|Publishers||R. Narain Publishers & Distributors|
|Author||Dr. Vishal & Rehan Uddin|
|Subject||Text Book of Pharmacy Law & Ethics (In Hindi) (ER2020-26T)|
Text Book of Pharmacy Law & Ethics (In Hindi) (ER2020-26T)
Pharmacy Law & Ethics is a core subject in D. Pharm, which is taught in the second year. It is the branch of pharmacy that deals with the process of converting a novel chemical entity (NCE) or an existing medicine into a medication that patients may use safely and efficiently. It’s also known as dosage form design science where a student learns various techniques of developing a formulation. Many compounds have pharmacological characteristics, but many require specific handling to obtain therapeutically relevant concentrations at their areas of action. Pharmaceutics aids in the connection between medication formulation, distribution and disposal in the body.
Estimated Delivery for Urban Areas 3 to 4 Days
Estimated Delivery for Rural Areas 5 to 7 Days
Table of Content
1 General Principles of Law, History and various Acts related to Drugs and Pharmacy profession
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
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.
4 Narcotic Drugs and Psychotropic Substances Act 1985 and Rules Objectives, Definitions, Authorities and Officers, Prohibition, Control and Regulation, Offences and Penalties.
5 Drugs and Magic Remedies (Objectionable Advertisements) Act 1954 Objectives, Definitions, Prohibition of certain advertisements, Classes of Exempted advertisements, Offences and Penalties.
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.
7 Poisons Act-1919: Introduction, objective, definition, possession, possession for sales and sale of any poison, import of poisons
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
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)
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.
11 Medical Termination of Pregnancy Act and Rules – basic understanding, salient features, and Amendments
12 Role of all the government pharma regulator bodies – Central Drugs Standards Control Organization (CDSCO), Indian Pharmacopoeia Commission (IPC)
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
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
15 Blood bank – basic requirements and functions
16 Clinical Establishment Act and Rules – Aspects related to Pharmacy
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
18 Bioethics – Basic concepts, history and principles. Brief overview of ICMR’s National Ethical Guidelines for Biomedical and Health Research involving human participants
19 Introduction to the Consumer Protection Act.
20 Introduction to the Disaster Management Act.
21 Medical Devices – Categorization, basic aspects related to manufacture and sale.
- Comprehensive coverage of theoretical and diagrammatical aspects of pharmaceutics.
- All intricate aspects are explained by simple, lucid and specific explanations and substantiated with neat and elaborate diagrammatic sketches.
- Examples from pharmaceutics are included extensively.