This document summarizes key consumer protection laws and regulatory authorities in Pakistan. It outlines legislation providing protections at the federal level, such as the Islamabad Consumer Protection Act of 1995, and in North-West Frontier Province. It also discusses the Wafaqi Mohtasib (Ombudsman) for addressing consumer complaints. Regulatory authorities overseeing electricity, telecommunications and gas are covered, along with the Pakistan Standards and Quality Control Authority for product standards. The document provides an overview of the consumer protection framework in Pakistan.
Establish Food Safety and Standards Authority of India for laying down science based standards for articles of food and regulate their manufacture, storage, distribution, sale and import, to ensure availability of safe and wholesome food for human consumption.
FSSAI REGULATIONS FOR THE IMPORT, MANUFACTURE AND SALE OF NUTRACEUTICALS IN I...Swapnil Fernandes
- Nutraceutical market has shown steady increase in the last decade.
- The import, manufacture and marketing regulations for nutraceuticals in India have been streamlined with the updation of the FSSAI regulations 2016.
- RDA’s are a collection of values to express a person's nutrient need based on their life stage & gender.
- The RDA recommendations for the Indian population has been provided by the ICMR on the basis of scientific studies and subsequent data generated.
Contents:
History
DRAP
Composition of DRAP
Function of DRAP
Policy board
Funds and budget of DRAP
Real picture of DRAP
Other agencies
References
History Of Authorities
What Is Drug Regulatory Authority
Drug Regulatory Authority of Pakistan (DRAP) has been established in NOV13,2012 for effective coordination and enforcement of the Drugs Act, 1976.
The Drug Regulatory Authority of Pakistan (DRAP) is an autonomous body working under the administrative control of Ministry of National Health Services.
The Authority is expected to regulate, manufacture, import, export, storage, distribution and sale of therapeutic goods.
What Is Drug Regulatory Authority,…
The authority may set up its establishments including sub-offices and laboratories at province capital and such other places from time to time.
The existing Federal Drug Control Administration(FDCA) and sub offices set up in all provinces are called Central Drug Laboratory
For example;
National Control Laboratory on Biological, Karachi
Federal Drug Surveillance Laboratory, Islamabad
Composition Of DRAP
Chief executive officer
Director Pharmaceutical Evaluations and Registration
Director Drug Licensing
Director Quality Assurance and Laboratory Testing
Director Medical Devices and Medicated Cosmetics
Director Biological Drugs
Composition Of DRAP,….
Director Controlled Drugs
Director Health and OTC Products (non-drugs)
Director Costing and Pricing
Director Budget and Accounts
Director Administration, Human Resource and Logistics
Director Legal Affairs
Director Management Information Services
Power And Function Of DRAP
Evaluation and Registration of pharmaceutical drugs, medical devices and medicated cosmetics, alternative medicines And Licensing of Drug Manufacturing facilities.
Regulation of controlled drugs and biological drugs.
Policy board
DRA will work under the Policy board which consists of 15 members.
Chair person of Board will be Secretary of Federal Health Division
Members will consist of Chief Executive of Agency, Health Secretary of all provinces.
Functions of policy board
Monitor and supervise all function of the DRAP.
Approve the budget of the DRAP.
Determine all fees and leaves.
Funds And Budgets
Loans and grants from the national and international agencies received by the federal government and provincial government to finance the function of the authority.
Grat-in aid in term of salaries and retirements benefits of the existing staff provided by the federal government.
Charges and fees collected by the authority to recover the cost of regulated activities
Funds And Budgets……………
Central research fund collected from pharmaceutical industry.
The authority shall, in respect of each financial year prepare an annual budget for approval from board and shall sent to the federal government for appropriate provision and allocation.
Facts About DRAP
Dr Hussein, regional
Establish Food Safety and Standards Authority of India for laying down science based standards for articles of food and regulate their manufacture, storage, distribution, sale and import, to ensure availability of safe and wholesome food for human consumption.
FSSAI REGULATIONS FOR THE IMPORT, MANUFACTURE AND SALE OF NUTRACEUTICALS IN I...Swapnil Fernandes
- Nutraceutical market has shown steady increase in the last decade.
- The import, manufacture and marketing regulations for nutraceuticals in India have been streamlined with the updation of the FSSAI regulations 2016.
- RDA’s are a collection of values to express a person's nutrient need based on their life stage & gender.
