Get GPAT Sample Papers For Free
GPAT 2022 Syllabus has been released by the National Testing Agency. GPAT 2022 Syllabus covers many aspects related to Pharmaceuticals, such as Management, Chemistry, Engineering, Technology, and even legal and regulatory knowledge about the pharmaceutical business.
Candidates who are preparing to take the Graduate Pharmacy Aptitude Test (GPAT) must go through the GPAT syllabus 2022 in detail in order to prepare for the exam effectively. On this page, you will be able to see the subject-wise topics and sub-topics that must be covered as part of the GPAT exam. Another advantage of knowing the syllabus of GPAT 2022 beforehand is that aspirants can make a proper timetable and ensure that they follow it religiously in order to crack the exam.
Basic principles of cell injury and adaptation, Basic mechanism of inflammation and repair, Hypersensitivity, Autoimmunity and diseases of immunity, Neoplastic diseases, Shock, Biological effects of radiation, Protein-calorie malnutrition, vitamins, Obesity and starvation, Pathophysiology of common diseases, Infectious diseases
Biopharmaceutics and Pharmacokinetics
Bio-pharmaceutics, Bio-availability and bio-equivalence, Bio-pharmaceutical statistics
General principles, Different classes of compounds, Protection and deprotection of groups, Aromaticity and aromatic chemistry, Different aromatic classes of compounds, Polycyclic aromatic hydrocarbons, Carbonyl chemistry, Heterocyclic chemistry, Bridged rings, Kinetic and thermodynamic control, Stereochemistry, Carbohydrates, Amino acids and proteins, Organometallic chemistry, Pericyclic reactions
Pharmaceutical impurities, Monographs, Isotopes, Therapeutic classes of drugs, Drug metabolism, Various classes of therapeutic agents, Different classes of therapeutic drugs
Pharmacy profession, Introduction to pharmaceuticals, Introduction to dosage form, Route of administration, ADME, Sources of drug information, Allopathic dosage form, Crude extract, Allergenic extract Ayurvedic system of medicine, Homeopathic system of medicine, Biological products, GMP, Pharmaceutical plant, location, layout Dosage form necessities and additives, Powders, Capsules, Tablets Parenterals – products requiring sterile packaging, Suspensions Emulsions, Suppositories, Semisolids, Liquids, Pharmaceutical aerosols Ophthalmic preparations, Preformulations , Radiopharmaceuticals Stability of formulated products, Kinetic principles and stability testing Prolonged action pharmaceuticals, Novel drug delivery system, Cosmetics, Packaging material, GMP and validation, Pilot plant scale-up techniques
General pharmacology, Pharmacology for peripheral nervous system, Pharmacology of cardiovascular system, Drugs acting on urinary system, Drugs acting on the respiratory system, Pharmacology of central nervous system, Pharmacology of endocrine system, Chemotherapy, Autacoids and their antagonists, Pharmacology of drugs acting on the gastrointestinal tract, Chronopharmacology, Immunopharmacology, Chemotherapy of malignant diseases, Peptides and proteins as mediators, Nitric oxide, Vitamins and minerals, Principles of toxicology
Introductory Pharmacognosy, Classification of crude drugs, Sources of crude drugs, Factors influencing quality of crude drugs, Techniques in microscopy, Introduction to phytoconstituents, Principles of plant classification, Pharmaceutical aids, Animal products, Plant products, Toxic drugs, Enzymes, Natural pesticides and insecticides, Adulteration and evaluation of crude drugs, Quantitative microscopy, Biogenetic pathways, Carbohydrates and lipids, Tannins, Volatile oils, Resinous drugs, Glycocides, Alkaloids, Herbarium, Extraction and isolation techniques, Phytopharmaceuticals, Quality control and standardization of herbal drugs, Herbal formulations, Worldwide trade of crude drugs and volatile drug, Plant biotechnology, Herbal cosmetics, Traditional herbal drugs, Plant-based industries and research institutes in India Patents
Importance of quality control in pharmacy, Acid-base titrations, Non-aqueous titrations, Oxidation-reduction titrations, Precipitation titrations, Complexometric titrations, Gravimetry, Extraction techniques , Potentiometry, Miscellaneous methods of analysis, Calibration General principles of spectroscopy, Ultraviolet-visible spectrometry Spectrofluorimetric, Flame photometry and atomic absorption spectrometry, Infrared spectrometry, Proton nuclear magnetic resonance spectrometry, Mass spectrometry, Polarography, Nephelometry and turbidimetry, Chromatography
Composition and physical states of matter, Colligative properties, Thermodynamics, Chemical equilibria, Phase rule, Refractive index, Solutions, Electrochemistry, Ionic equilibrium, Kinetics
Matter, properties of matter, Micromeritics and powder rheology, Surface and interfacial phenomenon, Viscosity and rheology, Dispersion systems, Complexation, Buffer, Solubility
Cell, Carbohydrates, Proteins, Lipids, Vitamins, Biological oxidations and reductions, Enzymes, Nucleic Acids, Hereditary diseases
