Medicinal and toilatory preparation act 1955 Suvarta Maru
This document discusses the Medicinal and Toilet Preparation Act of 1955 and related rules from 1976 regarding the production and regulation of alcoholic preparations in India. It outlines key definitions including bonded and non-bonded manufactories. There are two modes of manufacturing preparations containing alcohol - in bond, using untaxed alcohol under excise supervision, or outside bond using taxed alcohol. The licensing process and ideal facility requirements are described. Responsibilities of excise officers who oversee the facilities and powers granted to them are also summarized.
in that presentation information regarding how to start pharmaceutical acts in all over India & also provides history of pharmaceutical legislation in India
This presentation is related to the drug price control order in India. It will give an idea to the readers how the prices have been fixed for the formulations. How the price has been calculated for scheduled formulations.
This act gives an idea about the constitution and functions of PCI. Brief about Education Regulation in India. Registration procedure for the pharmacist in India.
The document discusses pharmaceutical legislation in India. It outlines the origin of pharmaceutical companies in India in the early 19th century. In 1931, the Drug Enquiry Committee was appointed to investigate the drug market and make recommendations. The committee recommended establishing drug control departments, a central drug laboratory, and pharmacy councils. This led to the Drug Act of 1940 and subsequent acts regulating drug import, manufacture, and sale. The objective of pharmaceutical legislation is to ensure public access to safe, effective drugs.
Drugs and magic remedies act 1954 and rules Rupali Bhoje
This document outlines the Drugs and Magic Remedies (Objectionable Advertisements) Act of 1954 in India. The key points are:
- It prohibits advertising of drugs for certain purposes like abortion, contraception, and treatment of diseases listed in a schedule like cancer, tuberculosis, etc.
- Advertising is also banned for "magic remedies" that claim to treat diseases through charms or rituals.
- Exemptions are provided for certain advertisements directed at medical professionals with prior government approval.
- Penalties are defined for violations which include fines and imprisonment on conviction.
The document summarizes the constitution and functions of key organizations under the Drugs and Cosmetics Act of 1940 and Rules of 1945 in India. The Drugs Technical Advisory Board (DTAB) advises the central and state governments and consists of 18 ex-officio and nominated members. The Drugs Consultative Committee (DCC) advises on securing uniformity and consists of central and state government representatives. The Central Drugs Laboratory (CDL) in Kolkata analyzes drug and cosmetic samples sent by courts and customs and maintains reference standards.
Medicinal and toilet preparations act and rules,1955 (excise duties)Niveditha Shankar
The document summarizes the Medicinal and Toilet Preparations Act and Rules of 1955 in India. The key points are:
1) The Act provides for uniform excise duties on medicinal and toilet preparations containing alcohol, opium, cannabis, or other narcotics throughout India.
2) Manufacturing such preparations requires a license from excise authorities and following strict rules regarding facilities, storage, record keeping and excise oversight.
3) Excise duties are collected when preparations containing alcohol or narcotics are removed from licensed manufacturing premises, with some exemptions for charitable facilities. Penalties are prescribed for violations.
The document summarizes key aspects of the Drug and Cosmetic Act and Rules in India, including:
- The Acts and Rules regulate the import, manufacture, distribution and sale of drugs and cosmetics in India.
- Important definitions are provided for terms like "drug", "cosmetic", "manufacture" and others.
- Drugs and cosmetics can be deemed "misbranded", "adulterated" or "spurious" if they do not meet certain standards.
- The Rules contain 18 parts and 26 schedules providing detailed requirements and guidelines for drugs and cosmetics.
- Key agencies like the Drugs Technical Advisory Board help administer the Acts and
The document discusses the history and development of pharmaceutical legislation in India. It notes that legislation was first introduced under British rule to regulate the import of medicines. In 1931, the Chopra Committee was formed to recommend a comprehensive drug law, which led to the Drugs and Cosmetics Act of 1940. The committee also recommended establishing drug laboratories and a pharmacopoeia. Later committees like the Bhore Committee further strengthened standards for pharmacists. The Hathi Committee covered aspects like licensing and price control. Overall the document provides an overview of key events and committees that shaped pharmaceutical regulation in India.
The Drugs and Magic Remedies (Objectionable Advertisements) Act, 1954 prohibits false or misleading advertisements related to drugs or magic remedies. It defines terms like "drug" and "advertisement" and sets rules around advertising drugs for conditions like miscarriage or sexual pleasure. The Act establishes penalties for violations and gives powers to authorize officers to inspect and seize non-compliant advertisements. It aims to protect consumers from objectionable or misleading claims in drug advertising.