- The RDA recommendations for the Indian population has been provided by the ICMR on the basis of scientific studies and subsequent data generated.
Contents:
History
DRAP
Composition of DRAP
Function of DRAP
Policy board
Funds and budget of DRAP
Real picture of DRAP
Other agencies
References
History Of Authorities
What Is Drug Regulatory Authority
Drug Regulatory Authority of Pakistan (DRAP) has been established in NOV13,2012 for effective coordination and enforcement of the Drugs Act, 1976.
The Drug Regulatory Authority of Pakistan (DRAP) is an autonomous body working under the administrative control of Ministry of National Health Services.
The Authority is expected to regulate, manufacture, import, export, storage, distribution and sale of therapeutic goods.
What Is Drug Regulatory Authority,…
The authority may set up its establishments including sub-offices and laboratories at province capital and such other places from time to time.
The existing Federal Drug Control Administration(FDCA) and sub offices set up in all provinces are called Central Drug Laboratory
For example;
National Control Laboratory on Biological, Karachi
Federal Drug Surveillance Laboratory, Islamabad
Composition Of DRAP
Chief executive officer
Director Pharmaceutical Evaluations and Registration
Director Drug Licensing
Director Quality Assurance and Laboratory Testing
Director Medical Devices and Medicated Cosmetics
Director Biological Drugs
Composition Of DRAP,….
Director Controlled Drugs
Director Health and OTC Products (non-drugs)
Director Costing and Pricing
Director Budget and Accounts
Director Administration, Human Resource and Logistics
Director Legal Affairs
Director Management Information Services
Power And Function Of DRAP
Evaluation and Registration of pharmaceutical drugs, medical devices and medicated cosmetics, alternative medicines And Licensing of Drug Manufacturing facilities.
Regulation of controlled drugs and biological drugs.
Policy board
DRA will work under the Policy board which consists of 15 members.
Chair person of Board will be Secretary of Federal Health Division
Members will consist of Chief Executive of Agency, Health Secretary of all provinces.
Functions of policy board
Monitor and supervise all function of the DRAP.
Approve the budget of the DRAP.
Determine all fees and leaves.
Funds And Budgets
Loans and grants from the national and international agencies received by the federal government and provincial government to finance the function of the authority.
Grat-in aid in term of salaries and retirements benefits of the existing staff provided by the federal government.
Charges and fees collected by the authority to recover the cost of regulated activities
Funds And Budgets……………
Central research fund collected from pharmaceutical industry.
The authority shall, in respect of each financial year prepare an annual budget for approval from board and shall sent to the federal government for appropriate provision and allocation.
Facts About DRAP
Dr Hussein, regional
“FUNCTIONAL FOODS: CLAIMS AND LABELING” -- AN OVERVIEW OF THE LAWMichael Swit
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This presentation contains detailed information about the regulatory aspects of food and nutraceuticals a global prospective, which includes WHO guidelines on nutrition and NSF International.
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The first overhaul of the U.S. food manufacturing process in more than 80 years, the federal Food Safety Modernization Act (FSMA) law updates the role of the government in verifying the safety and availability of our food supply. FSMA, as it rolls out, has implications for both domestic manufacturers and those that distribute goods made abroad, in foreign facilities. The Food Institute analyzed the intersection of daily food production and regulatory compliance in this first in a series of 3 presentations on FSMA.
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Consumer Rights Commission of Pakistan (CRCP) is a rights-based civil initiative registered under the Trust Act, 1882. Established in 1998, CRCP is an independent, non-profit, and non-governmental organization. It largely works through local fund-raising and engaging volunteers. It is not supported by any industry or commercial sector. It is the first nationalconsumer organization in the country, which approaches the issue of consumer protection in comprehensive and holistic terms. Its vision and strategies have significant cross linkages with both market practices and issues of governance. CRPC is led by a highly qualified team of professionals and they have worked on the core issues of the consumers' community. The Commission plans to establish its chapters in all provinces to achieve its objectives and members of all walks of life will be included.