Plant cell and tissue culture, Animal cell structure, Fermentation technology and industrial microbiology, Recombinant DNA Technology, Process and applications, Biotechnology-derived products, Proteomics, Formulation of proteins and peptides
Introduction to microbiology, Microscopy and staining technique, Biology of microorganisms, Fungi and viruses, Asceptic technique, Sterilization and disinfection, Microbial spoilage, Immunology and health, Vaccines and sera, Microbial assay
Historical background Drug legislation in India, Code of Ethics for Pharmacists, The Pharmacy Act 1948 (inclusive of recent amendments), Drugs and Cosmetics Act 1940, Rules 1945, including New Drug applications, Narcotic Drugs and Psychotropic Substances Act, and Rules thereunder, Drugs and Magic Remedies (Objectionable Advertisements) Act 1954, Medicinal and Toilet Preparations (Excise Duties) Act 1955, Rules 1976, Medical Termination of Pregnancy Act 1970 and Rules 1975, Prevention of Cruelty to Animals Act 1960, Drug (Price Control) Order, Shops and Establishment Act, Factory Act, Consumer Protection Act, Indian Pharmaceutical Industry- An Overview, Industrial Development and Regulation act 1951, Introduction to Intellectual Property Rights and Indian Patent Act 1970,An Introduction to Standard Institutions and Regulatory Authorities such as BIS, ASTM, ISO, TGA, USFDA, MHRA, ICH, WHO, Minimum Wages Act 1948, Prevention of Food Adulteration Act 1954 and Rules 1955.
Clinical pharmacy and therapeutics
General Principles, preparation, maintenance, analysis of observational records in Clinical Pharmacy, Clinical trials, type and phases of clinical trials, placebo, ethical and regulatory issues including Good clinical practice in clinical trials, Therapeutic drug monitoring, adverse drug reaction (ADR), types of ADR, Mechanism of ADR. Drug interaction, Monitoring and reporting of ADR and its significance, Drug information services, Drug interactions, Drug interaction in pediatric and geriatric patients, drug treatment during pregnancy, lactation and menstruation, Pharmacovigilance, Therapeutic drug monitoring, Nutraceuticals, essential drugs and rational drug usage, Age-related drug therapy: concept of posology, drug therapy for neonates, pediatrics and geriatrics. Drugs used in pregnancy and lactation, Drug therapy in gastrointestinal, hepatic, renal, cardiovascular, and respiratory Disorders, Drug therapy for neurological and psychological disorders, Drug therapy in infections of the respiratory system, urinary system, infective meningitis, TB, HIV, malaria, and filaria. Drug therapy for thyroid and parathyroid disorders, diabetes mellitus, menstrual cycle disorders, menopause, and male sexual dysfunction, Drug therapy for malignant disorders like leukemia, lymphoma, and solid tumors, Drug therapy for rheumatic, eye, and skin disorders.
Introduction to management, Planning, and forecasting, Organization, Research management, Inventory management, Communication, Marketing research, Leadership and motivation, Human resource development, GATT, WTO and TRIPS, Standard institutions and regulatory authorities
Fluid flow, Heat transfer, Evaporation, Distillation, Drying, Size reduction and size separation, Extraction, Mixing, Crystallization, Filtration and centrifugation, Dehumidification and humidity control, Refrigeration and air conditioning, Material of constructions, Automated process control systems, Industrial hazards and safety precautions
Dispensing and Hospital Pharmacy
Introduction to laboratory equipment, weighting methodology, handling of prescriptions, labeling instructions for dispensed products. Preparations based on percolation process. Preparations based on maceration process. Study of difference between marketed and dispensed products of different dosage forms. Posological calculations involved in the calculation of dosage for infants. Enlarging and reducing formula, displacement value. Preparations of formulations involving allegation, alcohol dilution, isotonic solution.
Want to know more about GPAT
Typical response between 24-48 hours
Get personalized response
Free of Cost
Access to community
The exam pattern of GPAT 2022 provides details about the structure and format of the examination, which further helps candidates to understand the exam better and strategize accordingly.
No, except GPAT 2022 admit card, candidates are not allowed to carry anything in the exam hall.
Yes, in GPAT 2022 for a wrong response there is a negative marking. If the candidate answered wrong then it results in deduction of 1 mark in the GPAT exam.
In GPAT 2022 examination, there are a total of 125 objective type questions.
The GPAT 2022 syllabus includes various topics such as physical chemistry, pharmaceutical chemistry, pharmacognosy, organic chemistry, etc. Also, candidates aspiring for GPAT 2022 can refer to best books mentioned in this article above for GPAT 2022 preparation.
The GPAT 2021 syllabus covers many pharmaceutical-related aspects, such as chemistry, engineering, management, technology, and even legal and regulatory knowledge about the pharmaceutical business.