The document summarizes the key aspects of the Pharmacy Act in India, which was enacted in 1948 to regulate the profession of pharmacy. It established the Pharmacy Council of India as the central regulatory body, as well as State Pharmacy Councils. Their main functions include maintaining registers of registered pharmacists, approving pharmacy education institutions and programs, and inspecting pharmacy premises. The Act also defines offenses like practicing pharmacy without registration and their associated penalties. Overall, the Act aims to standardize pharmacy education and practice in India to ensure public health and safety.
The document summarizes the key aspects of the Pharmacy Act of 1948 in India. It outlines the history and objectives of establishing the Act, which was aimed at regulating the profession of pharmacy and ensuring uniform education and training standards. Some key points covered include the constitution of the Pharmacy Council of India and State Pharmacy Councils to oversee education regulations and registration of pharmacists. The roles and functions of these councils are also briefly discussed along with details around the registration process for pharmacists in India.
This document discusses import and export regulations for drugs in India. It provides details on key facts about the Indian pharmaceutical industry, including that India is the largest provider of generic drugs globally. It also outlines the agencies that regulate drug import and export, such as the Central Drugs Standard Control Organisation. The document discusses export and import licensing procedures, quality control and inspection requirements, labeling and packaging standards, and conditions for granting import licenses.
This document provides an overview of the Pharmacy Act of 1948 in India. The key points are:
1. The Pharmacy Act established the Pharmacy Council of India (PCI) as the central regulatory body for pharmacy education and practice. It also established State Pharmacy Councils (SPCs).
2. The PCI and SPCs set standards for pharmacy education, approve pharmacy colleges and courses, maintain registers of pharmacists, promote continuing education, and regulate pharmacy practice.
3. The PCI prescribes regulations for pharmacy programs including admission criteria, curriculum, practical training requirements, and infrastructure standards that colleges must meet.
4. To be registered as a pharmacist, one must have a recognized pharmacy
The Pharmacy Act was enacted in 1948 to regulate the profession of pharmacy in India. It established the Pharmacy Council of India and State Pharmacy Councils to oversee pharmacy education, approve institutions, and maintain registers of pharmacists. The Pharmacy Council of India frames educational regulations, approves courses and examinations, and maintains the central register. State Pharmacy Councils maintain state registers, approve entries and removals of pharmacists, inspect premises, and can remove pharmacists for offenses. The Act also defines key terms and establishes penalties for offenses like falsely claiming to be a pharmacist or dispensing medicines without registration.
medicinal and toilet preparation act 1955.pptHarshadaa bafna
The Medicinal and Toilet Preparation Act of 1955 and Rules of 1976 provide for the levy and collection of excise duties on medicinal and toilet preparations containing alcohol, opium, or other narcotic drugs. It defines key terms and outlines rules for the licensed manufacture of such preparations in bonded or non-bonded facilities. The Act specifies procedures for obtaining alcohol, manufacturing, storing, transporting, and exporting goods. It also describes the powers, duties, and responsibilities of excise officers in implementing and enforcing the Act.
The Drugs and Cosmetics Act, 1940 is an Act of the Parliament of India which regulates the import, manufacture and distribution of drugs in India. The primary objective of the act is to ensure that the drugs and cosmetics sold in India are safe, effective and conform to state quality standards.
The document summarizes the Pharmacy Act of 1948 in India. It establishes the Central Council of Pharmacy to regulate the profession of pharmacy by prescribing minimum education standards. The Council maintains a central register of pharmacists. The Act also creates State Pharmacy Councils to oversee pharmacists at the state level and issue registrations. Its objectives are to regulate and raise the standards of pharmacy education and practice across India.
The document summarizes the key aspects of the Pharmacy Act of 1948 in India. It outlines the history and objectives of establishing the Act, which was aimed at regulating the profession of pharmacy and ensuring uniform education and training standards. Some key points covered include the constitution of the Pharmacy Council of India and State Pharmacy Councils to oversee education regulations and registration of pharmacists. The roles and functions of these councils are also briefly discussed along with details around the registration process for pharmacists in India.
This document discusses import and export regulations for drugs in India. It provides details on key facts about the Indian pharmaceutical industry, including that India is the largest provider of generic drugs globally. It also outlines the agencies that regulate drug import and export, such as the Central Drugs Standard Control Organisation. The document discusses export and import licensing procedures, quality control and inspection requirements, labeling and packaging standards, and conditions for granting import licenses.
This document provides an overview of the Pharmacy Act of 1948 in India. The key points are:
1. The Pharmacy Act established the Pharmacy Council of India (PCI) as the central regulatory body for pharmacy education and practice. It also established State Pharmacy Councils (SPCs).
2. The PCI and SPCs set standards for pharmacy education, approve pharmacy colleges and courses, maintain registers of pharmacists, promote continuing education, and regulate pharmacy practice.
3. The PCI prescribes regulations for pharmacy programs including admission criteria, curriculum, practical training requirements, and infrastructure standards that colleges must meet.
