MP Vyapam Drug Inspector Syllabus 2017 MPPEB Exam Pattern Download Previous Year Papers www.vyapam.nic.in

MP Vyapam Drug Inspector Syllabus

Looking for latest syllabus for MP Vyapam Exam? If yes then you are one right page…. Here we are providing complete MP Vyapam Drug Inspector Syllabus. Applying aspirants who are preparing for MPPEB Exam may check important topics and plan their exam strategy accordingly. Along with MPPEB Syllabus we are also providing MP Vyapam Exam Pattern. Contenders may download Madhya Pradesh Vyapam Drug Inspector Syllabus in PDF format by visiting the official web portal of organization that is www.vyapam.nic.in by following some simple steps as framed at the beneath section of this page. We are advised to those candidates who want to crack this exam easily with good score that you should practice previous year papers. It helps to understand the level of question which will be asked in the MP Vyapam Drug Inspector Exam. Candidates who want to attain MP Vyapam Drug Inspector Syllabus 2017 may scroll down this web page which is well created by the team of indguru.com

MPPEB Exam Syllabus

Madhya Pradesh Professional Examination Board is going to conduct exam for the recruitment of Drug Inspector post. Huge number of job hunters had applied for MP Vyapam Jobs. If you are one of them contenders then you need to know about important topics for MP Vyapam Exam because everybody knows that a huge competition for the Govt Jobs in Madhya Pradesh. So, for the convenience of applicants here on this page we are providing MP Vyapam Drug Inspector Syllabus. You may check topic wise MPPEB Drug Inspector Syllabus as mentioned below:

Syllabus for the recruitment of Drug Inspector

Pharmaceutical Technology
Capsules: Advantages and disadvantages of capsule dosage form, material for production of hard gelatin capsules, size of capsules, method of capsule filling, soft gelatin, capsule shell and capsule content, importance of base absorption and minimum/gm factors in soft capsules , quality control, stability testing and storage of capsule dosage forms. Microencapsulation: Types of microcapsules, importance of microencapsulation in pharmacy, microencapsulation by phase separation, coacervation, multi orifice, spray drying, spray congealing, polymerisation complex emulsion, air suspension technique, coating pan and other techniques, evaluation of micro capsules.
Tablets:
  • Formulation of different types of tablets, granulation, technology on largescale by various techniques, physics of tablets making, different types of tablet compression machinery and the equipments employed, evaluation of tablets.
  • Coating of Tablets : Types of coating, film forming materials, formulation of coating solution, equipments for coating, coating process, evaluation of coated tablets.
  • Stability kinetics and quality assurance. Parenteral Products: (a)Preformulation factors, routes of administration, water for injection, pyrogenicity, non aqueous vehicles, isotonicity and methods of its adjustment
  • Formulation details, containers and closures and selection.
  • Prefilling treatment, washing of containers and closures, preparation of solution and suspensions, Nfilling and closing of ampoules, vials, infusion fluids, lyophillization & preparation of sterile powders, equipment for large scale manufacture and evaluation of parenteral products.
  • Aseptic Techniquessource of contamination and methods of prevention, Design of aseptic area, Laminar flow bench services and maintenance.
  • Sterility testing of pharmaceuticals.

Surgical Products

  • Definition, primary wound dressing, absorbents, surgical cotton, surgical gauzes etc., bandages, adhesive tape, protective cellulosic hemostastics, official dressings, absorbable and nonabsorbable sutures, ligatures and catguts. Medical prosthetics and organ replacement materials.
  • Packaging of Pharmaceutical Products: Packaging components, types, specifications and methods of evaluation, stability aspects of packaging. Packaging equipments, factors influencing choice of containers, legal and other official requirements for containers, package testing.

Liquid Dosages Forms

Introduction, types of additives used in formulations, Vehicles, stabilizers, preservatives, suspending agents, emulsifying agents, solubilizer, colors, flavours and others, manufacturing packaging and evaluation of clear liquids, suspensions and emulsions official in pharmacopoeia.

Semisolid Dosage Forms

Definitions, types, mechanisms of drug penetration, factors influencing penetration, semisolid bases and their selection. General formulation of semisolids, clear gels manufacturing procedure, evaluation and packaging.