The prevention of cruelty to animals act 1960Shaik Rasheed
This presentation give the complete information regarding the The Prevention of Cruelty to Animals Act 1960 including the definitions, composition of IAEC, Breeding and stocking of animals, experiments, offences and penalties.
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.
This presentation includes an brief idea about the pharmacy act 1948 in India and also deals with its the chapter that included in the act.(Education Regulations, PCI, State PCI, Registration of Pharmacist , Approval of Institutions, Offences penalties etc.)
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
Bonded laboratories are suitable for large-scale manufacture of goods and require supervision from excise staff. They must have four distinct compartments and pay excise duty when goods are removed. Non-bonded laboratories are suitable for small-scale manufacture without excise staff oversight. They require three compartments and pay excise duty upon purchase of raw spirits. Advance security money is needed for bonded laboratories but not for non-bonded ones, though state governments can relax infrastructure requirements for low alcohol production.
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.
National Pharmaceutical Pricing Authority and DPCO 2013Ashish Chaudhari
This document discusses drug regulation in India. It provides an overview of the key bodies that govern drug regulation, including the Central Drug Standard Control Organization and the National Pharmaceutical Pricing Authority. The NPPA was established in 1997 to fix and revise prices of controlled drugs and formulations. The document outlines the objectives of the Drug Price Control Order and its schedules for essential medicines. It also explains the process for determining ceiling prices and maximum retail prices of scheduled drug formulations in India.
The government has notified the DPCO 2013 under the Essential Commodities Act, 1955, which will give power to the NPPA (National Pharmaceutical Pricing Authority (NPPA )to regulate prices of 348 essential drugs along with their specified strengths and dosages under NLEM 2011.
The document discusses India's Drug Price Control Order (DPCO) which allows the government to regulate prices of essential drugs. The objectives of the DPCO are to ensure adequate production and supply of drugs at fair prices through equal distribution. It defines key terms like bulk drugs, formulations, and ceiling prices. The DPCO specifies how maximum retail prices are calculated and requires manufacturers to provide drug cost information to the government annually. It also outlines penalties for violating the order, such as increasing prices without approval or selling drugs in unlabeled split quantities.
This document provides an overview of the Drugs and Magic Remedies Act 1954 in India. The key points are:
1. The Act aims to control advertisements related to drugs that make false claims or mislead the public, and to prohibit advertisements for magic remedies claiming treatment of certain diseases.
2. It defines terms like "advertisement", prohibits misleading drug advertisements and advertisements for magic remedies, and lists exempted advertisements.
3. Offenses under the Act are punishable with imprisonment or fines, and it also regulates import/export of banned advertisements. The schedule lists diseases that cannot be claimed to treat through uncontrolled advertisements.
This document summarizes the key aspects of the Drugs and Magic Remedies (Objectionable Advertisements) Act 1954 in India. The objectives of the act are to control advertisements related to drugs and prohibit advertisements related to magic remedies that make false claims. It defines advertisement, magic remedies, drugs, and registered medical practitioners. It outlines six classes of prohibited advertisements and six classes of exempted advertisements. It discusses offenses and penalties for non-compliance and provides miscellaneous details like the process for scrutinizing misleading ads and obtaining prior government sanction.
This document outlines classes of prohibited and exempted drug advertisements under the law. It defines advertisement and drugs. Classes of prohibited advertisements include those promoting miscarriage, menstrual disorders, sexual pleasure, or unapproved treatments. Exempted advertisements include those printed by the government, sent to registered medical practitioners, or complying with conditions like including therapeutic indications and precautions. Contraventions are punishable by imprisonment, fines, or both.
This document summarizes the Drugs and Magic Remedies (Objectionable Advertisements) Act 1954 in India. The key points are:
1. The Act aims to control advertisement of drugs in certain cases and prohibit advertisements for remedies alleged to possess magic qualities or that claim treatment of certain diseases.
2. It defines terms like "advertisement", "magic remedy", "drug" and prohibits advertisements of drugs for treating diseases like miscarriage or sexual disorders.
3. The Act also prohibits misleading drug advertisements and those referring to magic remedies for treating specified diseases. It establishes penalties for violations.