4. To be registered as a pharmacist, one must have a recognized pharmacy
The Pharmacy Act was enacted in 1948 to regulate the profession of pharmacy in India. It established the Pharmacy Council of India and State Pharmacy Councils to oversee pharmacy education, approve institutions, and maintain registers of pharmacists. The Pharmacy Council of India frames educational regulations, approves courses and examinations, and maintains the central register. State Pharmacy Councils maintain state registers, approve entries and removals of pharmacists, inspect premises, and can remove pharmacists for offenses. The Act also defines key terms and establishes penalties for offenses like falsely claiming to be a pharmacist or dispensing medicines without registration.
medicinal and toilet preparation act 1955.pptHarshadaa bafna
The Medicinal and Toilet Preparation Act of 1955 and Rules of 1976 provide for the levy and collection of excise duties on medicinal and toilet preparations containing alcohol, opium, or other narcotic drugs. It defines key terms and outlines rules for the licensed manufacture of such preparations in bonded or non-bonded facilities. The Act specifies procedures for obtaining alcohol, manufacturing, storing, transporting, and exporting goods. It also describes the powers, duties, and responsibilities of excise officers in implementing and enforcing the Act.
The Drugs and Cosmetics Act, 1940 is an Act of the Parliament of India which regulates the import, manufacture and distribution of drugs in India. The primary objective of the act is to ensure that the drugs and cosmetics sold in India are safe, effective and conform to state quality standards.
The document summarizes the Pharmacy Act of 1948 in India. It establishes the Central Council of Pharmacy to regulate the profession of pharmacy by prescribing minimum education standards. The Council maintains a central register of pharmacists. The Act also creates State Pharmacy Councils to oversee pharmacists at the state level and issue registrations. Its objectives are to regulate and raise the standards of pharmacy education and practice across India.
Pharmacy Act –1948: Objectives, Definitions, Pharmacy Council of India; its constitution and functions, Education Regulations, State and Joint state pharmacy councils; its constitution and functions, Registration of Pharmacists, Offences
State pharmacy council and joint state pharmacy council:
Under the Pharmacy Act each Sate Govt. is required to constitute a state pharmacy council for the maintenance of register of Pharmacists of the State and to monitor their professional activities.
Two or more states can also enter into an agreement to form a Joint State Pharmacy Council.
The document discusses the Pharmacy Act of 1948 and provides definitions and details regarding:
- The objectives of establishing the Pharmacy Council of India to regulate pharmacy education and practice.
- The constitution and functions of the Pharmacy Council of India and State Pharmacy Councils, including prescribing education standards and maintaining registration of pharmacists.
- The registration process for pharmacists, including qualifications for entry on the first and subsequent registration registers.
The document summarizes the Prevention of Cruelty to Animals Act 1960 in India. It outlines the objectives of preventing unnecessary pain/suffering to animals. It defines key terms and outlines the roles and guidelines of Institutional Animal Ethics Committees and the Committee for the Control and Supervision of Experiments on Animals in regulating experiments and care of animals. Infractions are subject to penalties like fines or imprisonment. The overall aim is to ensure humane treatment of animals used in experiments and activities.
The Pharmacy Act of 1948 was enacted to regulate the profession of pharmacy in India by establishing the Pharmacy Council of India and State Pharmacy Councils. The objectives of the Act were to raise the standards of pharmacy education and practice. It provides for the registration of pharmacists, defines minimum qualifications, and establishes regulations regarding pharmacy education. The Act also outlines offenses and penalties for violations to protect public health.
A presentation aimed at providing information with regards to the Pharmacy Act, 1948.
-INTRODUCTION
-HISTORY OF THE ACT
-PHARMACY COUNCIL OF INDIA
-STATE PHARMACY COUNCIL
-SPECIAL PROVISIONS OF THE ACT
-OFFENCES AND PENALTIES
-CONCLUSION
-REFERENCES
Pharmaceutical Legislations – A brief review, Introduction, Study of drugs enquiry committee, Health survey and development committee, Hathi committee and Mudaliar committee
4 medicinal and toilet preparation act 1955Charudatta Jog
This document outlines the Medicinal & Toilet Preparation Act of 1955, which was passed to standardize excise duties across states in India. The key objectives of the act were to levy and collect duties on alcohol used in medicinal and toilet preparations and curb irregularities. The act established procedures for licensing the manufacture of preparations containing alcohol or narcotics. It also differentiated between manufacturing processes that took place within bonded laboratories versus outside of them, and outlined exemptions, duties, and responsibilities of excise officers in enforcing the act.
The document outlines a code of pharmaceutical ethics to guide pharmacists in their profession. It discusses ethics, morality, and law as they relate to pharmacy. The code is meant to guide pharmacists in their job duties, trade practices, relationships with other medical professionals and the public, and responsibilities to their profession. Specifically, it addresses proper conduct in dispensing medications, fair business practices, limitations of professional activities, and maintaining professional vigilance and adherence to laws. Overall, the code provides moral and ethical guidance for pharmacists to follow in their work and interactions with others.
This document contains 25 multiple choice questions regarding the Pharmacy Act of 1948 in India. The questions cover topics like the objective of the Pharmacy Act, the establishment of the Pharmacy Council of India in 1949, functions and roles of the Central and State pharmacy councils, registration requirements for pharmacists, offenses and penalties under the Pharmacy Act. An answer key is provided at the end listing the correct response for each question.
The Drug & Magic Remedies Act 1954 aims to control advertisements of drugs and prohibit advertisements of remedies alleged to possess magic qualities. It defines key terms like advertisement and magic remedy. It prohibits advertisements for certain medical purposes and those that are misleading. It also prohibits magic remedy advertisements for specified diseases. Exempted advertisements include those approved by the government and literature sent to doctors. Violations can result in fines and imprisonment. Notable cases include action against a baba advertising magic treatments and conviction of a company MD for herbal aphrodisiac ads.
