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1 introduction. 2 general requirements, quality assurance and accreditation of calibration/testing laboratories. 3 good laboratory practices. 4 analytical procedures and analyst validation. 5 profile of a quality control laboratory for pharmaceutical units. 6 analgesices and antipyretics. 7 alimentary drugs. 8 antibiotics. 9 anti-inflammatory drugs. 10 bronchospasm relaxants(anti-asthma). 11 cardiovascular drugs. 12 expectorants and cough suppressants. 13 eye, ear, nasal, preparations. 14 keratolytics and cleansers. 15 rubefacients. 16 sedatives and tranquillisers. 17 topical antifungal and anti-infective preparations. 18 vitamins, minerals and digestive enzyme preparation.
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Dr.P.D. Sethi obtained his Ph.D. from madras university, Madras, India. He has been pursuning his analytical career since last 30 years. All the books authored by him are on practical application of different analytical techniques for analysis of multi-component drug formulations. these books are the only kind on the subject. while serving as chairman, ayurvedic pharmacopoeia of india, Dr. Sethi was instrumental in adopting TLC for finger-print profiling of medicinal plants for their correct identification. it is often said that library of any analytical laboratory, pharmaceutical institute and pharma industry is incomplete without books authored by Dr. Sethi.
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