The Drugs and Magic Remedies Act prohibits advertisements of drugs that make false claims or advertise remedies for certain conditions. It also bans advertisements for magic remedies. The objectives are to maintain ethical standards in drug advertising and ban ads that offend morality or claim magical powers. The Act defines key terms and prohibits ads for drugs related to miscarriage, sexual pleasure, or incurable diseases. Exempted ads include those in scientific journals or distributed only to medical professionals. The Act gives powers of search, seizure and penalties for violations.
The Drug and Magic Remedies Act of 1954 was passed to regulate advertisements of drugs and magic remedies in India by prohibiting advertisements that promote self-medication or treatment of certain diseases, as well as those that mislead people about drugs. The Act defines key terms like advertisement and drug, outlines classes of prohibited and exempted advertisements, and establishes penalties for violations, with increased punishment for repeat offenses. The objective is to control advertisements related to drugs and prohibit misleading advertisements of magic remedies that falsely claim to cure diseases.
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 Drug and Magic Remedies Act of 1954 aims to control drug advertising and prohibit advertisements for magic remedies. Key points:
- It prohibits advertisements of drugs used for abortion, contraception, or sexual pleasure, as well as misleading drug ads. Magic remedy ads for specified diseases are also banned.
- Exempted advertisements include signs at registered medical practitioners' offices and information in bona fide scientific publications. Ads providing therapeutic, administration, dosage and side effect information to practitioners are also allowed.
- Diseases that cannot be claimed cured include blindness, AIDS, goiter, tuberculosis, high blood pressure, sexual problems, cancer, epilepsy, paralysis and menstrual disorders.
- Penalties for violating the
DRUGS AND MAGIC REMEDIES OBJECTIONABLE ADVERTISEMENTS.pptxGAMPA kumar
The Drugs and Magic Remedies (Objectionable Advertisements) Act of 1955 controls advertising of drugs in India and prohibits advertisements of drugs for certain purposes like procuring miscarriage or improving sexual pleasure. It also prohibits advertisements containing false claims about drugs. The Act defines key terms like "drug" and "magic remedy" and specifies exempted advertisements like those directed at doctors from its prohibitions. Contraventions of the Act may be punished with fines or imprisonment.
This document outlines the key provisions of an act to control certain types of drug advertisements and prohibit advertisements for magic remedies. It defines key terms like advertisement, magic remedy, and drug. It describes classes of prohibited advertisements such as those claiming treatment for miscarriage, menstrual disorders, or sexual pleasure. It also lists exempted advertisements such as those published by the government, sent to doctors, or in scientific publications. The document concludes by outlining offenses and penalties under the act.
The Drugs and Magic Remedies (Objectionable Advertisements) Act, 1954 is an Act of the Parliament of India which controls advertising of drugs in India. It prohibits advertisements of drugs and remedies that claim to have magical properties, and makes doing so a cognizable offence.
The Drug and Magic Remedies (Objectionable Advertisements) Act of 1954 aims to control advertisements relating to drugs and prohibit advertisements of magic remedies that falsely claim to cure diseases. The Act defines drugs, advertisements, and magic remedies. It prohibits advertisements of drugs for inducing abortion, contraception, or sexual pleasure, as well as those claiming to treat diseases listed in a schedule. Exempted are advertisements approved by the government, those sent to doctors, and those in scientific publications. Contraventions are punishable by fines and imprisonment.
This document outlines regulations regarding advertisements for drugs and magic remedies in India. It defines key terms like advertisement, drug, and magic remedy. It prohibits advertisements for drugs used for abortion, contraception, or sexual pleasure. It also bans ads for magic remedies claiming to treat serious diseases. Exempted are ads approved by the government, scientific publications, and signs at registered medical practitioners' offices. The penalties for violating these prohibitions include fines and imprisonment.
Study of salient features of drugs and magic remedies act and its rulesKhushbooVerma63
The document summarizes key aspects of the Drugs and Magic Remedies Act and its rules in India. It defines key terms like advertisement, drug, and magic remedy. It prohibits advertisements for certain drugs and magic remedies for diseases listed in a schedule. It exempts some advertisements with government permission or sent to doctors. It outlines penalties for violations, including fines and imprisonment. It discusses offenses by companies and provides a case study about action against a "baba" advertising magic treatment.
The Drugs and Magic Remedies (Objectionable Advertisements) Act, 1954 prohibits false or misleading advertisements related to drugs or magic remedies. It defines terms like "drug" and "advertisement" and sets rules around advertising drugs for conditions like miscarriage or sexual pleasure. The Act establishes penalties for violations and gives powers to authorize officers to inspect and seize non-compliant advertisements. It aims to protect consumers from objectionable or misleading claims in drug advertising. Company representatives can also be held liable unless the offense was committed without their knowledge.