Pharmaceutical Analysis

Quality assurance:

  • GLP, TQM, Quality Review and Quality Documentation. Validation/Qualification
  • (DQ/IQ/OQ/PQ) , validation of equipment, validation of analytical procedures.
  • The theoretical aspects, basic instrumentation, elements of interpretation of spectra, and applications of
  • the following analytical techniques should be discussed :
  • Ultraviolet and visible spectrophotometry
  • Fluorimetry.
  • Infrared spectrophotometry.
  • Magnetic Resonance spectroscopy including 13c NMR.
  • Mass Spectrometry.
  • Flame Photometry.
  • Chromatography(TLC,HPLC,HPTLC,GLC, Paper Chromatography,)
  • Atomic Absorption Spectroscopy.

Pharmacology and toxicology

Introduction and general principle of pharmacology and toxicology: Mode of action, drug receptor interaction, drug antagonist, absorption, distribution, metabolism and excretion, rate of administration, Bioavailability, drug dependence and addiction, drug abuse and toxicity, drug adverse reaction, Drug allergy of Central nervous system, Cardiovascular system, Autonomic nervous system, Gastro intestinal system and Respiratory system. Pharmacology of Autocoids, Hormones, Hormone antagonists, chemotherapeutic agents including anticancer drugs. Bioassays, Immuno Pharmacology. Drugs acting on the blood & blood forming organs. Drugs acting on the renal system.

Microbiology

  • Introduction to the scope of microbiology.
  • Classification of microbes and their taxonomy. Actinomycetes, bacteria,
  • rickettsiae, spirochetes and viruses.
  • Identification of Microbes: Stains and types of staining techniques, electron microscopy. Nutrition, cultivation, isolation of bacteria, actinomycetes, fungi, viruses, etc.
  • Microbial genetics and variation.
  • Control of microbes by physical and chemical methods.
  • Disinfection, factors influencing disinfectants, dynamics of disinfection,
  • disinfectants and antiseptics and their evaluation.
  • Sterilization, different methods, validation of sterilization methods & equipments.
  • Sterility testing of all pharmaceutical products.
  • Microbial assays of antibiotics, vitamins & amino acids.

Pharmacognosy

Source, Chemical constituents, uses and adulteration of the following classes of natural drugs, Rauwolfia, Ipecacuanha, Belladona, Cinchona, Cinnamon, Digitalis, Senna, Aloe, Nuxvomica, Opium Alkaloid, Kurchi, Brahmi, Tulsi, Bael and Ephedra.


Glycosides:
Chemistry and biosynthesis of digitoxin, digoxin, hecogenin, sennosides, diosgenin and sarasapogenin.

Alkaloids: Chemistry, biogenesis and pharmacological activity of atropine and related compounds; quinine, reserpine, morphine, papaverine, ephedrine, ergot and vinca alkaloids.

Hospital & Clinical Pharmacy

Introduction to Clinical Pharmacy. Therapeutic Drug Monitoring Concept of Essential Drugs and Rational Drug use. Drug Store Management and Inventory Control:

(a) Organization of drug store, Types of materials stocked, storage conditions

(b) Purchase and Inventory Control principles, purchase procedures, Purchase order, Procurement and stocking.

Drug distribution Systems in Hospitals:

(a) Out-patient dispensing, methods adopted.

(b) Dispensing of drugs to in-patients. Types of drug distribution systems. Charging policy, labeling.

(c) Dispensing of drugs to ambulatory patients.

(d) Dispensing of controlled drugs.

Manufacture of Sterile and Nonsterile Products:

Policy making of manufacturable items, demand and costing, personnel requirements, manufacturing practice,Master formula Card, production control, Manufacturing records.

Records and Reports:

Prescription filling, drug profile, patient medication profile, cases on drug interaction and adverse reactions, idiosyncratic cases etc.

Medicinal Chemistry

Structure, nomenclature, classification, synthesis, SAR and metabolism of the following category of drugs, which are official in Indian Pharmacopoeia and British Pharmacopoeia. Introduction to drug design. Stereochemistry of drug molecules. Hypnotics and Sedatives, Analgesics, NSAIDS, Neuroleptics, Antidepressants, Anxiolytics, Anticonvulsants, Antihistaminics, Local Anaesthetics, Cardio Vascular drugs – Antianginal agents Vasodilators, Adrenergic & Cholinergic drugs, Cardiotonic agents, Diuretics, Antijypertensive drugs, Hypoglycemic agents, Antilipedmic agents, Coagulants, Anticoagulants, Antiplatelet agents.

 

Chemotherapeutic agents – Antibiotics, Antibacterials, Sulphadrugs. Antiproliozoal drugs, Antiviral, Antitubercular, Antimalarial, Anticancer, Antiamoebic drugs. Diagnostic agents. Preparation and storage and uses of official Radiopharmaceuticals, Vitamins and Hormones. Eicosonoids and their application.

