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Dale and Appelbe's Pharmacy and Medicines Law

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Dale and Appelbe's Pharmacy and Medicines Law

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In Paperback Format
Dale and Appelbe's Pharmacy and Medicines Law

£54.15
 RRP: £57.00
You save £2.85 (5.0%)
ISBN
9780857112026
Author
Joy Wingfield and Karen Pitchford (eds)
Published by
Pharmaceutical Press
Publication Date
June 2017
Edition
Eleventh edition
Format
Paperback
Extent
588 pages
Dimensions
156 x 234 mm

The eleventh edition of this highly popular book is the definitive guide to law relating to pharmacy and medicine practice. It incorporates material from a wide range of well-known individuals in academia, professional and legal practice and has been fully revised in line with current law and regulation.

The contents to this new edition has been significantly reordered and consolidated. Chapters 2–16 now cover all human medicines legislation, including controlled drugs. Chapter 17 covers legislation on animal medicines and a new chapter 18 consolidates the law on poisons, denatured alcohols and chemicals.

The chapter on controlled drugs and the section on poisons have been completely rewritten to make them more accessible. Information on the Falsified Medicines Directive and pharmacovigilance has been added to all relevant chapters and also commentary on the latest standards and guidance from the General Pharmaceutical Council. The chapter on fitness to practise contains new case law and revised procedural protocols.

Dale and Appelbe's Pharmacy and Medicines Law is an invaluable source for pharmacy undergraduates, pre-registration students and pharmacists in all branches of the profession, as well as anyone who requires knowledge of contemporary British law relating to medicines and poisons and pharmacy professional regulation. 
  1. Sources of law
  2. Human medicines: scope of regulation
  3. Human medicines: the licensing system
  4. Human medicines: advertising
  5. Pharmacy businesses
  6. Human medicines: Pharmacy Medicines
  7. Human medicines: General Sale Medicines
  8. Human medicines: Prescription Only Medicines
  9. Human medicines: exemptions from controls
  10. Human medicines: wholesale dealing
  11. Human medicines: sale and supply of homoeopathic medicines
  12. Human medicines: herbal medicines
  13. Human medicines: prohibitions for protection of the purchaser
  14. Human medicines: labelling, packaging, leaflets and identification
  15. Human medicines: pharmacopoeias and compendia
  16. Controlled Drugs
  17. Veterinary medicines
  18. Poisons, denatured alcohols and chemicals
  19. Miscellaneous legislation affecting pharmacy
  20. Pharmacy regulation
  21. Professional conduct
  22. Fitness to practise
  23. Regulation of health professions
  24. NHS law and organisation
Appendices
  1. Supplementary prescribing: clinical management plan
  2. Patient Group Directions
  3. Schedule 1A to the Poisons Act: Regulated and Reportable Substances
  4. Summary of standards of conduct, ethics and performance (until 1 May 2017)


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