Pharmacy Law and Ethics Notes PDF D.Pharm 2nd Year

CHAPTER – 1

  • General Principles of Law, History and various Acts related
  • to Drugs and Pharmacy profession

CHAPTER – 2

  • Pharmacy Act-1948 and Rules: Objectives, Definitions,
  • Pharmacy Council of India; its constitution and functions,
  • Education Regulations, State and Joint state pharmacy
  • councils, Registration of Pharmacists, Offences and Penalties.
  • Pharmacy Practice Regulations 2015

CHAPTER – 3

  • Drugs and Cosmetics Act 1940 and Rules 1945 and New Amendments
  • Objectives, Definitions, Legal definitions of schedules to the Act and Rules Import of drugs – Classes of drugs and cosmetics prohibited from import, Import under license or
  • permit.
  • Manufacture of drugs – Prohibition of manufacture and sale of certain drugs, Conditions for grant of license and conditions of license for manufacture of drugs, Manufacture of drugs for test, examination and analysis,
  • manufacture of new drug, loan license and repacking license.
  • Study of schedule C and C1, G, H, H1, K, P, M, N, and X.
  • Sale of Drugs – Wholesale, Retail sale and Restricted license, Records to be kept in a pharmacy
  • Drugs Prohibited for manufacture and sale in India
  • Administration of the Act and Rules – Drugs Technical
  • Advisory Board, Central Drugs Laboratory, Drugs
  • Consultative Committee, Government analysts, licensing authorities, controlling authorities, Drug Inspectors.

CHAPTER – 4

  • Narcotic Drugs and Psychotropic Substances Act 1985 and Rules Objectives, Definitions, Authorities and Officers, Prohibition, Control and Regulation, Offences and Penalties.

CHAPTER – 5

  • Drugs and Magic Remedies (Objectionable Advertisements) Act 1954
  • Objectives, Definitions, Prohibition of certain advertisements, Classes of Exempted advertisements, Offences and Penalties.

CHAPTER – 6

  • Prevention of Cruelty to Animals Act-1960: Objectives,
  • Definitions, CPCSEA – brief overview, Institutional Animal
  • Ethics Committee, Breeding and Stocking of Animals,
  • Performance of Experiments, Transfer and Acquisition of animals for experiment, Records, Power to suspend or revoke registration, Offences and Penalties.

CHAPTER – 7

  • Poisons Act-1919: Introduction, objective, definition, possession, possession for sales and sale of any poison, import of poisons

CHAPTER – 8

  • FSSAI (Food Safety and Standards Authority of India)
  • Act and Rules: brief overview and aspects related to manufacture, storage, sale, and labelling of Food Supplements

CHAPTER – 9

  • National Pharmaceutical Pricing Authority: Drugs Price
  • Control Order (DPCO) – 2013. Objectives, Definitions, Sale prices of bulk drugs, Retail price of formulations, Retail price and ceiling price of scheduled formulations
  • Pharmaceutical Policy 2002, National List of Essential Medicines (NLEM)

CHAPTER – 10

  • Code of Pharmaceutical Ethics: Definition, ethical principles, ethical problem solving, registration, code of ethics for Pharmacist in relation to his job, trade, medical profession and his profession, Pharmacist’s oath.

CHAPTER – 11

  • Medical Termination of Pregnancy Act and Rules – basic understanding, salient features, and Amendments

CHAPTER – 12

  • Role of all the government pharma regulator bodies – Central Drugs Standards Control Organization (CDSCO),
  • Indian Pharmacopoeia Commission (IPC)

CHAPTER – 13

  • Good Regulatory practices (documentation, licenses, renewals, e-governance) in Community Pharmacy, Hospital pharmacy, Pharma Manufacturing, Wholesale business, inspections, import, export of drugs and medical devices

CHAPTER – 14

  • Introduction to BCS system of classification, Basic concepts of Clinical Trials, ANDA, NDA, New Drug development, New Drugs and Clinical Trials Rules, 2019.
  • Brand v/s Generic, Trade name concept, Introduction to Patent Law and Intellectual Property Rights, Emergency Use Authorization

CHAPTER – 15

  • Blood bank – basic requirements and functions

CHAPTER – 16

  • Clinical Establishment Act and Rules – Aspects related to Pharmacy

CHAPTER – 17

  • Biomedical Waste Management Rules 2016 – Basic aspects, and aspects related to pharma manufacture to disposal of pharma / medical waste at homes, pharmacies, and hospitals

CHAPTER – 18

  • Bioethics – Basic concepts, history and principles.
  • Brief overview of ICMR’s National Ethical Guidelines for Biomedical and Health Research involving human participants

CHAPTER – 19

  • Introduction to the Consumer Protection Act

CHAPTER – 20

  • Introduction to the Disaster Management Act

CHAPTER – 21

  • Medical Devices – Categorization, basic aspects related to manufacture and sale

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