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Overview3rd Edition of the book: ""Generic Drugs Formulation Manual: Basic Principles of New Products Development"" is an interesting text for all professionals related to the pharmaceutical industry. It is the cornerstone or starting point for the implementation of a unit or a development deparment in those companies that wish to have this type of process within their industries. Francisco De La Torre Quiñónez, Ecuadorian Chemist and Pharmacist, is a professional with considerable experience in Formula Development, Implementation and Design of Pharmaceutical Validation Strategies, and in Sanitary Registration of Medicines in General. After his Ebook entitled: Oral Pharmaceutical Dosage Solids Formulation Manual (Spanish Edition) (Manual de Formulación de Sólidos Orales), released in 2022. Francisco De La Torre brings us in 2023, this work entitled: ""Generic Drugs Formulation Manual: Basic Principles of New Products Development""; in which he covers not only the development of formulations in oral solid dosage forms, but also brings us formulations of semi-solid, liquid and semi-liquid dosage forms, in what regards to general medicines. As a ""Plus +"" to this work, the author brings us a formula of a natural product developed by him years ago, which has been subjected, tested, and approved to a pharmacological study on animals. Full Product DetailsAuthor: Francisco de Latorre QuiñónezPublisher: Edlt Publications Imprint: Edlt Publications Volume: 3 Dimensions: Width: 21.60cm , Height: 0.40cm , Length: 27.90cm Weight: 0.209kg ISBN: 9798224915286Pages: 80 Publication Date: 15 March 2023 Audience: General/trade , General Format: Paperback Publisher's Status: Active Availability: In stock We have confirmation that this item is in stock with the supplier. It will be ordered in for you and dispatched immediately. Table of ContentsReviewsAuthor InformationQuimico y Farmaceutico con experiencia en Validacióoacute;n Farmaceutica, Formulacion, Desarrollo de Formulas y Productos, Farmacovigilancia y registro sanitario de medicamentos en general. /// Chemist and Pharmacist with experience in Pharmaceutical Validation, Formulation, Development of Formulas and Products, Pharmacovigilance and sanitary registration of medicines in general (Marketing Authorization submission processes) Tab Content 6Author Website:Countries AvailableAll regions |