The document summarizes the key aspects of the Pharmacy Act of 1948 in India. It established the Central Council of Pharmacy to regulate the profession and prescribe minimum education standards. The Act also created State Pharmacy Councils to maintain registers of qualified pharmacists. Only those with recognized qualifications can be registered and legally dispense medicines. The Act aims to standardize pharmacy education and training, and regulate those practicing in the field to protect public health.
History and Objectives
Definitions
Administration of the act and rules
Provisions related to Import
Provisions related to Manufacture
Provisions related to Sale
Labeling and Packaging
Schedules to the act and rules
Recent amendment act, 2008
List of forms
This document summarizes the key points of the Medicinal & Toilet preparations act of 1955 and rules thereunder from 1976 regarding the production of medicines and toiletries containing alcohol or other substances. It defines key terms, outlines the licensing process for bonded and non-bonded laboratories, and describes the requirements for facilities. Offenses and penalties are also specified for licensees, excise officers, and the public. The overall objective is to regulate the use of substances like alcohol in medical and personal care products through a licensing and inspection process, as well as by defining illegal activities and associated penalties.
WHO and ICH Guidelines for the Assessment of Herbal Drugijtsrd
The medicinal plant and herbal drugs products are widely used for thousands of years in all over the parts of the world. The word herbal drugs denoted plant parts or plants.That is converted into phytopharmaceuticals by means of straight forward processes including harvesting, drying, and storage. In recent few decades, growth and recognition of herbal medicine and plant products have taken a big share of healthcare.Theres the increasing awareness and general acceptability of the use of herbal drugs in todays practice Although, most of these applications are unorthodox, its however known fact that all over 80 of the world population are depends on herbal medicine and products for healthy living Where standardization and control with proper integration of recent scientific techniques and lore is incredibly important. This rise within the utilization of herbal product has also given to numerous forms of adulteration and abuse of the products leading to consumers and manufacturers disappointment. The challenge is innumerable and making the worldwide herbal market unsafe Evaluation of herbal drug showing an important and vital tool within the formulation of high quality herbal products. Herbal drug technology mainly used for converting botanical materials into medicines. Ms. Bhadane Suvarna | Dr. Takarkhede Smita | Ms. Kakade Pooja | Ms. Jaiswal Sangeeta | Ms. Kanaujiya Shreya | Ms. Khan Alqama "WHO & ICH Guidelines for the Assessment of Herbal Drug" Published in International Journal of Trend in Scientific Research and Development (ijtsrd), ISSN: 2456-6470, Volume-6 | Issue-3 , April 2022, URL: https://www.ijtsrd.com/papers/ijtsrd49571.pdf Paper URL: https://www.ijtsrd.com/pharmacy/other/49571/who-and-ich-guidelines-for-the-assessment-of-herbal-drug/ms-bhadane-suvarna
The document summarizes the key aspects of the Medicinal and Toilet Preparations Act and Rules, 1955 in India. The objectives of the act are to provide for excise duties on medicinal and toilet preparations containing alcohol, narcotics or drugs and to control their manufacture and misuse. The act defines relevant terms and outlines the licensing process and requirements for the manufacture of such preparations both within bonded premises and outside. It also describes the duties and powers of excise officers, search and seizure procedures, offenses and penalties. The schedule lists the categories of dutiable goods and applicable rates of duty.
This document summarizes the Drugs and Magic Remedies Act 1954 which aims to control advertisements of drugs and prohibit advertisements for remedies claiming magic qualities. Some key points:
- It defines terms like advertisement, drug, and magic remedy. Advertisements of certain drugs are prohibited for diseases like AIDS that require medical consultation.
- Advertisements cannot be misleading or make false claims. Advertising magic remedies for treating diseases is also prohibited.
- Some exemptions exist like signs by doctors, scientific books, and ads to doctors if following certain conditions.
- Offences can be punished by imprisonment up to 6 months or 1 year for subsequent offences. Forfeiture of unlawful advertisements and protection from legal
Objectives, Definitions, Pharmacy Council of India; its constitution and functions, Education Regulations, State and Joint state pharmacy councils; constitution and functions, Registration of Pharmacists, Offences and Penalties
The Pharmacy Act of 1948 was enacted to regulate the profession of pharmacy in India by establishing the Pharmacy Council of India and state pharmacy councils. The objectives were to raise the standards of pharmacy education and practice. The Act defines terms like registered pharmacist and provides for the registration and regulation of pharmacists. It established the Pharmacy Council of India as the central regulatory body and state pharmacy councils. The councils were tasked with maintaining registers of pharmacists, approving educational institutions and programs, and investigating complaints. The Act also outlined offenses and penalties for practicing pharmacy without registration or obstructing council inspectors.
Pharmacy Act –1948: Objectives, Definitions, Pharmacy Council of India; its constitution and functions, Education Regulations, State and Joint state pharmacy councils; its constitution and functions, Registration of Pharmacists, Offences
State pharmacy council and joint state pharmacy council:
Under the Pharmacy Act each Sate Govt. is required to constitute a state pharmacy council for the maintenance of register of Pharmacists of the State and to monitor their professional activities.
Two or more states can also enter into an agreement to form a Joint State Pharmacy Council.
The document discusses the Pharmacy Act of 1948 and provides definitions and details regarding:
- The objectives of establishing the Pharmacy Council of India to regulate pharmacy education and practice.
