Aryabhatta College of Pharmacy Affiliated to RUHS, Jaipur Approved by PCI, New Delhi VI Semester Name cen Class ......... Roll No. ..BP601T. MEDICINAL CHEMISTRY - III (Theory) 45 Hours Scope: This subject is designed to impart fundamental knowledge on the structure, chemistry and therapeutic value of drugs. The subject emphasis on modern techniques of rational drug design like quantitative structure activity relationship (QSAR), Prodrug concept, combinatorial chemistry and Computer aided drug design (CADD). The subject also emphasizes on the chemistry, mechanism of action, metabolism, adverse effects, Structure Activity Relationships (SAR), therapeutic uses and synthesis of important drugs. Objectives: Upon completion of the course student shall be able to 1. Understand the importance of drug design and different techniques of drug design. 2. Understand the chemistry of drugs with respect to their biological activity. 3. Know the metabolism, adverse effects and therapeutic value of drugs. 4. Know the importance of SAR of drugs. Course Content: Study of the development of the following classes of drugs, Classification, mechanism of action, uses of drugs mentioned in the course, Structure activity relationship of selective class of drugs as specified in the course and synthesis of drugs superseripted by (*) UNIT -1 10 Hours Antibiotics Historical background, Nomenclature, Stereochemistry, Structure activity relationship, Chemical degradation classification and important products of the following classes. -Lactam antibiotics: Penicillin, Cepholosporins, - Lactamase inhibitors, Monobactams Aminoglycosides: Streptomycin, Neomyvin, Kanamycin, Tetracyclines: — Tetracycline,Oxytetracycline, Chlortetracycline, Minocycline, Doxycycline UNIT -II 10 Hours Antibiotics Historical background, Nomenclature, Stereochemistry, Structure activity relationship, Chemical degradation classification and important products of the following classes. 126Macrolide: Erythromycin Clarithromycin, Azithromycin. ‘Miscellaneous: Chloramphenicol*, Clindamycin. Prodrugs: Basic concepts and application of prodrugs design. Antimalarials: Etiology of malaria. Quinolines: SAR, Quinine sulphate, Chloroquine*, Primaquine phosphate, Pamaquine*, Quinacrine hydrochloride, Mefloquine. Biguanides and dihydro triazines: Cycloguanil pamoate, Proguanil. Miscellaneous: Pyrimethamine, Artesunete, Artemether, Atovoquone. ‘UNIT - OL 10 Hours Anti-tubercular Agents Synthetic anti tubercular agents: Isoniozid*, Ethionamide, Ethambutol, Pyrazinamide, Para amino salicylic acid.* Anti tubercular antibiotics: Rifampicin, Rifabutin, _Cycloserine Streptomycine, Capreomycin sulphate. Urinary tract anti-infective agents Quinolones: SAR of quinolones, Nalidixic Acid,Norfloxacin, Enoxacin, Ciprofloxacin*, Ofloxacin, Lomefloxacin, Sparfloxacin, Gatifloxacin, Moxifloxacin ‘Miscellaneous: Furazolidine, Nitrofurantoin*, Methanamine. Antiviral agents: Amantadine hydrochloride, Rimantadine hydrochloride, Mdoxuridine trifluoride, Acyclovir, Gancyclovir, Zidovudine, Didanosine, Zalcitabine, Lamivudine, Loviride, Delavirding, Ribavirin, Saquinavir, Indinavir, Ritonavir. ‘UNIT -IV 08 Hours Antifungal antibiotics: Amphotericin-B, Nystatin, Natamycin, Griseofulvin. Synthetic Antifungal agents: Clotrimazole, Econazole, Butoconazole, Oxiconazole Tioconozole, Miconazole*, Ketoconazole, Terconazole, Itraconazole, Fluconazole, Naftifine hydrochloride, Tolnaftate*. Anti-protozoal Agents: Metronidazole*, Tinidazole, Omidazole, Diloxanide, Jodoquinol, Pentamidine Isethionate, Atovaquone, Eflornithine. Anthelminties: Diethylcarbamazine citrate*, Thiabendazole, Mebendazole*, Albendazole, Niclosamide, Oxamniquine, Praziquantal, Ivermectin. 127Sulphonamides and Sulfones Historical development, chemistry, classification and SAR of Sulfonamides: Sulphamethizole, Sulfisoxazole, Sulphamethizine, Sulfacetamide*, Sulphapyridine, Sulfamethoxaole*, Sulphadiazine, Mefenide acetate, Sulfasalazine, Folate reductase inhibitors: Trimethoprim*, Cotrimoxazole. Sulfones: Dapsone*. UNIT-V Introduction to Drug Design Various approaches used in drug design, Physicochemical parameters used in quantitative structure activity relationship (QSAR) such as partition coefficient, Hammet’s electronic parameter, Tafts steric parameter and Hansch analysis. Pharmacophore modeling and docking techniques. Combinatorial Chemistry: Concept and applications of combinatorial chemistry: solid phase and solution phase synthesis. 