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Presentation to the Regulatory Affairs Professionals Society (RAPS) & University of Southern California School of Pharmacy conference on Dietary Supplements & Supplemental Foods." November 2000, Pasadena, CA., covering:
♦ What is a Functional Food
♦ Claims under Nutritional Labeling and Educations Act (NLEA)
♦ FDAMA Claims
♦ FTC Advertising Regulation
This is a try to Minimize the long and lengthy Consumer Protection Act, 2019 of India into a short PPT. I tried to take all the key features from the Act. This Act came into force from 20th July,2020 in India
Presentation to the San Diego Regulatory Affairs Network (SDRAN) RAC Review course; August 2011; covering:
♦ Basics
♦ New Dietary Ingredients
♦ Claims Allowed
♦ GMPs and Other Regulatory Requirements
♦ Adverse Events
The Doha Declaration on the TRIPS Agreement and Public Health was adopted by the WTO Ministerial Conference of 2001 in Doha on November 14, 2001. It reaffirmed flexibility of TRIPS member states in circumventing patent rights for better access to essential medicines
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This presentation contains detailed information about the regulatory aspects of food and nutraceuticals a global prospective, which includes WHO guidelines on nutrition and NSF International.
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The first overhaul of the U.S. food manufacturing process in more than 80 years, the federal Food Safety Modernization Act (FSMA) law updates the role of the government in verifying the safety and availability of our food supply. FSMA, as it rolls out, has implications for both domestic manufacturers and those that distribute goods made abroad, in foreign facilities. The Food Institute analyzed the intersection of daily food production and regulatory compliance in this first in a series of 3 presentations on FSMA.
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Consumer Rights Commission of Pakistan (CRCP) is a rights-based civil initiative registered under the Trust Act, 1882. Established in 1998, CRCP is an independent, non-profit, and non-governmental organization. It largely works through local fund-raising and engaging volunteers. It is not supported by any industry or commercial sector. It is the first nationalconsumer organization in the country, which approaches the issue of consumer protection in comprehensive and holistic terms. Its vision and strategies have significant cross linkages with both market practices and issues of governance. CRPC is led by a highly qualified team of professionals and they have worked on the core issues of the consumers' community. The Commission plans to establish its chapters in all provinces to achieve its objectives and members of all walks of life will be included.
CONSUMER PROTECTION ACT, 1986
It aims at providing better protection of the interests of the consumers.
Act applies to whole of India except Jammu and Kashmir.
The Act applies to all goods and services unless expressly exempted by the Central Government by notification.
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2. CONTENTS
• INTRODUCTION
• CONSUMER PROTECTION LEGISLATION
ISLAMABAD CONSUMER PROTECTION ACT, 1995
NWFP CONSUMER PROTECTION ACT, 1997
• STATE / ADMINISTRATIVE REGULATION
WAFAQI MOHTASIB (OMBUDSMAN) ORDER, 1983
• REGULATORY FRAMEWORKS
NATIONAL ELECTRIC POWER REGULATORY AUTHORITY
PAKISTAN TELECOMMUNICATION AUTHORITY
NATURAL GAS REGULATORY AUTHORITY
• STANDARDS AND QUALITY
PAKISTAN STANDARDS AND QUALITY CONTROL AUTHORITY ACT, 1996
3. Consumer
Consumer is a person or a group who intends to order,
or uses purchased goods, products, or services primarily
for personal, social, family, household and similar needs,
not directly related to entrepreneurial or business
activities.
4. Law
Law is a principle and regulations established in a
community by some authority and applicable to its
people, whether in the form of legislation or of
custom and policies recognized and enforced by state
authority.
5. Reason for Legislation
• To Protect against Poor Quality
• To Stop Unethical Practices
• To See Consumer Justice Is Done
6.
7. Consumer Rights
• Right to Safety
• Right to be Informed
• Right to Choose
• Right to be Heard
• Right to Seek Redress
• Right to Consumer Education
8. Consumer Laws in Pakistan
CONSUMER PROTECTION LEGISLATION
STATE / ADMINISTRATIVE REGULATION
REGULATORY FRAMEWORKS
STANDARDS AND QUALITY
DRUG LAWS
FOOD LAWS
CONSUMER RIGHTS COMMISSION OF PAKISTAN
10. ISLAMABAD CONSUMER PROTECTION ACT, 1995
Nature of the Act:
The Act provides for the promotion and protection of consumer
interests, and the establishment of consumer councils.
Jurisdiction:
Islamabad Capital Territory.
11. Deals with Matters
Protection against marketing of goods which are hazardous
to life and property
The provision of information about the quality, quantity,
potency, purity, standard and price of goods and services
Redress against unfair trade practices of unscrupulous
exploitation of consumers
12. Compensation:
The Court can order for payment of compensation to the consumer to
the extent the consumer has suffered any damage or loss through any
unfair trade practice.