This document summarizes the key aspects of the Drugs and Magic Remedies Act and its rules in India. The act aims to control advertising of drugs and prohibit advertising of remedies with alleged magic qualities. It defines terms like advertisement, magic remedy, and drug. It prohibits advertising of drugs for certain diseases and disorders, misleading drug advertisements, and magic remedy advertisements. It exempts certain types of advertisements including those by the government or with permission. Offenses by companies and penalties are also outlined. A case study of a company convicted for violating the act is provided.
This document outlines exemptions and provisions for advertisements related to drugs and remedies under the Drugs and Magic Remedies (Objectionable Advertisements) Act 1954. It lists 5 classes of advertisements that are exempt from being prohibited, including those printed by the government, sent confidentially to doctors, or relating to books on diseases. It also describes conditions for certain exempted advertisements, such as those in medical journals only including therapeutic information. Penalties are described for violating the Act, including fines or imprisonment. Authorities may also scrutinize misleading drug advertisements and require information from manufacturers.
The Drugs and Magic Remedies (Objectionable Advertisements) Act 1954 aims to control advertisement of drugs and prohibit advertisements of remedies with magical qualities. Key points:
1. It defines terms like drugs, advertisements and magic remedies.
2. It prohibits advertisements of drugs for diseases like miscarriage and sexual disorders. Also bans misleading drug ads.
3. The Act prohibits ads of magic remedies for certain diseases and bans import/export of prohibited advertisements.
4. It includes a schedule listing 54 diseases that drug ads cannot claim treatment for without approval.
Similar to Drugs and magic Remedies, Act 1954 (20)
Anti -fungal agents(PHARMACEUTICAL CHEMISTRY)P.N.DESHMUKH
This documents discuss introduction of anti fungal agents , its classification and
Several classes of anti fungal agents, including polyenes like amphotericin B and azoles. Key information on amphotericin B is provided, including its mechanism of action, uses, administration, and adverse effects.
They work by disrupting the fungal cell membrane or inhibiting fungal enzyme activity.
Introduction to Medical device(PHARMACY LAW AND ETHICS)P.N.DESHMUKH
Ministry of Health and Family Welfare, (MHFW) Government of India, in consultation with
Drugs Technical Advisory Board (DTAB), brought in Medical Devices Rules 2017 in conformity with Global Harmonization Task Force (GHTF) framework and conform to best international practices.
This presentation explain the medical device, its classification, documents required for license of medical device.
NEW DRUG APPLICATION( PHARMACY LAW AND ETHICS)P.N.DESHMUKH
NDA is an important component of approval process. It provides following information and data for review.
1. Chemical and Pharmaceutical data.
2. Information and data of Phase I, Phase II and Phase III of clinical trials.
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INTRODUCTION TO BIOPHARMACEUTICS CLASSIFICATION SYSTEMP.N.DESHMUKH
The Biopharmaceutics Classification System is a system to differentiate the drugs on the basis of their solubility and permeability.
Classification of drugs as per BCS system include
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New drug development process(PHARMACY LAW AND ETHICS)P.N.DESHMUKH
New Drug development process is a Process of bringing a new pharmaceutical drug to the market once a lead compound has been identified through the process of drug discovery.
Drug development process
include
1. Discovery & development
2. Preclinical Research
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Prevention of cruelty to animals act,1960P.N.DESHMUKH
Prevention of Cruelty to Animals Act-1960 includes 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
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This PPT covers drug therapy for tuberculosis. It includes classification of antitubercular drugs.
First line agents like Rifampin/Rifampicin
Isoniazide
Pyrazinamide
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Para amino-salicyclic acid
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CODE OF PHARMACEUTICAL ETHICS (PHARMACY LAW AND ETHICS)P.N.DESHMUKH
This is a guide for the Indian pharmacist to follow ethics concerning their profession.
It is prepared by pharmacy council of India for pharmacist .
This chapter include information regarding
Code of Pharmaceutical Ethics
1. His job
2. His trade
3. His medical profession
4. His profession
5. Pharmacists Oath
Anti-malarial agents include
Introduction
Classification
Sulphonamide and its classification
Mechanism of action of sulphonamide
Co-triomazole, its MOA
MEDICINAL GASES OR INHALANTS IN PHARMACEUTICALSP.N.DESHMUKH
Medicinal gases includes oxygen, carbon dioxide and nitrous oxide.
