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 poison Act, 1919 was passed on 3rd September , 1919, with a view to control the import, possession and sale of Poisons.
It extends to whole of India but is not applicable to the state J&K.
The Act of 1919 replaced the poison Act of 1904.
The term “Poison” has not been defined under the Act.
Under the Act, the central Govt. has been authorised to regulate the import of poison across, while the various State Govt. has been authorised to make rules regarding the possession and sale of poison within their respective territories.
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 poison Act, 1919 was passed on 3rd September , 1919, with a view to control the import, possession and sale of Poisons.
It extends to whole of India but is not applicable to the state J&K.
The Act of 1919 replaced the poison Act of 1904.
The term “Poison” has not been defined under the Act.
Under the Act, the central Govt. has been authorised to regulate the import of poison across, while the various State Govt. has been authorised to make rules regarding the possession and sale of poison within their respective territories.
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.
Drug and magic remedies (objectionable advertisement) act 1954 and rules 1955Dr. Ambekar Abdul Wahid
Definitions, Class of Prohibitions Advertisement - Section 3, Classes of exempted advertisements, Powers of entry, search etc., Offenses and penalties, Scrutiny of misleading advertisements relating to drugs, Manner in which advertisements may be sent confidentially, Case Studies.
Narcotic and Psychotropic Substance act 1985Prakash Mali
The statutory control over narcotic drugs was being exercised under The Opium Act, 1857, The Opium Act, 1878 and The Dangerous Drugs Act, 1930.
India had no legislation regarding narcotics until 1985. Cannabis smoking in India has been known since at least 2000 BC and is first mentioned in the Atharvaveda, which dates back a few hundred years BC.
Drugs and Magic Remedies (Objectionable Advertisements), 1954 Act,1954 Sagar Savale
An Act to control the advertisement of drugs in certain cases, to prohibit the advertisement for certain purposes of remedies alleged to possess magic qualities and to provide for matters connected therewith. This act is not unconstitutional, because it does not interferes with private business and also it does not impose unreasonable restrictions.
National pharmaceutical pricing authority with drugs price control order (dpc...Tushar Morankar
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.
Main Features of the DPCO 2013
• The new order will bring 348 drugs & their 652 formulations under price control.
• The new policy uses a market-based pricing mechanism against the earlier proposed cost-plus method. The ceiling price would be calculated by taking the simple average of prices of all brands of a drug with a market share of 1% or more.
The Prevention of Cruelty to Animals Act, 1960, authored by acclaimed dancer and animal lover, Rukmini Devi Arundale, is an Act of the Parliament of India enacted in 1960 to prevent the infliction of unnecessary pain or suffering on animals and to amend the laws relating to the prevention of cruelty to animals.
This Act was passed in 3rd September , 1919 in India .
To control the possession for sale and the sale whether wholesale or retails , of any specified poison .
Need of poison act ?
The act extends to the whole of India except the state of Jammu and Kashmir where only certain provisions related to the importation of specified poisons into are applicable.
Drug and magic remedies (objectionable advertisement) act 1954 and rules 1955Dr. Ambekar Abdul Wahid
Definitions, Class of Prohibitions Advertisement - Section 3, Classes of exempted advertisements, Powers of entry, search etc., Offenses and penalties, Scrutiny of misleading advertisements relating to drugs, Manner in which advertisements may be sent confidentially, Case Studies.
Narcotic and Psychotropic Substance act 1985Prakash Mali
The statutory control over narcotic drugs was being exercised under The Opium Act, 1857, The Opium Act, 1878 and The Dangerous Drugs Act, 1930.
India had no legislation regarding narcotics until 1985. Cannabis smoking in India has been known since at least 2000 BC and is first mentioned in the Atharvaveda, which dates back a few hundred years BC.
Drugs and Magic Remedies (Objectionable Advertisements), 1954 Act,1954 Sagar Savale
An Act to control the advertisement of drugs in certain cases, to prohibit the advertisement for certain purposes of remedies alleged to possess magic qualities and to provide for matters connected therewith. This act is not unconstitutional, because it does not interferes with private business and also it does not impose unreasonable restrictions.
National pharmaceutical pricing authority with drugs price control order (dpc...Tushar Morankar
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.
Main Features of the DPCO 2013
• The new order will bring 348 drugs & their 652 formulations under price control.
• The new policy uses a market-based pricing mechanism against the earlier proposed cost-plus method. The ceiling price would be calculated by taking the simple average of prices of all brands of a drug with a market share of 1% or more.
The Prevention of Cruelty to Animals Act, 1960, authored by acclaimed dancer and animal lover, Rukmini Devi Arundale, is an Act of the Parliament of India enacted in 1960 to prevent the infliction of unnecessary pain or suffering on animals and to amend the laws relating to the prevention of cruelty to animals.