Confiscation of Property:
The Court may order for confiscation of any goods or material or direct
for their destruction to ensure protection of the rights of consumers.
13. NWFP CONSUMER PROTECTION ACT, 1997
Nature of the Act:
To provide for fair commercial practices, promotion and protection of
consumer interests and speedy redress of consumer complaints.
Jurisdiction:
Whole of North West Frontier Province.
14. STATE / ADMINISTRATIVE REGULATION
WAFAQI MOHTASIB (OMBUDSMAN) ORDER, 1983
Nature of the Act:
The Order provides for the appointment of the Wafaqi Mohtasib (Ombudsman) to
diagnose, investigate, redress and rectify any injustice done to a person through
mal- administration.
Jurisdiction:
Whole of Pakistan.
15. LIMITATIONS
A complaint should be made within
three months from the day the
complainant first noticed the
incidence of injustice or mal-
administration. The Mohtasib,
however, can accept cases even
after three months if he thinks it
appropriate under the
circumstances.
16. REGULATORY FRAMEWORKS
NATIONAL ELECTRIC POWER REGULATORY AUTHORITY
PAKISTAN TELECOMMUNICATION AUTHORITY
NATURAL GAS REGULATORY AUTHORITY
17. NATIONAL ELECTRIC POWER REGULATORY AUTHORITY
Jurisdiction:
Pakistan
Functions of the Authority:
The Authority is responsible for providing licenses to electric power
generation, transmission and distribution service providers, regulating
the provision of electric power in Pakistan, setting the terms and
conditions of the licenses, maintaining standards of service, setting tariff,
and if appropriate renewing the license.
18. How many electric companies are in
Pakistan?
There are around 42 independent power producers (IPPs) that contribute
significantly in electricity generation in Pakistan. As of 2016, more than
99% of its population on average has access to electricity.
Punjab is the top region by electricity consumption (million kwh)
in Pakistan.
Faisalabad Electric Supply Company (FESCO)
Islamabad Electric Supply Company (IESCO)
19. PAKISTAN TELECOMMUNICATION AUTHORITY (PTA)
Jurisdiction:
Pakistan
Functions of the Authority:
The Authority is responsible for providing licenses to telecommunication
service providers and regulating the telecommunication sector in Pakistan,
setting the terms and conditions of the licenses, maintaining standards of
service, and if appropriate re-newing the license.
20. Complaints:
Consumers first make a written complaint directly to the service provider by
registered delivery or courier. If the consumer is still not satisfied with the
response, a copy of the written compliant can be attached with the
complaint to the Authority as evidence that the service provider is aware of
the complaint and of their response thereto.
Compensation:
Fine the licensee/service provider up to Rupees three hundred and fifty
million, or
Suspend or terminate the license, impose additional conditions or appoint
an Administrator to manage the affairs of the licensee.
21. NATURAL GAS REGULATORY AUTHORITY
Jurisdiction:
Whole of Pakistan
Nature of Authority:
The Authority is responsible for fostering competition, improving efficiency
of the availability, transportation and distribution of natural gas by
providing licenses to the natural gas providers, regulating their activities,
setting the terms and conditions of the licenses, maintaining standards of
service, and if appropriate renewing/cancelling licenses.
22. Offences:
Any person who undertakes any regulated activity in contravention of this
Ordinance.
If any person, without lawful excuse, willfully or recklessly undertakes any
regulated activity which causes physical damage to the person or property
of another.
If any person does any act with the intention of interfering, without
authorization, with any licensed regulated activity, and thereby causes
damage to any facility, plant, equipment or material employed for such
regulated activity.
23. STANDARDS AND QUALITY
PAKISTAN STANDARDS AND QUALITY CONTROL AUTHORITY ACT,
1996
Jurisdiction:
Whole of Pakistan
Nature of the Act:
To maintain and control quality and standards by granting licenses
and certificates for the use of standard quality, conformity and/or
safety marks in respect of particular article, product or process.
24. Functions of the Authority:
Section 8,10,11,14,20,22
• Registration of inspection agencies
• No person shall use, in relation to any article, product or process or in the
title of any patent or in any trade marks or design the Authority marks
except under a license or certificate issued under this Act.
Penalties
Imprisonment up to 1 year, and/or
Fine not less than 30 thousand rupees, and/or
Forfeiture of any property with respect to which the contravention took
place.