Each example includes its formula, mol. wt., chemical properties, uses, storage and precaution.
General anesthetics produce reversible loss of sensation and consciousness through different stages: analgesia, excitement, surgical anesthesia, and medullary paralysis. They are administered via inhalation of gases like halothane or intravenously using liquids like thiopental sodium, ketamine hydrochloride, or propofol. Thiopental sodium is a yellowish powder used as a general anesthetic and sedative. Ketamine hydrochloride is a white crystalline powder used as an anesthetic, sedative, and anticonvulsant. Propofol is a light-straw-colored liquid used for induction and maintenance of general anesthesia.
This presentation explain the knowledge about sedative and hypnotics drugs also its physical properties, storage ,uses,dose, brand name and marketed formulations.
Impurity is the undesirable foreign material which may be toxic or non toxic present in the pharmaceutical substance.
Impurity is the substance or the matter which does not form a part of the medicinal or pharmaceutical substance or drugs.
Sources of impurities include
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2. Process used in the manufacturer.
3. Material of the plant.
4. Inadequate storage.
5. Accidental substitutions/deliberate adulteration with spurious/ useless substance.
6. Manufacturing hazards.
This ppt also explain Effects of impurities in pharmacopoeial substance.
This document outlines the basic requirements and functions of a blood centre. It discusses the necessary location, building design, staffing, equipment, supplies, records, and standard operating procedures (SOPs) required. A blood centre must be located away from unsanitary conditions and have a building designed for hygienic blood collection and processing. It needs qualified medical and technical staff, properly maintained equipment, and supplies stored under appropriate conditions. Records of donors, blood/components, and distribution must be kept according to regulations. SOPs must cover all collection, testing, storage, and distribution procedures. The main functions of a blood centre are to recruit and test donors, collect and process blood, store and deliver blood components safely
Introduction to Pharmaceutical ChemistryP.N.DESHMUKH
Introduction to Pharmaceutical Chemistry covers following bits such as
1. Definition
2. Scope
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This document discusses various dental products including cleaning agents, calcium carbonate, anticaries agents, sodium fluoride, dentures, denture adhesives, and mouthwashes. It provides information on their uses, formulations, examples, and storage. Cleaning agents are used to clean teeth and include abrasives like calcium carbonate. Anticaries agents help prevent tooth decay, with fluoride being a commonly used active ingredient. Dentures replace missing teeth. Denture adhesives enhance the hold of dentures. Mouthwashes are antiseptic liquids used to clean the mouth and maintain oral hygiene.
National Pharmaceutical Pricing AuthorityP.N.DESHMUKH
National Pharmaceutical Pricing Authority established by the central government on dated 29 th August 1997 as an independent, autonomous regulator.
Drugs Price Control Order,2013 explained Retail Prices of a scheduled Formulation,Ceiling price of a scheduled formulation,Pharmaceutical
Policy 2002,and National List of Essential Medicines (NLEM).
The poison Act, 1919 was passed on 3rd September , 1919, to control the import, possession and sale of Poisons.
Under the Act, the central Govt. has been authorized to regulate the import of poison across, while the various State Govt. has been authorized to make rules regarding the possession and sale of poison within their respective territories.
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
Why Degree Certificate Attestation is Crucial for Immigration Processes.pdfandrewabshire123
Degree certificate attestation is the process of verifying the authenticity of a degree certificate by relevant authorities to ensure its validity for use in foreign countries for educational or employment purposes.
Union Budget 2024 presented by Nirmala Sitharaman – LIVE.pdfTheBharatWeekly
The Union Budget 2024, presented by Finance Minister Nirmala Sitharaman on July 23, 2024, has garnered significant attention for its focus on infrastructure, income tax reforms, and economic growth. This budget aims to address various sectors, including railways, healthcare, education, and more, with a vision of making India a developed nation by 2047.
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This presentation covers the fundamental principles of taxation law, focusing on the provisions within the Indian Constitution (Articles 264-289) that deal with finance, contracts, and property. It outlines the need for government finance, details the Income Tax Act of 1961, and discusses the distribution of revenues between the union and states. The presentation also delves into the structure of income tax, including its determination, exemptions, deductions, and the categorization of income. Additionally, it explores the residential status for tax purposes and distinguishes between capital and revenue receipts and expenditures.