128 07 Hoursae eens BP607P. MEDICINAL CHEMISTRY- III (Practical) 4 Hours / week I Preparation of drugs and intermediates 1 Sulphanilamide 2. T-Hydroxy, 4-methyl coumarin 3° Chlorobutanol 4 Triphenyl imidazole 5 Tolbutamide 6 Hexamine TL Assay of drugs 1 Isonicotinic acid hydrazide 2 Chloroquine 3. Metronidazole 4 Dapsone 5 Chlorpheniramine maleate 6 Benzyl penicillin TIT Preparation of medicinally important compounds or intermediates by Microwave irradiation technique TV Drawing structures and reactions using chem draw® V__ Determination of physicochemical properties such as logP, clogP, MR, Molecular weight, Hydrogen bond donors and acceptors for class of drugs course content using drug design software Drug likeliness screening (Lipinskies ROS) Recommended Books (Latest Editions) Wilson and Giswold’s Organic medicinal and Pharmaceutical Chemistry. Foye’s Principles of Medicinal Chemistry. Burger's Medicinal Chemistry, Vol Ito IV. Introduction to principles of drug design- Smith and Williams. Remington’s Pharmaceutical Sciences. Martindale's extra pharmacopoeia. 129BP602 T. PHARMACOLOGY-III (Theory) 45 Hours Scope: This subject is intended to impart the fundamental knowledge on various aspects (classification, mechanism of action, therapeutic effects, clinical uses, side effects and contraindications) of drugs acting on respiratory and gastrointestinal system, infectious diseases, immuno-pharmacology and in additionemphasis on the principles of toxicology and chronopharmacology. Objectives: Upon completion of this course the student should be able to: 1. understand the mechanism of drug action and its relevance in the treatment of different infectious diseases 2. comprehend the principles of toxicology and treatment of various poisoningsand 3. appreciate correlation of pharmacology with related medical sciences. Course Content: UNIT- 10hours 1. Pharmacology of drugs acting on Respiratory system a, Anti -asthmatic drugs b. Drugs used in the management of COPD ¢. Expectorants and antitussives d. Nasal decongestants e. Respiratory stimulants 2. Pharmacology of drugs acting on the Gastrointestinal Tract a. Antiulcer agents, b. Drugs for constipation and diarrhoea, . Appetite stimulants and suppressants. 4. Digestants and carminatives. ce. Emetics and anti-emetics. UNIT-II 10bours 3. Chemotherapy a. General principles of chemotherapy. b. Sulfonamides and cotrimoxazole. ¢. Antibiotics- Penicillins, cephalosporins, chloramphenicol, macrolides, quinolones and fluoroquinolins, tetracycline and aminoglycosides UNIT-I 10hours 3. Chemotherapy a. Antitubercular agents b. Antileprotic agents 131. Antifungal agents 4. Antiviral drugs [Link] f. Antimalarial drugs g. Antiamoebic agents UNIT-IV O8hours 3. Chemotherapy 1. Urinary tract infections and sexually transmitted diseases. ‘m. Chemotherapy of malignancy. 4, Immunopharmacology a. Immunostimulants b. Immunosuppressant Protein drugs, monoclonal antibodies, target drugs to antigen, biosimilars UNIT-V O7hours 5. Principles of toxicology a. Definition and basic knowledge of acute, subacute and chronic toxicity. b. Definition and basic knowledge of genotoxicity, carcinogenicity, teratogenicity and mutagenicity ¢. General principles of treatment of poisoning d. Clinical symptoms and management of barbiturates, morphine, corganophosphosphorus compound and lead, mercury and arsenic poisoning. 6. Chronopharmacology a. Definition of rhythm and cycles b. Biological clock and their si icance leading to chronotherapy. 