Generic Drugs Formulation Manual

Basic Principles of New Products Development

Francisco de Latorre Qui��nez

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Paperback

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English

Edlt Publications
10 March 2023

Manufacturing industries; Pharmacy & dispensing; Science: general issues

"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 Qui��nez, 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 Formulaci�n de S�lidos 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."

By: Francisco de Latorre Qui��nez
Imprint: Edlt Publications
Dimensions: Height: 279mm, Width: 216mm, Spine: 4mm
Weight: 209g
ISBN: 9798215567128
Pages: 80
Publication Date: 10 March 2023
Audience: General/trade , ELT Advanced
Format: Paperback
Publisher's Status: Active

Quimico y Farmaceutico con experiencia en Validaci�oacute;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)