharmaceutical sciences Design of experiments Pharmacology Department of Health Medicines and Healthcare products Regulatory Agency Constitutional amendment Clinical trial Institutional review board Clinical research Research Science
406	Transfer of responsibility for the Certificates of Free Sale for medical devices scheme to the Medicines and Healthcare products Regulatory Agency Add to Reading List Source URL: www.gov.uk Language: English - Date: 2013-11-29 09:44:22 Department of Health Health Clinical research Medicines and Healthcare products Regulatory Agency Medical device Medicine Technology Pharmaceutical industry
407	Joint Research Compliance Office This is a controlled document. The master document is posted on the JRCO website and any print-off of this document will be classed as uncontrolled. Add to Reading List Source URL: workspace.imperial.ac.uk Language: English - Date: 2012-12-17 09:16:40 Research Pharmaceutics EudraCT Clinical trial Standard operating procedure Good Clinical Practice Pharmacy Medicines and Healthcare products Regulatory Agency IMP Clinical research Pharmaceutical industry Pharmaceutical sciences
408	Joint Research Compliance Office This is a controlled document. The master document is posted on the JRCO website and any print-off of this document will be classed as uncontrolled. Add to Reading List Source URL: workspace.imperial.ac.uk Language: English - Date: 2012-12-17 09:15:17 Science Pharmaceutical sciences Design of experiments Pharmacology Medicines and Healthcare products Regulatory Agency Clinical trial Good Clinical Practice Institutional review board Protocol Clinical research Research Pharmaceutical industry
409	Joint Research Compliance Office This is a controlled document. The master document is posted on the JRCO website and any print-off of this document will be classed as uncontrolled. Add to Reading List Source URL: workspace.imperial.ac.uk Language: English - Date: 2013-07-08 06:36:01 Pharmaceutical sciences Health Pharmacology Serious adverse event Adverse effect Adverse event Medicines and Healthcare products Regulatory Agency Clinical trial Pharmacovigilance Clinical research Research Pharmaceutical industry
410	Microsoft Word - Strategy Document V 5.doc Add to Reading List Source URL: www.mhra.gov.uk Language: English - Date: 2011-01-12 12:31:22 Health Pharmaceuticals policy Counterfeit consumer goods Clinical research Public health Medicines and Healthcare products Regulatory Agency Counterfeit medications Medical device Counterfeit Pharmaceutical industry Pharmaceutical sciences Medicine

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