132BP 608 P. PHARMACOLOGY-III (Practical) 4Hrs/Week 1. Dose calculation in pharmacological experiments 2. Antiallergic activity by mast cell stabilization assay Study of anti-ulcer activity of a drug using pylorus ligand (SHAY) rat model and NSAIDS induced ulcer model. Study of effect of drugs on gastrointestinal motility Effect of agonist and antagonists on guinea pig ileum Estimation of serum biochemical parameters by using semi- autoanalyser Effect of saline purgative on frog intestine Insulin hypoglycemic effect in rabt 9. Test for pyrogens ( rabbit method) 10. Determination of acute oral toxicity (DSO) of a drug from a given data 11. Determination of acute skin irritation / corrosion of a test substance 12. Determination of acute eye irritation / corrosion of a test substance 13. Calculation of pharmacokinetic parameters from a given data 14, Biostatistics methods in experimental pharmacology student's t test, ANOVA) 15. Biostatistics methods in experimental pharmacology (Chi square test, Wilcoxon Signed Rank test) eNO ye *Experiments are demonstrated by simulated experiments/videos Recommended Books (Latest Editions) 1. __ RangH. P., Dale M. M., Ritter J. M., Flower R. J., Rang and Dale's Pharmacology, Churchil Livingstone Elsevier 2. __ Katzung B. G., Masters S. B., Trevor A. J., Basic and clinical pharmacology, Tata Mc ‘Graw-Hill 3. Goodman and Gilman’s, The Pharmacological Basis of Therapeutics 4. Marry Anne K. K., Lloyd Yee Y., Brian K. A., Robbin LC., Joseph G. B., Wayne A. K., Bradley R.W., Applied Therapeutics, The Clinical use of Drugs. The Point Lippincott Williams & Wilkins 5. __ Mycek MJ, Gelnet S.B and Perper M.M. Lippincout’s Hlustrated Reviews- Pharmacology 6. __K.[Link]. Essentials of Medical Pharmacology, , JAYPEE Brothers Medical Publishers (P) Lid, New Delhi. 7. Sharma H. L., Sharma K. K., Principles of Pharmacology, Paras medical publisher Modem Pharmacology with clinical Applications, by Charles [Link]& Robert, 8 Ghosh MN. Fundamentals of Experimental Pharmacology. Hilton & Company, Kolkata, Kulkami SK. Handbook of experimental pharmacology. VallabhPrakashan, 10. _N.Udupa and P.D. Gupta, Concepts in Chronopharmacology. ~ 133BP 603 T. HERBAL DRUG TECHNOLOGY (Theory) 45 hours Scope: This subject gives the student the knowledge of basic understanding of herbal drug. industry, the quality of raw material, guidelines for quality of herbal drugs, herbal cosmetics, natural sweeteners, nutraceutical etc. The subject also emphasizes on Good Manufacturing Practices (GMP), patenting and regulatory issues of herbal drugs ‘Objectives: Upon completion of this course the student should be able to: 1. understand raw material as source of herbal drugs from cultivation to herbal drug product 2. know the WHO and ICH guidelines for evaluation of herbal drugs 3. know the herbal cosmetics, natural sweeteners, nutraceuticals 4, appreciate patenting of herbal drugs, GMP . Course content: UNIT-1 11 Hours Herbs as raw materials Definition of herb, herbal medicine, herbal medicinal product, herbal drug preparation Source of Herbs Selection, identification and authentication of herbal materials Processing of herbal raw material Biodynamic Agriculture Good agricultural practices in cultivation of medicinal plants including Organic farming. est and Pest management in medicinal plants: Biopesticides/Bioinsecticides. Indian Systems of Medicine 4) Basic principles involved in Ayurveda, Siddha, Unani and Homeopathy b) Preparation and standardization of Ayurvedic formulations viz Aristas and Asawas, Ghutika,Churna, Lehya and Bhasma. UNIT-IL ‘7 Hours Nutraceuticals General aspects, Market, growth, scope and types of products available in the market. Health benefits and role of Nutraceuticals in ailments like Diabetes, CVS diseases, Cancer, Initable bowel syndrome and various Gastro intestinal diseases. Study of following herbs as health food: Alfalfa, Chicory, Ginger, Fenugreek, Garlic, Honey, Amla, Ginseng, Ashwagandha, Spirulina Herbal-Drug and Herb-Food Interactions: General introduction to interaction and classification. Study of following drugs and their possible side effects and interactions: Hypercium, kava-kava, Ginkobiloba, Ginseng, Garlic, Pepper & Ephedra. UNIT-IL 10 Hours Herbal Cosmetics 134‘Sources and description of raw materials of herbal origin used via, fixed oils, waxes, gums colours, perfumes, protective agents, bleaching agents, antioxidants in products such as skin care, hair care and oral hygiene products. Herbal excipients: Herbal Excipients — Significance of substances of natural origin as excipients — colorants, sweeteners, binders, diluents, viscosity builders, disintegrants, flavors & perfumes. ‘Herbal formulations : ‘Conventional herbal formulations like syrups, mixtures and tablets and Novel dosage forms like phytosomes UNIT- IV 10 Hours Evaluation of Drugs WHO & ICH guidelines for the