This Act was passed in 3rd September , 1919 in India .
To control the possession for sale and the sale whether wholesale or retails , of any specified poison .
Need of poison act ?
The act extends to the whole of India except the state of Jammu and Kashmir where only certain provisions related to the importation of specified poisons into are applicable.
this presentation explains about tne history, scope, narcotic drugs and psychotropic substances definitions, offences and penalties, controlled operations, amendments, manufactured drugs, favourable conditions, production, sale of opium.
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.
3. Information and data of preclinical studies.
4. Samples and testing protocols.
5. Prescribing information
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
1. High solubility and High permeability
2. Low solubility and High permeability
3. High solubility and Low permeability
4. Low solubility and Low permeability
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
3. Clinical Development
4.FDA approval
5.Post- Market Safety Monitoring
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
revoke registration, Offences and Penalties.
This PPT covers drug therapy for tuberculosis. It includes classification of antitubercular drugs.
First line agents like Rifampin/Rifampicin
Isoniazide
Pyrazinamide
Ethambutol
Streptomycin
Second line agents
Para amino-salicyclic acid
Kanamycine
Cycloserine
Ethidnamide
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.
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
1. Raw materials used in the manufacturer.
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.
Introduction to Pharmaceutical ChemistryP.N.DESHMUKH
Introduction to Pharmaceutical Chemistry covers following bits such as
1. Definition
2. Scope
3. Objective
4. Accuracy
5. Precision
6. Significant figures
7. Types of error
a) Determine error
b) Indetermine error
Dental products describe idea about Variety of inorganic compounds used in dentistry compounds such as Calcium carbonate, Sodium
fluoride, Denture cleaners, Denture adhesives, Mouth
washes, etc.
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 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
A "File Trademark" is a legal term referring to the registration of a unique symbol, logo, or name used to identify and distinguish products or services. This process provides legal protection, granting exclusive rights to the trademark owner, and helps prevent unauthorized use by competitors.
Visit Now: https://www.tumblr.com/trademark-quick/751620857551634432/ensure-legal-protection-file-your-trademark-with?source=share
How to Obtain Permanent Residency in the NetherlandsBridgeWest.eu
You can rely on our assistance if you are ready to apply for permanent residency. Find out more at: https://immigration-netherlands.com/obtain-a-permanent-residence-permit-in-the-netherlands/.
1. Chapter 7
THE POISON ACT,1919
Prepared & Presented by : Priyanka N. Deshmukh
K.Y.D.S.C.T.’s college of pharmacy, Sakegaon
2. Poisons
Any substance that can cause severe organ damage/death if ingested ,breathed
into the body or absorbed through the skin.
OR
Substance that can cause death or serious illness if you eat it ,drink it, etc.
Examples
Arsenic Oxalic acid
Atropine All oxides of mercury
3. Objective
To regulate and control the import, possession and sale of poisons.
List A List B
Arsenic Oxalic acid
Atropine Zinc chloride
Belladonna Poppies
Digitalis Chloroform
Morphine Carbolic acid
4. Possession for sale and sale of any poison
State Government regulate it.
Rules made by State Government.
Grant of licences for the Possession for sale ,wholesale or retail of any specified
poison and fixing of fees to be charged for licences.
Classes of persons to whom the licences for the possession for sale and sale of
poisons are to be granted.
Maximum quantity of any poison that may be sold to a person.
Maintance of registers for the sale of poisons and inspection of the same.
Safe custody of poisons and the labelling of vessels, coverings or packages.
Inspection and examination of any such poison possessed for sale by any vendor.
5. Import of poisons
Regulate by Central
Government.
Permitted only under the
authority of license issued by the
central government.
Observe the conditions of
license.
Should import them across one
of the defined customs frontiers
and in accordance with the
conditions of the license.
6. Offence and penalties
1. Unlawful(illegal) importation, possession for sale and sale of any poison:
Punishable with imprisonment upto 3 months or fine upto Rs.500/- or both on
first conviction and
imprisonment for 6 months or a fine upto Rs.1000/- or both on any subsequent
conviction.
2. Illegal possession of any poison:
Punishable with imprisonment upto 1 years or a fine upto Rs.1000/- or both.
3. Poisons in connection with the offence, together with the vessels, packages or
coverings is liable for confiscation.
7. Power to issue search warrant
The District Magistrate, the sub Divisional Magistrate, or Commissioner of
police may issue warrant for search of any place, where there is reason to
believe that:
1. Any poison is possessed or sold in contravention of the Act
2. Any poison liable for confiscation is kept.
The person to whom warrant is directed, may enter and search the place,
according to the warrant and code of criminal procedure, 1898
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