- The constitution and functions of the Pharmacy Council of India and State Pharmacy Councils, including prescribing education standards and maintaining registration of pharmacists.
- The registration process for pharmacists, including qualifications for entry on the first and subsequent registration registers.
The document summarizes the Prevention of Cruelty to Animals Act 1960 in India. It outlines the objectives of preventing unnecessary pain/suffering to animals. It defines key terms and outlines the roles and guidelines of Institutional Animal Ethics Committees and the Committee for the Control and Supervision of Experiments on Animals in regulating experiments and care of animals. Infractions are subject to penalties like fines or imprisonment. The overall aim is to ensure humane treatment of animals used in experiments and activities.
The Pharmacy Act of 1948 was enacted to regulate the profession of pharmacy in India by establishing the Pharmacy Council of India and State Pharmacy Councils. The objectives of the Act were to raise the standards of pharmacy education and practice. It provides for the registration of pharmacists, defines minimum qualifications, and establishes regulations regarding pharmacy education. The Act also outlines offenses and penalties for violations to protect public health.
A presentation aimed at providing information with regards to the Pharmacy Act, 1948.
-INTRODUCTION
-HISTORY OF THE ACT
-PHARMACY COUNCIL OF INDIA
-STATE PHARMACY COUNCIL
-SPECIAL PROVISIONS OF THE ACT
-OFFENCES AND PENALTIES
-CONCLUSION
-REFERENCES
Pharmaceutical Legislations – A brief review, Introduction, Study of drugs enquiry committee, Health survey and development committee, Hathi committee and Mudaliar committee
4 medicinal and toilet preparation act 1955Charudatta Jog
This document outlines the Medicinal & Toilet Preparation Act of 1955, which was passed to standardize excise duties across states in India. The key objectives of the act were to levy and collect duties on alcohol used in medicinal and toilet preparations and curb irregularities. The act established procedures for licensing the manufacture of preparations containing alcohol or narcotics. It also differentiated between manufacturing processes that took place within bonded laboratories versus outside of them, and outlined exemptions, duties, and responsibilities of excise officers in enforcing the act.
The document outlines a code of pharmaceutical ethics to guide pharmacists in their profession. It discusses ethics, morality, and law as they relate to pharmacy. The code is meant to guide pharmacists in their job duties, trade practices, relationships with other medical professionals and the public, and responsibilities to their profession. Specifically, it addresses proper conduct in dispensing medications, fair business practices, limitations of professional activities, and maintaining professional vigilance and adherence to laws. Overall, the code provides moral and ethical guidance for pharmacists to follow in their work and interactions with others.
This document contains 25 multiple choice questions regarding the Pharmacy Act of 1948 in India. The questions cover topics like the objective of the Pharmacy Act, the establishment of the Pharmacy Council of India in 1949, functions and roles of the Central and State pharmacy councils, registration requirements for pharmacists, offenses and penalties under the Pharmacy Act. An answer key is provided at the end listing the correct response for each question.
The Drug & Magic Remedies Act 1954 aims to control advertisements of drugs and prohibit advertisements of remedies alleged to possess magic qualities. It defines key terms like advertisement and magic remedy. It prohibits advertisements for certain medical purposes and those that are misleading. It also prohibits magic remedy advertisements for specified diseases. Exempted advertisements include those approved by the government and literature sent to doctors. Violations can result in fines and imprisonment. Notable cases include action against a baba advertising magic treatments and conviction of a company MD for herbal aphrodisiac ads.
The document summarizes the key aspects of the Pharmacy Act of 1948 in India. It established the Central Council of Pharmacy to regulate the profession and prescribe minimum education standards. The Act also created State Pharmacy Councils to maintain registers of qualified pharmacists. Only those with recognized qualifications can be registered and legally dispense medicines. The Act aims to standardize pharmacy education and training, and regulate those practicing in the field to protect public health.
History and Objectives
Definitions
Administration of the act and rules
Provisions related to Import
Provisions related to Manufacture
Provisions related to Sale
Labeling and Packaging
Schedules to the act and rules
Recent amendment act, 2008
List of forms
This document summarizes the key points of the Medicinal & Toilet preparations act of 1955 and rules thereunder from 1976 regarding the production of medicines and toiletries containing alcohol or other substances. It defines key terms, outlines the licensing process for bonded and non-bonded laboratories, and describes the requirements for facilities. Offenses and penalties are also specified for licensees, excise officers, and the public. The overall objective is to regulate the use of substances like alcohol in medical and personal care products through a licensing and inspection process, as well as by defining illegal activities and associated penalties.
