Part I: Policy and economic issues Part II: Pharmaceutical management Part III: Management support systems Policy and legal framework 1 Toward sustainable access to medicines 2 Historical and institutional perspectives 3 Intellectual property and access to medicines 4 National medicine policy 5 Traditional and complementary medicine policy 6 Pharmaceutical legislation and regulation 7 Pharmaceutical production policy 8 Pharmaceutical supply strategies Financing and sustainability chapter 6 ...
UNIT 6 ORIGIN OF Origin of Pharmaceutical PHARMACEUTICAL Legislation LEGISLATION Structure 6.1 Introduction Objectives 6.2 History of Pharmaceutical Legislation in India Genesis of Modern Medicine and Pharmacy th th Pharmacy in the 19 and Early 20 Centuries in India 6.3 Regulations in the Western Countries Legislations during the British Rule 6.4 Drugs Enquiry Committee 6.5 Genesis of the Drugs Act ...
_________________________________________________________________________________________________ Guidance Notes on Registration of Pharmaceutical Products/Substances Version Feb 2022 Pharmacy and Poisons Board of Hong Kong Guidance Notes on Registration of Pharmaceutical Products/Substances Page 1 Contents 1. Preface ...................................................................................................... 3 2. Pharmaceutical products subject to registration ............................................ 3 3. Pharmaceutical products not subject to registration ...................................... 4 4. Criteria for registration ................................................................................ 5 5. Who should apply ....................................................................................... 5 6. How to apply ............................................................................................. 5 7. Use of materials ...
DEPARTMENT OF H EALTH D R U G OF F ICE DRUG REGISTRATION AND IMPORT/EXPORT CONTROL DIVISION Guidance Notes on Classification of Products as “Pharmaceutical Products” the Pharmacy and Poisons Ordinance (Cap. 138) under Preamble 1. According to the Pharmacy and Poisons Regulations (PPR)(Cap. 138A) a subsidiary legislation of the Pharmacy and Poisons Ordinance (PPO)(Cap. 138) , pharmaceutical products (PP) must be registered with the ...
Performa : Hindu College of Pharmacy Lesson Plan Name of the faculty Mrs. Jyoti Discipline Pharmacy Semester 2nd Year Subject Pharmaceutical Jurisprudence Lesson plan Duration 25 weeks (July 16, 2018 to March 30, 2019) Work Load/ week(In hour) Lecture- 02; Practical- NA Week Theory Practical Lecture Topic Practical Topic st rd st st 1 (July 3 1 Origin of Pharmaceutical legislation in India 1 (Batch ...
BP 702 T (Industrial Pharmacy II) Theory Unit V Indian Regulatory Requirements Central Drugs Standard Control Organization (CDSCO) and state licensing authority: Organization and Responsibilities, Certificate of Pharmaceutical Product (COPP), Regulatory requirements and approval procedures of New drugs. Prepared By- Prof (Dr) Ranjan Kumar Sahoo Professor and Director The Pharmaceutical College Barpali Abbreviations DRA- Drug Regulatory authority CDSCO- Central Drugs Standard Control Organization DCGI - ...
LESSON PLAN Name of Faculty: SAURABH MAAN Discipline: D. Pharmacy nd Semester: 2 Year Diploma Subject: Pharmaceutical Jurisprudence Lesson Plan Duration: 25 Weeks (From August 2017 to April 2018) Work load (Lecture/Practical) per week (in hours): Lectures 02, Practical -N.A. WEEK THEORY PRACTICAL LECTURE TOPIC PRACTICAL TOPIC DAY DAY Origin and nature of Pharmaceutical st 1 legislation in India, its scope and 1 objectives ...
GYANDEEP ACADEMY Mr. Arun Patidar (M.Pharm) Mob: 9826672215, 9644067667, 34 Prakash Nagar Navlakha, Indore Download study material (Notes) www.gyandeepacademy.in Key Notes: Pharmaceutical Jurisprudence (206) D Pharm II Year 1. Pharmaceutical legislation in India Origin : st - 1 chemist shop – 1811 – by Mr. Bathgate – Calcutta - Apothecary shop – 1821 – by Smith Stamstreet - Small chemical factory &ndash ...
mArket wAtch Draconian EssEntial commoDitiEs act unDErgoEs amEnDmEnt introduction the essential commodities Act (ecA), 1955 was enacted with an objective to control the production, supply and distribution of, and trade and commerce in certain goods such as vegetables, pulses, edible oils, sugar, etc., which are treated as essential commodities. the purported aim of this Act is to ensure affordability of essential commodities for the poor ...
FARMACIA, 2019, Vol. 67, 3 https://doi.org/10.31925/farmacia.2019.3.25 ORIGINAL ARTICLE STANDARDS FOR GOOD PHARMACY PRACTICE – A COMPARATIVE ANALYSIS ANDREEA CHERTES, OFELIA CRIAN * Pharmaceutical Legislation and Management, Faculty of Pharmacy, “Iuliu Haieganu” University of Medicine and Pharmacy, 12 Ion Creang Street, 400010, Cluj-Napoca, Romania *corresponding author: ofelia.crisan@umfcluj.ro Manuscript received: March 2017 Abstract The purpose of this paper is ...
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