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Download or read book The Assessors Collectors and Town Clerks Manual Containing a Full and Accurate Exposition of the Law Relating to the Powers and Duties of These Officers with an Appendix of Forms written by Isaac Grant Thompson and published by BoD – Books on Demand. This book was released on 2024-06-23 with total page 282 pages. Available in PDF, EPUB and Kindle. Book excerpt: Reprint of the original, first published in 1876.

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Download or read book The Municipal Manual part I Containing The Municipal Act R S O C 223 and the Amending Acts of 1898 1899 and 1900 Viz 61V C 23 62V 1st Session Cc 2 and 5 62V 2nd Session Cc 26 and 30 and 63V Cc 9 33 35 36 and 37 with Notes of Cases Bearing Thereon written by Charles Robert Webster Biggar and published by . This book was released on 1900 with total page 1188 pages. Available in PDF, EPUB and Kindle. Book excerpt:

Download or read book Catalogue of Printed Books written by British Museum. Department of Printed Books and published by . This book was released on 1950 with total page 936 pages. Available in PDF, EPUB and Kindle. Book excerpt:

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Download or read book Guide to EU Pharmaceutical Regulatory Law written by Sally Shorthose and published by Kluwer Law International B.V.. This book was released on 2017-02-17 with total page 590 pages. Available in PDF, EPUB and Kindle. Book excerpt: In the European Union (EU) and its Member States, as elsewhere, the marketing of pharmaceuticals has become subject to an increasingly complex web of legislation and regulation, resulting from the intense scrutiny necessary to ensure such essential products are not only efficacious but safe. This useful volume lays out this system with extraordinary clarity and logic. Adopting a Europe-wide perspective on the law governing pharmaceuticals, expert authors from the law firm Bird & Bird LLP map the life cycle of a medicinal product or medical device from development to clinical trials to product launch and ongoing pharmacovigilance, offering comprehensive and unambiguous guidance at every stage. A brief overview of how the proposed exit from the EU by the UK will affect the regulatory regime is also included. Following an introductory overview focusing on the regulatory framework for pharmaceuticals in Europe – from its underlying rationales to the relevant committees and agencies – each of fifteen incisive chapters examines a particular process or subject. Among the many topics and issues covered are the following: - obtaining a marketing authorisation; - stages and standards for creating a product dossier; - clinical trials; - how and when an abridged procedure can be used; - criteria for conditional marketing authorisations; - generic products and ‘essential similarity’; - paediatric use and the requisite additional trials; - biologicals and ‘biosimilars’; - homeopathic and herbal medicines; - reporting procedures; - pharmacovigilance; - parallel trade; - relevant competition law and intellectual property rights; and - advertising. In addition, national variation charts in many of the chapters illustrate eight major jurisdictions (Belgium, France, Germany, Italy, The Netherlands, Spain, Sweden, and the UK). Sample forms and URLs for the most important Directives are included. Pharmaceutical lawyers and regulatory advisers, both in-house and in private practice, will welcome this unique book. It offers immeasurable value for all who need to understand the process of bringing a medicinal product or medical device to market and the continuing rights and obligations.