assessment of herbal drugs Stability testing of herbal drugs. Patenting and Regulatory requirements of natural products: a) Definition of the terms: Patent, IPR, Farmers right, Breeder's right, Bioprospecting and Biopiracy +b) Patenting aspects of Traditional Knowledge and Natural Products. Case study of Curcuma & Neem. Regulatory Issues - Regulations in India (ASU DTAB, ASU DCC), Regulation of manufacture of ASU drugs - Schedule Z of Drugs & Cosmetics Act for ASU drugs. UNIT-V 07 Hours General Introduction to Herbal Industry Herbal drugs industry: Present scope and future prospects. A brief account of plant based industries and institutions involved in work on medicinal and aromatic plants in India. ‘Schedule T - Good Manufacturing Practice of Indian systems of medicine ‘Components of GMP (Schedule — T) and its objectives Infrastructural requirements, working space, storage area, machinery and equipments, standard operating procedures, health and hygiene, documentation and records. 135BP 609 P, HERBAL DRUG TECHNOLOGY (Practical) 4 hours/ week To perform preliminary phytochemical screening of crude drugs. Determination of the alcohol content of Asava and Arista Evaluation of excipients of natural origin |. Incorporation of prepared and standardized extract in cosmetic formulations like creams, lotions and shampoos and their evaluation. Incorporation of prepared and standardized extract in formulations like syrups, mixtures ‘and tablets and their evaluation as per Pharmacopoeial requirements. Monograph analysis of herbal drugs from recent Pharmacopoeias Determination of Aldehyde content Determination of Phenol content Determination of total alkaloids ener wane Recommended Books: (Latest Editions) 1, Textbook of Pharmacognosy by Trease & Evans. Textbook of Pharmacognosy by Tyler, Brady & Robber. Pharmacognosy by Kokate, Purohit and Gokhale Essential of Pharmacognosy by [Link] Pharmacognosy & Phytochemistry by V.D-Rangari Pharmacopoeal standards for Ayurvedic Formulation (Council of Research in Indian Medicine & Homeopathy) 7. Mukherjee, P.W. Quality Control of Herbal Drugs: An Approach to Evaluation of Botanicals. Business Horizons Publishers, New Delhi, India, 2002. ave ep 136BP 604 T. BIOPHARMACEUTICS AND PHARMACOKINETICS (Theory) 45 Hours Scope:This subject is designed to impart knowledge and skills of Biopharmaceutics and pharmacokinetics and their applications in pharmaceutical development, design of dose and dosage regimen and in solving the problems arised therein. ‘Objectives: Upon completion of the course student shall be able w: 1. Understand the basic concepts in biopharmaceutics and pharmacokinetics and their significance. 2. Use of plasma dmug concentration-time data to calculate the pharmacokinetic parameters to describe the kinetics of drug absorption, distribution, metabolism, excretion, elimination. 3. To understand the concepts of bioavailability and bioequivalence of drug products and their significance. 4. Understand various pharmacokinetic parameters, their significance & applications. Course Content: UNIT-1 10 Hours Introduction to Biopharmaceutics Absorption; Mechanisms of drug absorption through GIT, factors influencing drug absorption though GIT, absorption of drug from Non per oral extra-vascular routes, Distribution Tissue permeability of drugs, binding of drugs, apparent, volume of drug. distribution, plasma and tissue protein binding of drugs, factors affecting protein-drug binding. Kinetics of protein binding, Clinical significance of protein binding of drugs UNIT- I 10 Hours Elimination: Drug metabolism and basic understanding metabolic pathways renal excretion of drugs, factors affecting renal excretion of drugs, renal clearance, Non renal routes of drug excretion of drugs Bioavailability and Bioequivalence: Definition and Objectives of bioavailability, absolute and relative bioavailability, measurement of bioavailability, in-vitro drug dissolution models, in-vitro-in-vivo correlations, bioequivalence studies, methods to ‘enhance the dissolution rates and bioavailability of poorly soluble drugs. UNIT- 10 Hours Pharmacokinetics: Definition and introduction to Pharmacokinetics, Compartment models, Non compartment models, physiological models, One compartment open ‘model. (a). Intravenous Injection (Bolus) (b). Intravenous infusion and (c) Extra vascular administrations. Pharmacokinetics parameters - Ke /2,Vd,AUC,Ka, Cit and CLe- definitions methods of eliminations, understanding of their significance and ‘application:137 UNIT- IV 08 Hours Multicompartment models: Two compartment open model. IV bolus Kinetics of multiple dosing, steady state drug levels, calculation of loading and ‘mainetnance doses and their significance in clinical settins. UNIT-V (07 Hours Nonlinear Pharmacokinetics: a. Introduction, b. Factors causing Non-linearity. c. Michaelis-menton method of estimating parameters, Explanation with example of drugs. Recommended Books: (Latest Editions) Biopharmaceutics and Clinical Pharmacokinetics by, Milo Gibaldi. Biopharmaceutics and Pharmacokinetics; By Robert F Notari Applied biopharmaceuties and pharmacokinetics, Leon Shargel and Andrew [Link] 4th edition Prentice-Hall Inernational edition. USA 4. Bio pharmaceutics and Pharmacokinetics-A Treatise, By D. M. Brahmankar and Sunil B Jaiswal, Vallabh Prakashan Pitampura, Delhi 5. Pharmacokinetics: By Milo Glbaldi Donald, R. Mercel Dekker Ine. 6. Hand Book of Clinical Pharmacokinetics, By Milo Gibaldi and Laurie Prescott by ADIS Health Science Press. . Biopharmaceutics; By Swarbrick Clinical Pharmacokinetics, Concepts and Applications: By Malcolm Rowland and ‘Thomas, N. Tozen, Lea and Febrger, Philadelphia, 1995. (0. Dissolution, Bioavailability and Bioequivalence, By Abdou H.M, Mack, Publishing [Link] 1989. 11. Biopharmaceutics and Clinical Pharmacokinetics-An introduction 4th edition Revised and expanded by Rebort F Notari Marcel! Dekker Inn, New York and Basel, 1987. 12. Remington's Pharmaceutical Sciences, By Mack Publishing Company, PennsylvniaBP 605 T. PHARMACEUTICAL BIOTECHNOLOGY (Theory) 45 Hours ‘* Biotechnology has a long promise to revolutionize the biological sciences and technology. © Scientific application of biotechnology in the field of genetic engincering, medicine and fermentation technology makes the subject interestins * Biotechnology is leading to new biological revolutions in diagn and cure of diseases, new and cheaper pharmaceutical drugs. * Biotechnology has already produced transgenic crops and animals and the future promises lot more. © Itis basically a research-based subject. Objectives: Upon completion of the subject student shall be able to; 1. Understanding the importance of Immobilized enzymes in Pharmaceutical Industries 2. Genetic engineering applications in relation to production of pharmaceuticals 3. Importance of Monoclonal antibodies in Industries 4. Appreciate the use of microorganisms in fermentation technology prevention Unit I 10 Hours a) Brief introduction to Biotechnology with reference to Pharmaceutical Sciences. b) Enzyme Biotechnology- Methods of enzyme immobilization and applications. ©) Biosensors- Working and applications of biosensors in Pharmaceutical Industries. 4d) Brief introduction to Protein Engineering. ) Use of microbes in industry. Production of Enzymes- General consideration - Amylase, Catalase, Peroxidase, Lipase, Protease, Penicillinase. f) Basic principles of genetic engineering. Unit 1 10 Hours a) Study of cloning vectors, restriction endonucleases and DNA ligase. b) Recombinant DNA technology. Application of genetic engineering in medicine. ©) Application of r DNA technology and genetic engineering in the production of: i) Interferon ii) Vaccines- hepatitis- B iii) Hormones-Insulin, 4) Brief introduction to PCR 139Unit 01 10 Hours ‘Types of immunity- humoral immunity, cellular immunity a) Structure of Immunoglobulins ) Structure and Function of MHC ) Hypersensitivity reactions, Immune stimulation and Immune suppressions. 4d) General method of the preparation of bacterial vaccines, toxoids, viral vaccine, antitoxins, serum-immune blood derivatives and other products relative to immunity. ¢) Storage conditions and stability of official vaccines ) Hybridoma technology- Production, Purification and Applications 8) Blood products and Plasma Substituties. Unit IV 08Hours a) Immuno blotting techniques- ELISA, Western blotting, Souther blotting. b) Genetic organization of Eukaryotes and Prokaryotes ©) Microbial genetics including transformation, transduction, conjugation, plasmids and transposons. 