THE MAHARASHTRA APARTMENT OWNERSHIP ACT, 1970.pdfNitin Chalwadi
The Maharashtra Apartment Ownership Act, 1970, is a landmark legislation designed to regulate apartment ownership in Maharashtra, India. It provides a legal framework to ensure the rights, responsibilities, and protections of apartment owners are clearly defined and upheld.
THE MAHARASHTRA RENT CONTROL ACT, 1999.pdfNitin Chalwadi
Understanding the Maharashtra Rent Control Act, 1999, is essential for both landlords and tenants in Maharashtra. The Act ensures that rental practices are fair, transparent, and regulated, fostering a harmonious relationship between landlords and tenants.
2. To control certain types of the advertisements relating to drugs.
To prohibit certain kinds of advertisements relating to magic
remedies which falsely claim and mislead public.
To provide for matters related therewith.
OBJECTIVE
1
2
3
3. 1. Any notice, circular, label, wrapper or otherwise such document.
2. Any announcement made orally or by means of producing or
transmitting light, sound/smoke.
Advertisements
Magic Remedy
It includes a Talisman, Mantra, Kavacha, and any other charm claiming to
possess miraculous powers:
1. For diagnosis, treatment and prevention of any disease in human beings
or animals, or
2. For affecting or altering the structure or organic function of
the body or animal.
4. It includes
1. A medicine for the internal or external use of human beings
or animals.
2. A substance intended for the diagnosis, cure, mitigation,
treatment or prevention of disease in human or animals
Registered Medical Practitioner
Any person who holds a qualification granted by an authority
specified in ,or notified under, Sec.3 of the Indian medical
Degrees Act,1916 or specified in the schedules to the Indian
Medical Council Act,1956.
Drug
5. Advertisements relating to drugs
Advertisements relating to drugs which are likely to be
used in disease
Advertisements relating to magic remedies
Prohibited advertisements
Banned
6. a. The procurement or miscarriage (abortion) or the prevention of
conception (pregnancy) in women.
b. The correction of menstrual disorders in women.
c. The maintenance or improvement of capacity of human being for
sexual pleasure.
d. Diagnosis, cure, mitigation, treatment or prevention of any
disease / disorder specified in schedule ‘J’of the Act.
schedule ‘J’ disease:
Appendicitis, blindness, cancer, diabetes, kidney stone, paralysis,
etc.
1. Advertisements relating to drugs which are likely to be used in disease
7. i. Which directly / indirectly give false impression
regarding true character of the drug.
ii. Make false claim for it.
iii.Are otherwise false and deceptive.
Claiming their efficacy mentioned in clause(I) by the person
who carries on the profession of administering magic remedies.
2. Advertisements relating to drugs
3. Advertisements relating to magic remedies
8. Exempted advertisements
1. Displayed signboards or notices by the Registered Medical
Practitioner on his premises indicating that the treatment is under
taken for any diseases, disorders or conditions.
2. Drug which is sent confidently in the prescribed manner to
Registered Medical Practitioner.
3. Drugs printed or published by the government or any other
person with prior permission of the government.
4. Book dealing with any matter specified in section 3 for bona fide
scientific or social standpoint.
9. 1. Leaflets or literature accompanying packing of drugs.
2. Advertisements of drugs in medical, pharmaceutical, scientific and
technical journals.
3. Price list published by the licenced manufacturers, importers or distributors
of drugs.
4. Medical literature distributed by medical detailers appointed by the
licenced manufacturers, importers or distributors of drugs.
5. Advertisements of chemical contraceptives for oral use
Various conditions that are not applicable to following classes
10. Offence and penalties
1. Contravention of any of the provision of this Act or rules there under:-
• Punishable with imprisonment up to 6 months or with fine or with both; on first
conviction.
• Punishable with imprisonment up to 1 year or with fine or with both; on
subsequent conviction.
2. In case of contravention by company, every person who, at the time of the
commission of the offences, was in – charge and responsible for the conduct
of company business shall be deemed to be guilty and liable for the
punishment.
However, such person is not liable for punishment if he proves that the offences
was committed his knowledge.
11. Tuberculosis Rheumatism Kidney stone
Leprosy Appendicitis Cataract
Cancer Obesity Heart diseases
Smallpox Blindness Paralysis
Diseases or ailments of which advertisements are prohibited under
DMR(OA)ACT, 1954.OR Mention any 7 diseases or ailments of which
no advertisements should be made to claim their cure as per Drugs
and Magic Remedies(OA)act.