WHO and ICH Guidelines for the Assessment of Herbal Drugijtsrd
The medicinal plant and herbal drugs products are widely used for thousands of years in all over the parts of the world. The word herbal drugs denoted plant parts or plants.That is converted into phytopharmaceuticals by means of straight forward processes including harvesting, drying, and storage. In recent few decades, growth and recognition of herbal medicine and plant products have taken a big share of healthcare.Theres the increasing awareness and general acceptability of the use of herbal drugs in todays practice Although, most of these applications are unorthodox, its however known fact that all over 80 of the world population are depends on herbal medicine and products for healthy living Where standardization and control with proper integration of recent scientific techniques and lore is incredibly important. This rise within the utilization of herbal product has also given to numerous forms of adulteration and abuse of the products leading to consumers and manufacturers disappointment. The challenge is innumerable and making the worldwide herbal market unsafe Evaluation of herbal drug showing an important and vital tool within the formulation of high quality herbal products. Herbal drug technology mainly used for converting botanical materials into medicines. Ms. Bhadane Suvarna | Dr. Takarkhede Smita | Ms. Kakade Pooja | Ms. Jaiswal Sangeeta | Ms. Kanaujiya Shreya | Ms. Khan Alqama "WHO & ICH Guidelines for the Assessment of Herbal Drug" Published in International Journal of Trend in Scientific Research and Development (ijtsrd), ISSN: 2456-6470, Volume-6 | Issue-3 , April 2022, URL: https://www.ijtsrd.com/papers/ijtsrd49571.pdf Paper URL: https://www.ijtsrd.com/pharmacy/other/49571/who-and-ich-guidelines-for-the-assessment-of-herbal-drug/ms-bhadane-suvarna
The document summarizes the key aspects of the Medicinal and Toilet Preparations Act and Rules, 1955 in India. The objectives of the act are to provide for excise duties on medicinal and toilet preparations containing alcohol, narcotics or drugs and to control their manufacture and misuse. The act defines relevant terms and outlines the licensing process and requirements for the manufacture of such preparations both within bonded premises and outside. It also describes the duties and powers of excise officers, search and seizure procedures, offenses and penalties. The schedule lists the categories of dutiable goods and applicable rates of duty.
This document summarizes the Drugs and Magic Remedies Act 1954 which aims to control advertisements of drugs and prohibit advertisements for remedies claiming magic qualities. Some key points:
- It defines terms like advertisement, drug, and magic remedy. Advertisements of certain drugs are prohibited for diseases like AIDS that require medical consultation.
- Advertisements cannot be misleading or make false claims. Advertising magic remedies for treating diseases is also prohibited.
- Some exemptions exist like signs by doctors, scientific books, and ads to doctors if following certain conditions.
- Offences can be punished by imprisonment up to 6 months or 1 year for subsequent offences. Forfeiture of unlawful advertisements and protection from legal
Objectives, Definitions, Pharmacy Council of India; its constitution and functions, Education Regulations, State and Joint state pharmacy councils; constitution and functions, Registration of Pharmacists, Offences and Penalties
The Pharmacy Act of 1948 was enacted to regulate the profession of pharmacy in India by establishing the Pharmacy Council of India and state pharmacy councils. The objectives were to raise the standards of pharmacy education and practice. The Act defines terms like registered pharmacist and provides for the registration and regulation of pharmacists. It established the Pharmacy Council of India as the central regulatory body and state pharmacy councils. The councils were tasked with maintaining registers of pharmacists, approving educational institutions and programs, and investigating complaints. The Act also outlined offenses and penalties for practicing pharmacy without registration or obstructing council inspectors.
The Pharmacy Act of 1948 was introduced to regulate the profession of pharmacy in India by restricting practice to those with adequate education. It established the Pharmacy Council of India to regulate pharmacy education and approve courses. State Pharmacy Councils were also formed in each state. The Act defined key terms and outlined the objectives, functions and regulatory powers of the central and state councils regarding pharmacy education, registration of pharmacists, inspection of premises and enforcement. It aimed to protect public health by ensuring only qualified professionals practiced pharmacy.
The document discusses the Pharmacy Act of 1948 which was enacted to regulate the profession of pharmacy in India by establishing the Pharmacy Council of India and provincial pharmacy councils, requiring the registration of pharmacists, and setting minimum education standards. It outlines the objectives of the Act, definitions, constitution and functions of the councils, qualifications and process for registering pharmacists, and penalties for offences.
The document summarizes the Pharmacy Act of 1948 in India. It provides a history of the Act, noting a lack of regulation previously led to unqualified persons practicing pharmacy. The Act established the Pharmacy Council of India to regulate pharmacy education and practice. It also allows for state pharmacy councils to oversee registration of pharmacists and ensure minimum education standards. The Act defines penalties for practicing pharmacy without registration and outlines registration requirements and processes to ensure only qualified professionals practice in India.
The Pharmacy Act of 1948 was enacted to regulate the practice of pharmacy in India by establishing the Pharmacy Council of India and State Pharmacy Councils. The Act defines "pharmacist" and outlines registration requirements including qualifications. It also establishes renewal fees and penalties for offenses like practicing pharmacy without registration. The Councils are responsible for registering pharmacists, approving educational institutions and programs, and maintaining the register of pharmacists in their state/country.
The Pharmacy Act in India is a legislation that provides the legal framework for the regulation of pharmacy practice in the country. It sets out the requirements for the registration and licensing of pharmacists, as well as the standards of education and training that pharmacists must meet in order to practice. It also establishes regulatory bodies such as the Pharmacy Council of India and the State Pharmacy Councils, which oversee and enforce the law.
The Pharmacy Act in India also includes provisions related to the sale and distribution of drugs and other pharmaceutical products, as well as regulations concerning the operation and management of pharmacies. It defines the various roles and responsibilities of pharmacists, including dispensing and compounding medications, providing patient counseling and education, and collaborating with other healthcare providers.
Overall, the Pharmacy Act in India aims to ensure the safety and efficacy of pharmaceutical care in the country by providing a legal framework for the regulation of pharmacy practice.
The pharmacy act 1948 explained in the easiest form with tricks and tips to learn. The act is about the practice of pharmacy in India. It provides with knowledge of skill and training of the personnel called pharmacists.