4) Introduction to Microbial biotransformation and applications. €) Mutation: Types of mutation/mutants. Unit ¥ 07 Hours a) Fermentation methods and general requirements, study of media, equipments, sterilization methods, aeration process, stirring. b) Large scale production fermenter design and its various controls. ©) Study of the production of - penicillins, citric acid, Vitamin B12, Glutamic acid, Griseofulvin, 4) Blood Products: Collection, Processing and Storage of whole human blood, dried hhuman plasma, plasma Substituties. Recommended Books (Latest edition): 1. BR. Glick and JJ. Pasternak: Molecular Biotechnology: Principles and Applications of RecombinantDNA: ASM Press Washington D.C. 2. RA Goldshy et. al., : Kuby Immunology. 3. J.W. Goding: Monoclonal Antibodies.BP606TPHARMACEUTICAL QUALITY ASSURANCE (Theory) 45 Hours Scope: This course deals with the various aspects of quality control and quality assurance aspects of pharmaceutical industries. It deals with the important aspects like cGMP, QC tests, documentation, quality certifications and regulatory affairs. Objectives: Upon completion of the course student shall be able to: understand the cGMP aspects in a pharmaceutical industry «© appreciate the importance of documentation + understand the scope of quality certifications applicable to pharmaceutical industries © understand the responsibilities of QA & QC departments Course content: UNIT-1 10 Hours Quality Assurance and Quality Management concepts: Definition and concept of Quality control, Quality assurance and GMP Total Quality Management (TQM): Definition, elements, philosophies ICH Guidelines: purpose, participants, process of harmonization, Brief overview of QSEM, with special emphasis on Q-series guidelines, ICH stability testing guidelines Quality by design (QbD): Definition, overview, elements of QbD program, tools ISO 9000 & 15014000: Overview, Benefits, Elements, steps for registration NABL accreditation : Principles and procedures UNIT - I 10 Hours Organization and personnel: Personnel responsibilities, training, hygiene and personal records. Premises: Design, construction and plant layout, maintenance, sanitation, environmental control, utilities and maintenance of sterile areas, control of contamination. Equipments and raw materials: Equipment selection, purchase specifications, maintenance, purchase specifications and maintenance of stores for raw materials. UNIT - 11 10 Hours Quality Control: Quality control test for containers, rubber closures and secondary packing 141materials. Good Laboratory Practices: General Provisions, Organization and Personnel, Facilities, Equipment, Testing Facilities Operation, Test and Control Articles, Protocol for Conduct of a ‘Nonclinical Laboratory Study, Records and Reports, Disqualification of Testing Facilities UNIT-IV 08 Hours ‘Complaints: Complaints and evaluation of complaints, Handling of return good, recalling and waste disposal Document maintenance in pharmaceutical industry: Batch Formula Record, Master Formula Record, SOP, Quality audit, Quality Review and Quality documentation, Reports and documents, distribution records. UNIT-V 07 Hours Calibration and Validation: — introduction, definition and general principles of calibration, qualification and validation, importance and scope of validation, types of validation, validation master plan, Calibration of pH meter, Qualification of UV-Visible spectrophotometer, General principles of Analytical method Validation. Warehousing: Good warehousing practice, materials management Recommended Books: (Latest Edition) 1. Quality Assurance Guide by organization of Pharmaceutical Products of Indit 2. Good Laboratory Practice Regulations, 2™ Edition, Sandy Weinberg Vol. 69. Quality Assurance of Pharmaceuticals- A compendium of Guide lines and Related materials Vol I WHO Publications. ‘A guide to Total Quality Management- Kushik Maitra and Sedhan K Ghosh How to Practice GMP’s — P P Sharma. 1SO 9000 and Total Quality Management ~ Sadhank G Ghosh ‘The International Pharmacopoeia ~ Vol I, Il, Ill, IV- General Methods of Analysis and Quality specification for Pharmaceutical Substances, Excipients and Dosage forms Good laboratory Practices ~ Marcel Deckker Series ICH guidelines, ISO 9000 and 14000 guidelines Nays ee 142