Anatomy and physiology

Elementary knowledge of following systems:-Blood, Digestive System , respiratory system, Eye, Ear, Reproduction system and Urinary system.

Pharmaceutical Jurisprudence

  • Briefer view. And elaborate study of the following.
  • Pharmaceutical Ethics
  • Pharmacy Act 1948.
  • Drugs and Cosmetics Act 1940 and Rules 1945.
  • Narcotic Drugs & Psychotropic Substances Act 1985 & Rules.
  • Drugs Price Control Order.
  • Drugs and Magic Remedies (Objectionable Advertisements) Act 1954
  • Prevention of Cruelty to Animals Act 1960.
  • Drugs Patent Act

Biopharmaceutics & Pharmacokinetics

Introduction to Biopharmaceutics and Pharmacokinetics and their role in formulation development and clinical setting..Biopharmaceutics Passage of drugs across biological barrier (passive diffusion, active transport, facilitated diffusion and pinocytosis). Factors influencing absorptionPhysicochemical, physiological and pharmaceutical. Drug distribution in the body, plasma protein binding. Phamacokinetics Significance of plasma drug concentration measurement.

 

Compartment model-Definition and Scope. Pharmacokinetics of drug absorption -Zero order and first order absorption rate constant using Wagner-Nelson and LooReigel man method. Volume of distribution and distribution coefficient. Compartment kinetics -One compartment and two compartment odels.Determination of pharmacokinetic parameters from plasma and urine data after drug administration by intravascular r and o’al route.Curve fitting (method of Residuals), regression procedures. Clearance concept, Mechanism of renal clearance, clearance ratio, determination of renal clearance.Extraction ratio, hepatic clearance, biliary excretion, Extrahepatic circulation.

Non-linear pharmacokinetics with special reference to one compartment model after 1. V drug administration, Michaeles Menten Equation, detection of non-linearity (Saturation mechanism). Clinical Pharmacokinetics Definition and scope . Dosage adjustment in patients with and without renal and hepatic failure. Design of single dose bioequivalence study and relevant statistics. Pharmacokinetic drug interactions and their significance in combination therapy. Bioavailability and bioequivalence Measures of bioavailability, Cmax, t max, and Area Under the Curve (AUe). Design of single dose bioequivalence study and relevant statistics. Review of regulatory requirements for conduction of Bioequiv alent studies.

Pharmaceutical Biotechnology

Genetic Recombination: Transformation, conjugation, transduction, protoplast fusion and gene cloning and their applications. Development of hybrid om a for monoclonal antibodies. Study of drugs produced by biotechnology such as Activase, Humulin, Humatrope, HB etc. Antibiotics: Historical development of antibiotics. Antimicrobial spectrum and methods used for their standardization.

 

Screening of soil for organisms producing antibiotics, fermenter, its design, control of different parameters. Isolation of mutants, factors influencing rate of mutation. Design of fermentation process. Isolation of fermentation products with special reference to penicillins,streptomycins tetracyclines and vitamin B12

 MP Vyapam Drug Inspector Syllabus 2017: Download PDF

MP Vyapam Drug Inspector Exam Pattern

All applying contenders are informed that to grab MP Vyapam Jobs they have to go through Written Examination for Drug Inspector Vacancy. Madhya Pradesh Vyapam Exam consist 200 marks. In MP Vyapam Exam will be divided into seven parts. The questions will be asked from General Knowledge, General Hindi, General English, General Mathematics, Reasoning Ability, Science and Computer Knowledge. Time duration of exam will be 3 hours. Each right answer will carry one mark and there is no negative marking in this exam. For more details about MP Vyapam Exam Pattern you may go through the link as given at the below section of this page. Time Duration of exam will also be divided on the basis as mentioned below:

MP Vyapam Previous Year Papers

All contenders who are going to appear in MP Vyapam Drug Inspector Exam are advised that they can solve previous year paper to know the difficulties of exam. With the help of previous paper you can also increase your question solving speed. For the ease of applicants we are also providing direct link for previous year papers of Drug Inspector. Interested candidates may go through it.

Drug Inspector Previous Year Paper: Get Here

Here we are also providing direct link for old question papers of MP Vyapam Recruitment. Have a Look!!

Old Question Papers: Check Here

Also CheckMP VYAPAM Drug Inspector Recruitment

Important Note

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