New HPLC Analytical Methods Development and Validation for Qualitative and Quantitative Analysis of Active Pharmaceutical Ingredients (API) , And Impurities in Bulk Drug, Formulation and Plasma

New HPLC Analytical Methods Development and Validation for Qualitative and Quantitative Analysis of Active Pharmaceutical Ingredients (API) , And Impurities in Bulk Drug, Formulation and Plasma

Authors: Dr Phani R S Ch,
Publish Date/ Year : January 2025 | Format: Paperback | Genre : Medical Science | Other Book Detail

Pharmaceutical analysis is essential in the process of quality control as well as quality assurance of pharmaceutical chemicals and their formulations. It provides information on the identity, purity, content and stability of starting materials, excipients and active pharmaceutical ingredients (APIs). It also ensures the safety, efficacy and quality of pharmaceutical products used for therapeutic purpose. Analytical methods are intended to establish the identity, purity, physical characteristics and potency of the drugs that we use. Such methods are developed to support drug testing against specifications during manufacturing and quality release operations, as well as during long-term stability studies.
Pages

212 pages
Language

English
Publication date

January 2025
ISBN-13

978-93-6678-384-0




Book Also Available On


Share:

Delivery


Enter pincode for exact delivery dates


Buy Now
Dr Phani R S Ch

Dr Phani R S Ch

Dr. Phani Rajasekhar CH holds a Ph.D. in Chemistry from K L University. With 19 years of research experience in the field of Chemical Sciences, he has made significant contributions to scientific research. He served as the Technical Director (Quality Control and Quality Assurance) at R V Labs in Guntur for 8 years. He has published 12 research articles (indexed in Scopus). Currently, he is employed with the Ministry of Agriculture and Farmers' Welfare, Government of India.