The Pharmacy Act of 1948 was enacted to regulate the profession of pharmacy in India by establishing the Pharmacy Council of India and State Pharmacy Councils. The key objectives were to provide uniform pharmacy education across states, maintain registration of pharmacists, and raise the overall standards of pharmacy practice. The Act introduced provisions for approving pharmacy colleges, maintaining central and state registers of pharmacists, and penalties for offenses like practicing pharmacy without registration. It aimed to professionalize pharmacy and protect public health by restricting dispensing of medicines to registered pharmacists only.
The Pharmacy Act of 1948 aims to regulate the profession of pharmacy in India. It established the Pharmacy Council of India (PCI) and State Pharmacy Councils (SPC) to oversee pharmacy education and registration of pharmacists. The PCI frames regulations for pharmacy education, approves courses and institutions, and maintains the central register of pharmacists. SPCs prepare and maintain state registers. The Act also defines qualifications for registration as a pharmacist and penalties for offenses like practicing pharmacy without registration.
History, Objectives, Various Definitions, The Pharmacy Council of India (PCI), Functions and duties of PCI, State Pharmacy Council, Functions of The State PharmacyCouncils, Joint State Pharmacy Council, Offences and penalties and List of amending Acts and adaptation orders.
The document summarizes the key aspects of the Pharmacy Act of 1948 in India. It established the Pharmacy Council of India (PCI) and State Pharmacy Councils (SPC) to regulate pharmacy education and practice. The PCI prescribes minimum education standards and approves pharmacy programs and qualifications. SPCs maintain registers of pharmacists in their state. Only registered pharmacists can dispense medicines or run drug stores. The Act aims to professionalize pharmacy through education, registration and restricting practice to qualified pharmacists.
pharmacy act 1948 .
An Act to regulate the profession of pharmacy. WHEREAS it is expedient to make better provision for the regulation of the profession and practice of pharmacy and for that purpose to constitute Pharmacy Councils; It is hereby enacted as follows:—
The Pharmacy Act of 1948 was implemented to regulate the practice of pharmacy in India by establishing the Pharmacy Council of India and State Pharmacy Councils. The objectives were to provide uniform education and training standards, maintain registration of pharmacists, and regulate the profession. Key points include:
- PCI prescribes minimum education standards and maintains the central register of pharmacists.
- State councils register local pharmacists, inspect premises, and submit reports to PCI.
- Regulations define qualifications, registration process, removal from registers, and penalties for violations.
The aim of presentation is to provide information related to pharmacy Act, 1948.
Introduction
Definition
Pharmacy Council of India
State pharmacy Council
Registration of pharmacists
Offences and penalties
This PPT Covers Pharmacy Act –1948: Objectives, Definitions, Pharmacy Council of India; its
constitution and functions, Education Regulations, State and Joint state pharmacy
councils; constitution and functions, Registration of Pharmacists, Offences and Penalties
(I) In India previously, there were no restrictions on practicing pharmacy and people without proper education in pharmacy were practicing it. This was harming public health.
(II) To regulate the profession, the Pharmacy Bill was introduced in 1947 and passed in 1948 as the Pharmacy Act. This act established the Central Council of Pharmacy to set education standards and approve courses for pharmacists.
(III) The Act requires a minimum level of professional education to practice pharmacy, protects the title of pharmacist, and establishes state pharmacy councils to maintain registers of qualified pharmacists.
(I) In India previously, there were no restrictions on practicing pharmacy and people without proper education in pharmacy were practicing it. This was harming public health.
(II) To regulate the profession, the Pharmacy Bill was introduced in 1947 and passed in 1948 as the Pharmacy Act. This act established the Central Council of Pharmacy to set education standards and approve courses for pharmacists.
(III) The Act requires a minimum level of education to register as a pharmacist and practice pharmacy. State Pharmacy Councils were also formed to maintain registers of qualified pharmacists.
The Pharmacy Council of India (PCI) regulates the profession of pharmacy in India through the Pharmacy Act of 1948. The PCI was established on March 4, 1948 as the statutory body to oversee pharmacy. State Pharmacy Councils (SPCs) were also formed to register pharmacists at the state level and maintain registers of pharmacists. The Pharmacy Act establishes the PCI and SPCs, outlines their composition and responsibilities, and defines offenses and penalties related to practicing pharmacy without registration.
The document discusses the history and regulations around pharmacy practice and education in India. It describes how the Pharmacy Council of India was established in 1949 to regulate the profession through various functions like maintaining central registers of pharmacists, setting minimum education standards, and approving pharmacy courses and institutions. State pharmacy councils were also formed and are responsible for registering pharmacists within each state based on educational qualifications. The regulations and qualifications for registration have evolved over time as the profession became more formalized.
Empowering ACOs: Leveraging Quality Management Tools for MIPS and BeyondHealth Catalyst
Join us as we delve into the crucial realm of quality reporting for MSSP (Medicare Shared Savings Program) Accountable Care Organizations (ACOs).
In this session, we will explore how a robust quality management solution can empower your organization to meet regulatory requirements and improve processes for MIPS reporting and internal quality programs. Learn how our MeasureAble application enables compliance and fosters continuous improvement.
Healthy Eating Habits:
Understanding Nutrition Labels: Teaches how to read and interpret food labels, focusing on serving sizes, calorie intake, and nutrients to limit or include.
Tips for Healthy Eating: Offers practical advice such as incorporating a variety of foods, practicing moderation, staying hydrated, and eating mindfully.
