How long is a monograph?
Monograph lengths are generally not about number of pages, but about word counts. In the humanities you will find monographs ranging from (and even longer) in length. There is no standard length for monographs unless you are writing for a specific publisher/publication which specifies length.
What are the side effects of monograph?
Adverse effects: Diarrhea, galactorrhoea and gynaecomastia can occur.
What is monograph used for?
A publication that specifies for a drug (or class of related drugs) the kinds and amounts of ingredients it may contain, the conditions and limitations for which it may be offered, directions for use, warnings, and other information that its labeling must contain.
What does a monograph contains?
How is a monograph different from a book?
is that book is a collection of sheets of paper bound together to hinge at one edge, containing printed or written material, pictures, etc while monograph is a scholarly book or a treatise on a single subject or a group of related subjects, usually written by one person.
What is monograph test?
Compendial Testing (Pharmacopeias) Compendial monograph (pharmacopeial) tests are standardized methods and specification testing for pharmaceutical raw materials and finished products.
What is meant by monograph?
A monograph is a specialist work of writing (in contrast to reference works) or exhibition on a single subject or an aspect of a subject, often by a single author or artist, and usually on a scholarly subject. In this context only, books such as novels are considered monographs.
How do you write a monograph?
Develop the Monograph Proposal
- A Statement of the Problem. The problem or area that the monograph will address is
- A Brief Review of the Literature. Persons who have already talked and/or written about my topic include… .
- Proposed Research Methods.
- Results, Discussion and Implications.
What is a BP monograph?
BP monographs are designed for products that are manufactured within the quality framework for medicinal products. When applied within this framework, the identification test (or tests) in the monograph are sufficient to confirm that the drug product contains the drug substance on the label.
What does BP stand for in drugs?
The British Pharmacopoeia (BP) is the national pharmacopoeia of the United Kingdom. It is an annually published collection of quality standards for UK medicinal substances, which is used by individuals and organisations involved in pharmaceutical research, development, manufacture and testing.
What is the difference between IP and BP?
Drugs manufactured in India have to be labelled with the mandatory non-proprietary drug name with the suffix I.P. This is similar to the B.P. suffix for British Pharmacopoeia and the U.S.P. suffix for the United States Pharmacopeia.
What is difference between EP and BP?
The BP contains thousands of monographs and one of our areas of expertise is in finished products, while the EP predominantly focuses on starting materials and active pharmaceutical ingredients.
What is JP in medicine?
About the Japanese Pharmacopoeia (JP) The Japanese Pharmacopoeia (JP) is a book of official pharmaceutical standards in Japan, prepared by the JP secretariat in Pharmaceuticals and Medical Devices Agency (PMDA) and established by the Minister of Health, Labour and Welfare (MHLW).
Why pharmacopoeia is needed?
The role of a modern pharmacopoeia is to furnish quality specifications for active pharmaceutical ingredients (APIs), FPPs and general requirements, e.g. for dosage forms. The existence of such specifications and requirements is necessary for the proper functioning or regulatory control of medicines.
Which is Extra Pharmacopoeia?
Martindale: The Complete Drug Reference is a reference book published by Pharmaceutical Press listing some 6,000 drugs and medicines used throughout the world, including details of over 180,000 proprietary preparations. It was first published in 1883 under the title Martindale: The Extra Pharmacopoeia.
Who invented Pharmacopoeia?
A number of early pharmacopoeia books were written by Persian and Arab physicians. These included The Canon of Medicine of Avicenna in 1025, and works by Ibn Zuhr (Avenzoar) in the 12th century (and printed in 1491), and Ibn Baytar in the 14th century.
What is difference between Pharmacopoeia and monograph?
In a broader sense, pharmacopoeia is a reference work for pharmaceutical drug specifications. Descriptions of preparations are called monographs. A monograph is a paper on a single topic.
What do you mean by pharmacopoeial monograph?
An Overview of USP Monographs. Monographs articulate the quality expectations for a medicine including for its identity, strength, purity, and performance. They also describe the tests to validate that a medicine and its ingredients meet these criteria.
What is a British Pharmacopoeia monograph?
Updated annually, the British Pharmacopoeia (BP) is the only comprehensive collection of authoritative official standards for UK pharmaceutical substances and medicinal products. It includes approximately 4,000 monographs which are legally enforced by the Human Medicines Regulations 2012.
How many types of pharmacopoeia are there?
In addition to USP, there are three other large pharmacopeias in the world, the European Pharmacopoeia (EP), the British Pharmacopoeia (BP), and the Japanese Pharmacopoeia (JP), all of which share the goal of publishing and producing quality standards for pharmaceuticals.
What does the US Pharmacopeia do?
USP’s mission is “to improve global health through public standards and related programs that help ensure the quality, safety, and benefit of medicines and foods.” Standards for an article recognized in a USP compendium are expressed in the article’s monograph, the General Notices, and applicable general chapters (such …
Which is the latest edition of IP?
The eighth edition of the Indian Pharmacopoeia (IP 2018) is published by the Indian Pharmacopoeia Commission (IPC) on behalf of the Government of India, Ministry of Health & Family Welfare.
Who is the father of Indian Pharmacopoeia?
He headed a Drugs Enquiry Committee of 1930–31 which examined the need for imports, control and legislation….
|Ram Nath Chopra|
|Died||13 June 1973 (aged 90) Srinagar, Jammu and Kashmir, India|
|Known for||Father of Indian Pharmacology; Doyen of science and medicine|
Who is father of pharmacy?
William Procter, Jr.
Who is the father of Pharmacy *?
William Procter Jr.
Who is first pharmacist in India?