British Pharmacopoeia 2021 [print Edition]
British Pharmacopoeia 2021 [print Edition]

Author: British Pharmacopoeia Commission

Publisher:

Published: 2020-07-30

Total Pages:

ISBN-13: 9780113230846

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Updated annually, the British Pharmacopoeia (BP) is the only comprehensive collection of authoritative official standards for UK pharmaceutical substances and medicinal products. It includes approximately 4,000 monographs which are legally enforced by the Human Medicines Regulations 2012. Where a BP monograph exists, medicinal products or active pharmaceutical ingredients sold or supplied in the UK must comply with the relevant monograph.All monographs and requirements of the European Pharmacopoeia (Ph. Eur.) are reproduced in the BP, making the BP a convenient and fully comprehensive set of standards that can be used across Europe and beyond.

British Pharmacopoeia 2019 [single User Download]
British Pharmacopoeia 2019 [single User Download]

Author: British Pharmacopoeia Commission

Publisher:

Published: 2018-07-30

Total Pages:

ISBN-13: 9780113230716

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Updated annually, the BP is the official, authoritative collection of standards for UK medicinal substances for human and veterinary use. The BP 2015 includes almost 3,500 monographs. All monographs and requirements of the European Pharmacopoeia are also reproduced in the BP, making it an essential reference for students, lecturers and researchers. The online product provides subscribers with access to the British pharmacopoeia 2019, British pharmacopoeia (veterinary) 2019 and the current edition and supplements of Britsh approved names. Concurrent access to the 2014 onwards is also available

The Product Safety and Metrology Etc. (Amendment) Regulations 2021
The Product Safety and Metrology Etc. (Amendment) Regulations 2021

Author: Great Britain

Publisher:

Published: 2021-11-17

Total Pages: 16

ISBN-13: 9780348229158

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Enabling power: European Union (Withdrawal) Act 2018, ss. 8 (1), 8C (1), sch. 7, para. 21 & The Radio Equipment Regulations 2017, reg. 18C (1) (2) (a). Issued: 17.11.2021. Sifted: 02.11.2021. Made: 15.11.2021. Laid: 17.11.2021. Coming into force: 09.12.2021. Effect: S.I. 1977/932; 2001/1701; 2008/1597; 2009/2824; 2010/2617; 2011/1881; 2012/3032; 2014/1638; 2015/1553; 2016/1091, 1092, 1093, 1101, 1105, 1107, 1152, 1153; 2017/737, 1206; 2018/389, 390 amended. Territorial extent & classification: E/W/S/NI. General. EC note: Regulation (EU) 2016/425, 426; Commission Implementing Regulation (EU) 2017/1354 amended

Veterinary Drug Residues
Veterinary Drug Residues

Author: R. J. Heitzman

Publisher: Wiley-Blackwell

Published: 1994

Total Pages: 512

ISBN-13: 9780632037865

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The purpose of this second edition is to bring together the current rapid developments and activities in residues of veterinary drugs within the European Community. The EEC legislation is summarised. There is information on the Reference Laboratories, the Maximum Residues Limits (MRL) and the criteria for the methods to be used for routine analysis of residues by Member States and third countries wishing to export meat to the EC. The current state of examination of residues practised and the analytical methods used in Member States is described in detail. There is a section on quality assurance in the laboratory and also supporting information on residues and chemical/physical data of the most important veterinary drugs

British Pharmacopoeia 2017 [online Edition - Single User Licence]
British Pharmacopoeia 2017 [online Edition - Single User Licence]

Author: British Pharmacopoeia Commission

Publisher:

Published: 2016-08-23

Total Pages:

ISBN-13: 9780113230358

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The British Pharmacopoeia (BP) 2017 supersedes the BP 2016 and becomes legally effective on 1 January 2017. This edition incorporates new BP and European Pharmacopoeia monographs and a significant number of revised monographs. Also included is new information for unlicensed medicines and DNA barcoding. Updated annually, the BP is the only comprehensive collection of authoritative official standards for UK pharmaceutical substances and medicinal products. The BP 2017 includes almost 4,000 monographs which are legally enforced by the Human Medicines Regulations 2012. Where a pharmacopoeial monograph exists, medicinal products sold or supplied in the UK must comply with the relevant monograph. All monographs and requirements of the European Pharmacopoeia are also reproduced in the BP.

Wizards Warp
Wizards Warp

Author: Nick DiLiberto

Publisher: Nick Diliberto

Published: 2021

Total Pages: 62

ISBN-13: 9784600006259

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"Wizards Warp" is Maze Puzzle Book Adventure. Completing each maze progresses you forward on an epic journey to rescue the Princess from the Evil Sorcerers Castle. Each maze has hidden items, such as keys to open doors or magical warp crystals to collect along your journey. Some mazes have multiple exits that will take your journey on alternate paths. Entering the forest can take you over mountains and through the sea or choose the dark and scary cave and face off against the ferocious Spider Queen! There are multiple ways to enjoy your Adventure, so be Brave! be Strong! It is time to enter the WIZARDS WARP! Portal to Maze World!

A Brief Guide to CCC
A Brief Guide to CCC

Author: Julian Busch

Publisher:

Published: 2013-04-13

Total Pages: 86

ISBN-13: 9781484115534

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A Brief Guide to CCC provides a comprehensive overview of the CCC certification. The China Compulsory Certification, also known as CCC or "3C", is the People's Republic of China's mandatory certification system for products imported into or manufactured within the country. The book describes the certification system from audits to product tests and printing options as well as certifying bodies and relevant regulations. It provides insight on how to navigate the system and adequately prepare for the certification process. A Brief Guide to CCC includes a chapter dedicated just to the automotive industry with practical suggestions and useful advice.