The Medicines (Products for Human Use) (Fees) (Amendment) Regulations 2012 PDF Download
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Author: Great Britain
Publisher:
ISBN: 9780111529171
Category :
Languages : en
Pages : 4
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Book Description
Enabling power: Medicines Act 1971, s. 1 (1) & European Communities Act 1972, s. 2 (2) & Finance Act 1973, s. 56 (1) (2). Issued: 10.10.2012. Made: 04.10.2012. Laid: 10.10.2012. Coming into force: 02.11.2012. Effect: S.I. 2012/504 amended. Territorial extent & classification: E/W/S/NI. General
Author: Great Britain
Publisher:
ISBN: 9780111529171
Category :
Languages : en
Pages : 4
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Book Description
Enabling power: Medicines Act 1971, s. 1 (1) & European Communities Act 1972, s. 2 (2) & Finance Act 1973, s. 56 (1) (2). Issued: 10.10.2012. Made: 04.10.2012. Laid: 10.10.2012. Coming into force: 02.11.2012. Effect: S.I. 2012/504 amended. Territorial extent & classification: E/W/S/NI. General
Author:
Publisher:
ISBN: 9780111520697
Category :
Languages : en
Pages :
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Book Description
Author: Northern Ireland
Publisher:
ISBN: 9780337987472
Category :
Languages : en
Pages : 78
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Book Description
Author: GREAT BRITAIN.
Publisher:
ISBN: 9780111178782
Category :
Languages : en
Pages : 12
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Book Description
Enabling power: European Communities Act 1972, ss. 2 (2) (5). Issued: 24.01.2019. Sifted: -. Made: 14.01.2019. Laid: 18.01.2019. Coming into force: 09.02.2019. Effect: S.I. 2012/1916 amended. Territorial extent & classification: E/W/S/NI. General. EC note: These Regulations amend the Human Medicines Regulations 2012 in order to implement: points 8, 9, 11 and 12 of Article 1 of Directive 2011/62/EU of the European Parliament and of the Council of 8 June 2011 amending Directive 2001/83/EC on the Community code relating to medicinal products for human use, as regards the prevention of the entry into the legal supply chain of falsified medicinal products (Directive 2011/62/EU); Commission Delegated Regulation (EU) 2016/161 of 2 October 2015 supplementing Directive 2001/83/EC of the European Parliament and of the Council by laying down detailed rules for the safety features appearing on the packaging of medicinal products for human use (the Delegated Regulation).
Author: Great Britain
Publisher:
ISBN: 9780111470978
Category : Law
Languages : en
Pages : 8
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Book Description
Enabling power: European Communities Act 1972, s. 2 (2). Issued: 08.12.2008. Made: 03.12.2008. Laid: 08.12.2008. Coming into force: 29.12.2008. Effect: 1968 c. 67 & S.I. 1994/3144; 2008/1692 amended. Territorial extent & classification: E/W/S/NI. General. EC note: These Regulations give effect in the United Kingdom to Regulation No 1901/2006 on medicinal products for paediatric use and amending Regulation No 1768/92, Directive 2001/20/EC, Directive 2001/83/EC and Regulation No 726/2004, as amended by Regulation No 1902/2006 amending Regulation 1901/2006 on medicinal products for paediatric use (the Paediatric Regulation).
Author: Adrian Kilcoyne
Publisher: OUP Oxford
ISBN: 0191510394
Category : Medical
Languages : en
Pages : 473
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Book Description
The breadth of the pharmaceutical medicine can be daunting, but this book is designed to navigate a path through the speciality. Providing a broad overview of all topics relevant to the discipline of pharmaceutical medicine, it gives you the facts fast, in a user-friendly format, without having to dive through page upon page of dense text. With 136 chapters spread across 8 sections, the text offers a thorough grounding in issues ranging from medicines regulation to clinical trial design and data management. This makes it a useful revision aid for exams as well as giving you a taster of areas of pharmaceutical medicine adjacent to your current role. For healthcare professionals already working in the field, this book offers a guiding hand in difficult situations as well as supplying rapid access to the latest recommendations and guidelines. Written by authors with experience in the industry and drug regulation, this comprehensive and authoritative guide provides a shoulder to lean on throughout your pharmaceutical career.
Author: Great Britain: Parliament: Secondary Legislation Scrutiny Committee
Publisher: The Stationery Office
ISBN: 9780108550744
Category : Political Science
Languages : en
Pages : 28
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Book Description
Also includes information paragraphs on 8 instruments
Author: U K Stationery Office
Publisher: Stationery Office/Tso
ISBN: 9780108476228
Category : Law
Languages : en
Pages : 36
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Book Description
Author: American Bar Association. House of Delegates
Publisher: American Bar Association
ISBN: 9781590318737
Category : Law
Languages : en
Pages : 216
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Book Description
The Model Rules of Professional Conduct provides an up-to-date resource for information on legal ethics. Federal, state and local courts in all jurisdictions look to the Rules for guidance in solving lawyer malpractice cases, disciplinary actions, disqualification issues, sanctions questions and much more. In this volume, black-letter Rules of Professional Conduct are followed by numbered Comments that explain each Rule's purpose and provide suggestions for its practical application. The Rules will help you identify proper conduct in a variety of given situations, review those instances where discretionary action is possible, and define the nature of the relationship between you and your clients, colleagues and the courts.
Author: Maria Cristina Galli
Publisher: Springer
ISBN: 3319186183
Category : Medical
Languages : en
Pages : 235
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Book Description
This book discusses the different regulatory pathways for gene therapy (GT) and cell therapy (CT) medicinal products implemented by national and international bodies throughout the world (e.g. North and South America, Europe, and Asia). Each chapter, authored by experts from various regulatory bodies throughout the international community, walks the reader through the applications of nonclinical research to translational clinical research to licensure for these innovative products. More specifically, each chapter offers insights into fundamental considerations that are essential for developers of CT and GT products, in the areas of product manufacturing, pharmacology and toxicology, and clinical trial design, as well as pertinent "must-know" guidelines and regulations. Regulatory Aspects of Gene Therapy and Cell Therapy Products: A Global Perspective is part of the American Society of Gene and Cell Therapy sub-series of the highly successful Advances in Experimental Medicine and Biology series. It is essential reading for graduate students, clinicians, and researchers interested in gene and cell therapy and the regulation of pharmaceuticals.
