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Handbook of HPLC HPTLC As per the latest PCI syllabus prescribed for BPharm Semester VII

This book 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,
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ISBN: 9789390709809

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Product Description

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    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.

Additional Information
    Publisher CBS Publishers & Distributors
    Binding Paperback
    Size 28×40/16 (trimmed 173×242mm)
    Year 2021
    Edition 1/e
    Pages 252
    Author Rajesh Kumar Nema | G Yuvaraj
    Subject Pharmacy
    About the Author

    Rajesh Kumar Nema M Pharm, PhD, FICC is currently Principal, Rungta Institute of Pharmaceutical Sciences and Research, Bhilai, Chhattisgarh. He is an eminent professor of pharmaceutical chemistry with more than 32 years of undergraduate and postgraduate teaching experience. He started his career from Bhupal Nobles College of Pharmacy, Udaipur. He has worked as acting Principal, BNPG College of Pharmacy, Udaipur; and Director, SD College of Pharmacy and Vocational Studies, Muzaffarnagar, and Lakshmi Narain College of Pharmacy (RCP), Indore. He was President, APTI Rajasthan Chapter, and is a life member of IPA, APTI, IPGA, ISTE, IHPA. He has guided 12 PhD and over 40 MPharm students. He has over 170 research papers published in international and national journals to his credit and presented papers at various pharmacy conferences. He has authored five textbooks, recommended by RGPV, Bhopal, and contributed several book chapters. He is a reviewer for many scientific journals.


    Yuvaraj G M Pharm, PhD, DSc is Project Director, KMC BioMed Valley City, India, and an independent drug discovery CRO-QA consultant. He is a founder/owner of CDN providing IND, CRAMS, CRO preclinical drug discovery, regulatory consultancy to the industry and has experience in the design and implementation of preclinical, clinical and commercial quality systems. He held senior management positions in various organizations (CROs and pharmaceutical companies). His area of expertise includes quality systems and compliance audits for GLP, GCP, GMP, ISO 9001, ISO 15189, ISO 17025 and ISO 27001. He is an expert in the quality systems for computerized data to requirements of GLP, 21 CFR Part 11, GAMP and PIC/S. He has experience of auditing clinical studies (Phase I to Phase III) in various therapeutic areas like oncology, endocrinology, respiratory, CNS and has conducted audits in different geographical locations in India, Africa, Canada and Europe. He has been awarded as a chartered scientist (CSci) by the Science Council.

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