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Qualified person
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341	L[removed]EN Official Journal of the European Union Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:22:07 Health policy Health Clinical Trials Directive Directive 2001/83/EC Good manufacturing practice Qualified Person Good Clinical Practice Directive EudraLex Pharmaceuticals policy Clinical research Research
342	L[removed]EN Official Journal of the European Union Add to Reading List Source URL: www.fve.org Language: English - Date: 2014-06-03 16:50:36 Research Health Pharmacology European Medicines Agency Qualified Person Responsible For Pharmacovigilance Directive 2001/83/EC Pharmacovigilance Qualified Person Summary of Product Characteristics Pharmaceuticals policy Clinical research Pharmaceutical sciences
343	Comments on the Concept Paper submitted for Public Consultation concerning the Delegated Act on Principles and Guidelines of Good Manufacturing Practice for Active Substances in Medicinal Products for Human use. Ref: San Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:41:46 Pharmaceutical sciences Health policy EudraLex Good manufacturing practice Qualified Person Medicinal product Directive 2001/83/EC Validation Qualified Person for Pharmacovigilance Pharmaceuticals policy Clinical research Research
344	CHANGES TO SEC REGULATION D – DISQUALIFICATION OF BAD ACTORS AND LIFTING OF THE BAN ON GENERAL SOLICITATION FREQUENTLY ASKED QUESTIONS 1. Where can one find information as to the events that disqualify a person from be Add to Reading List Source URL: www.ofi.state.la.us Language: English - Date: 2013-11-06 12:14:43 Finance Business Financial regulation 73rd United States Congress Stock market Regulation D Securities Act Security Qualified institutional buyer United States Securities and Exchange Commission United States securities law Financial economics
345	ACCESSIBILITY GUIDELINES FOR GRANTEES Section 504 of the Rehabilitation Act prohibits recipients of federal financial assistance from discriminating against a qualified person with disabilities in any of their programs o Add to Reading List Source URL: www.nationalservice.gov Language: English - Date: 2013-03-20 21:05:14 Ergonomics Transportation planning Urban design Americans with Disabilities Act Section 504 of the Rehabilitation Act Disability Rehabilitation Act United States Knowledge Special education in the United States Law Accessibility
346	Protect Your Pockets: Choosing a Qualified Mortgage Originator One of the biggest investments a person can make is buying a home. In this process, potential homeowners often work with mortgage originators who have to be Add to Reading List Source URL: www.in.gov Language: English - Date: 2014-07-01 03:01:58 Mortgage loan Mortgage fraud Reverse mortgage Business Finance Mortgage broker Certified mortgage planner Mortgage United States housing bubble Consumer fraud
347	Microsoft Word - DGentr-PH-COM_2002_735-F2PH311medicame_EN_ACTE.doc Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:06:39 Research Pharmacology European Medicines Agency Pharmaceutical industry Pharmacovigilance Directive 2001/83/EC Good Laboratory Practice Qualified Person Responsible For Pharmacovigilance EudraLex Clinical research Pharmaceutical sciences Pharmaceuticals policy
348	EUROPEAN COMMISSION HEALTH AND CONSUMERS DIRECTORATE-GENERAL Public health and Risk assessment Pharmaceuticals Brussels, 01 June 2010 Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:30:22 Health Pharmaceutical sciences Pharmaceutical industry Pharmacology EudraLex European Union law Good manufacturing practice Clinical trial Qualified Person Clinical research Pharmaceuticals policy Research
349	Ref. Ares[removed][removed]EUROPEAN COMMISSION HEALTH AND CONSUMERS DIRECTORATE-GENERAL Health systems and products Medicinal products – authorisations, European Medicines Agency Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2013-10-09 09:30:25 Clinical research Pharmacy Drug safety Pharmaceutical industry Pharmacovigilance European Medicines Agency Medicines and Healthcare products Regulatory Agency Medical device Qualified Person Responsible For Pharmacovigilance Pharmaceutical sciences Pharmacology Medicine
350	Patent Ex-partes Decision O[removed] Add to Reading List Source URL: www.ipo.gov.uk Language: English - Date: 2009-12-15 05:03:53 Patent law of the European Union Supplementary protection certificate Research Law Pharmacology Patent law European Medicines Agency Qualified Person Responsible For Pharmacovigilance Pharmaceuticals policy Intellectual property law Clinical research

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