Handbook of HPLC HPTLC aims to serve as a text for pharmacy students and a comprehensive guide for the analysts working in institutions, universities, QC laboratories and industry. It is a ready reckoner and handbook for the academic/industrial research-oriented readership. It focuses on basic ideas, method development, analytical methods validation and trouble shooting in HPLC and HPTLC which explore their applications in analytical laboratory. It strongly emphasises simple graphical methods of data analysis such as control charts which are key-tools in laboratory accreditation. A large part of the book is concerned with instrumentation, design and analysis of laboratory basic experiments. Practical case studies are used throughout to illustrate the ideas in action.
Rajesh Kumar Nema, MPharm, PhD, FICC is currently the Principal of Rungta Institute of Pharmaceutical Sciences, Bhilai, Chhattisgarh. He is an eminent Professor of Pharmaceutical Chemistry with more than 35 years of undergraduate and postgraduate teaching experience. He began his academic career at Bhupal Nobles College of Pharmacy, Udaipur, and has since held several prestigious positions, including Acting Principal at BNPG College of Pharmacy, Udaipur; Director at SD College of Pharmacy and Vocational Studies, Muzaffarnagar; and Director at Lakshmi Narain College of Pharmacy (RCP), Indore.
Dr. Nema has served as President of the APTI Rajasthan Chapter and is a life member of IPA, APTI, IPGA, ISTE, and IHPA. He has guided over 40 MPharm students and 12 PhD scholars. He has to his credit more than 170 research papers published in national and international journals and has presented numerous papers at pharmacy conferences. Additionally, he has authored 15 textbooks, contributed several book chapters, and serves as a reviewer for many reputed scientific journals.
Yuvaraj G, MPharm, PhD, DSc
Dr. Yuvaraj G is Project Director at KMC BioMed Valley City, India, and an independent drug discovery CRO–QA consultant. He is the founder and owner of CDN, providing IND support, CRAMS, CRO preclinical drug discovery services, and regulatory consultancy to the pharmaceutical industry. He has extensive experience in the design and implementation of preclinical, clinical, and commercial quality systems.
He has held senior management positions across various contract research organizations and pharmaceutical companies. His areas of expertise include quality systems development and compliance audits for GLP, GCP, GMP, ISO 9001, ISO 15189, ISO 17025, and ISO 27001. He is also an expert in quality systems for computerized data, aligned with GLP, 21 CFR Part 11, GAMP, and PIC/S requirements.
Dr. Yuvaraj has audited clinical studies (Phase I to Phase III) across therapeutic areas including oncology, endocrinology, respiratory, and CNS disorders, and has conducted audits across India, Africa, Canada, and Europe. He has been awarded the designation of Chartered Scientist (CSci) by the Science Council.
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