Benefits of Regular Exercise:
Physical Benefits: Discusses how exercise aids in weight management, muscle and bone health, cardiovascular health, and flexibility.
Mental Benefits: Explains the psychological advantages, including stress reduction, improved mood, and better sleep.
Tips for Staying Active:
Encourages consistency, variety in exercises, setting realistic goals, and finding enjoyable activities to maintain motivation.
Maintaining a Balanced Lifestyle:
Integrating Nutrition and Exercise: Suggests meal planning and incorporating physical activity into daily routines.
Monitoring Progress: Recommends tracking food intake and exercise, regular health check-ups, and provides tips for achieving balance, such as getting sufficient sleep, managing stress, and staying socially active.
Can Allopathy and Homeopathy Be Used Together in India.pdfDharma Homoeopathy
This article explores the potential for combining allopathy and homeopathy in India, examining the benefits, challenges, and the emerging field of integrative medicine.
Letter to MREC - application to conduct studyAzreen Aj
Application to conduct study on research title 'Awareness and knowledge of oral cancer and precancer among dental outpatient in Klinik Pergigian Merlimau, Melaka'
International Cancer Survivors Day is celebrated during June, placing the spotlight not only on cancer survivors, but also their caregivers.
CANSA has compiled a list of tips and guidelines of support:
https://cansa.org.za/who-cares-for-cancer-patients-caregivers/
Stem Cell Solutions: Dr. David Greene's Path to Non-Surgical Cardiac CareDr. David Greene Arizona
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1. THE PHARMACYACT
( An act to regulate profession of pharmacy )
Mr. Amitkumar K. Jadhav
Keshavrao Patil Institute of
Pharmacy
2. CONTENT --
History of Pharmacy Act.
Objectives
Definitions
The Pharmacy Council Of India and
it’s functions-
Design of the educational pattern
Approval of Institutions/withdrawal of approvals
Maintenance of Central Register of Pharmacists
State Pharmacy Council and it’s
functions
Maintenance of registers
Entry and removal of names
Removal of name from registers
Printing of Registers
Inspection by State Council
Offences and Penalties
2
3. HISTORY OF PHARMACY ACT-
In India there was no any restriction to
practice the profession of pharmacy.
Hundred of case were found by government
wherein the compounding, mixing or
dispensing of medicines was being done by
persons who were not adequately
educated in this line.
These causing great harm to the health of
people.
It was found necessary to enact a law for
the regulation of the profession and
practice of pharmacy.
An act was promulgated in 1948 entitled
the pharmacy act 1948.
3
4. OBJECTIVE-
Toregulate the pharmacy education in
the country for the purpose of
registration as a pharmacist under the
pharmacy act.
They also regulate the profession.
practice of pharmacy.
4
5. Definitions
-“PharmacyAct” –An act to regulate
the profession of pharmacy.
“Registered Pharmacist”- A person
whose name is for the time being
entered in the register of the state in
which he or she is for the time being
residing or carrying on his profession
or business of pharmacy.
5
6. THE PHARMACY COUNCIL OF INDIA-
The first pharmacy council of
India(P.C.I) constituted by central
government in 1949.
It is reconstituted every 5 years.
A. Constitution,office Bearers
etc.: It consists of three diffirent
types of members-
1. Elected member
2. Nominated member
3. EX-Officio Member
6
7. 1.Elected members-
.
A. 6 members(teachers),elected by
University Grant Commission(UGC).
There is at least one teacher of each of
the
pharmacy, pharmaceutical
chemistry, pharmacognosy and
pharmacology.
B.One member,elected by Medical
Council of India.
C.One member, elected by State
Council,who shall be a
registered pharmacist. 7
8. 2. Nominatedmembers-
.
A. 6 member,nominated by the Central
Government. Of whom at least 4 shall
be persons possessing a degree or
diploma in, and practicing pharmacy,or
pharmaceutical chemistry.
B.A representative of the U.G.C. and
a representative of theAll India
Councilfor Technical
Education(A.I.C.T.E.)
C.One member nominated by each
State Government,who shall be a
registered pharmacist. 8
9. 3. Ex-OfficioMembers-
A.. The Director general of Health Services.
B. The Director of Central Drug Laboratory.
C. The Drug controller of India.
Executive Committee Consisting of-
President
Vice – President
(President and Vice – President of Central
Council shall be elected by the members of
the Council from themselves.)
Five members elected by Central Council
from it’s members.
9
11. The elected and nominated members of
thecouncil hold office for a period of 5
years,but they can resign their
membership at any time,by writing to
the president of the council.
All members are eligible for re-election
of re-nomination.
11
12. B.FUNCTIONS--
Design of the educational pattern—
Toframe an educational stracture for the
would be pharmacist and to keep it
tuned to the changing needs with
passage of time .
The standards of education for
pharmacist framed by the council are
known as the Educational
Regulations and amongst other
things prescribe.As-
Minimum qualification for admission to
the course.
12
13. Duration of the training and the course
of
.
study to be covered.
Equipments and facilities to be
provided by the institutions.
Giving practical training.
Holding approved examinations.
(After the formation of the state
councils the State Government were
supposed to publicize the Education
Regulations in the States in
consultation with the respective State
13
14. .
Approval of Institutions/withdrawal
of approvals:
o An institution or authority,which conducts
a course of study or hold an examination
for the pharmacists, has to apply to the
Pharmacy Council of India for approval of
the course or the examination.
o The council may depute its inspectors to
visit the institution to check whether the
prescribed facilities for imparting training
or holding examinations are in
accordance with the Education
Regulations or not.
14
15. o It may also require inspectors to attend
any
e. xamination,to judge its standard
without interfering with its conduct.
o The Inspectors then report to the
council.
o If on the report of the Inspector, the
council is satisfied then it gives approval
to it and then the said course or
examination shall be deemed to be
approved for qualifying for registration
as pharmacist under the act.
o If any approved course of study or
examination does not continue to be in
conformity with the Education
Regulations, then the council withdraw
15
16. Maintenance of Central Register
ofP.
harmacists
:o Under the provision of the pharmacy
(Amendment)Act 1976, the Pharmacy
Council of India is required to maintain
a register containing names of all
persons registered as pharmacists in
diffirent states.
o This register has to maintained by
the registrar of the Council and
has to be revised suitably from
time to time and published in the
Gazette of India. 16
17. STATE PHARMACY COUNCIL-
It also consists of three diffirent types of
members- Elected, nominated andex-
officio.
A. Elected members-
Six members, elected from amongst
themselves by registered pharmacist of
the state.
One member elected from amongst
themselves by the member of each
Medical Council of the State.
17
18. B. Nominated members–
F.
ive members,of whom at least three
shall be possessing a degree or
diploma in pharmacy or
pharmaceutical chemistry or to be
registered pharmacists, nominatedby
the state government.
C. Ex-OfficioMembers-
Chief administrative medical officer of
the state.
Government Analyst nominated by
state government under the drug and
cosmetic act 1940.
Officer in charge of drugs
control organization of the
1
8
19. Where two or more States enter into
an agreement to form a joint State
Pharmacy Council:
Registered pharmacist – 3 to 5 from
each state instead of 6 in the single
State Council.
Government Nominees – 2 to 4 from
each State instead of 5.
Medical Council Nominee – one from
each State.
Chief Administrative Medical Officer,
GovernmentAnalyst and Officer- in –
charge,Drug Control - Ex-officio
from each state.
19
20. .Each Council shall have a president
and vice-president, elected by the
members from amongst themselves
provided that for five years from the
first constitution of the council.
The president will be nominated by the
State Government and if he is not
already a member, he becomes a
member of the council in addition.
The State Council are, before the end
of June in each year,required to pay to
the PCI a sum of equivalent to one-
fourth of the fees.
20
21. B. FUNCTIONS OF THE STATE PHARMACY
COUNCILS:
Maintenance of registers-
The Register shall include the
following particulars namely-
The full name and residential address
of the registered person.
The date of his/her first admission to
the register.
His/her qualifications for registration.
His professional address,and if he is
employed by any person, the name of
such person.
21
22. ENTRY AND REMOVAL OFNAMES:
After an appointed date, all
applications for registration should be
addressed to the registrar of the State
Pharmacy Council.
The applicant has the requisite
qualifications for registration, he may
direct his or her name to be entered in
the register.
Person whose names have been
removed from the registers of other
State shall not be entitled to
registration unless the State Council
22
23. Upon entry of the name of person in the
.
register,the Registrar is required to
issueto him a certificate of registration
in the prescribed form.
On payment of the fees, the registrar is
required to issue a receipt thereof and
such receipts are deemed to be proofs
of renewal of registration.
23
24. REMOVAL OF NAME FROMTHE
REGISTER:
The name of a pharmacist may be
removed from the register on following
counts-
If his name has been entered in
register by error.
If he has been convicted of an offence in
any professional.
Any pharmacist ,who is held guilty and
whose name has been removed from
register,shall continue to remain a
registered pharmacist for the next three
months and only after the expiry of that
period he shall cease to be a registered
pharmacist. 24
25. A person aggrieved by the order
directingt.
he removal of his name, may appeal
totheState Government within 80 days
whose decision shall be final.
A person whose name has been
removed from the register, is required to
surrender his certificate of registration
to the registrar of the Pharmacy Council
concerned.
If it feels that the offence was a minor
nature, it may warn the pharmacist and
stop the consideration of his case for a
specified period, during which the
pharmacist should prove himself to be
of good behavior. 25
26. .
But in cases of serious professional
neglector criminal conviction, his name
maybe removed.
Pharmacist can, however appeal to the
high court against the decision of
Statutory Committee.
26
27. Printing of
Registers-The Register of the State Pharmacy
Council were required to publish the
Registers on the first April
following the beginning of the
Pharmacy(Amendment) Act.
Later on, each year after the first of
April, they were to publish
supplements to the Registers showing
all additions or changing.
These Registers and supplements
are deemed to be proof that the
persons, whose name are
contained therein,are registered
27
28. Inspection by State Council:
The State Pharmacy Council have
been empowered to appoint suitable
number of Inspectors having
prescribed qualifications to inspect
premises where drugs are dispensed
or compounded.
28
30. Offence
s
1) Falsely claiming
to be a registered
pharmacist.
2) Dispensed by
unregistered
person.
Exception-medical
practitioner.
3) Failure to surrender
certificate of
registration.
4) Obstructing
State Pharmacy
Council
Inspectors.
Penalties
1.a) Fine up to Rs.
500.00on
first conviction.
b)Fine up to Rs.1000.00
and/or 6 months
imprisonment of any
subsequent conviction.
2) 6 months
imprisonment or fine
up
to range 1000.00 or
Both.
3) Fine up to
Rs.50.00
4) 6 months
30