• OPPORTUNITY IN GOVERNMENT OF INDIA FOR DRUG CONTROLLER OFFICER

    • March 10, 2018
    • Posted By : Peeyush Jaiswal
    • 0 Comment
    •   167 views

    Established under the Act Of State Government- “The Rajasthan University Of Health Sciences Act, 2005” (Act No. 1 of 2005)”on 25 day February, 2005, the University aims to disseminate and advance knowledge in medicaland health sciences. The University provides academic and research facilities in various streams to the students studying in various Government Colleges (Medical, Dental, Nursing, Pharmacy & Paramedical) and private colleges/institutions affiliated to this University. The University endeavours the process of making itself a leader in world medical education by focusing on the systemic instructions, teaching, training and research activities.

    Rajasthan Government, Medicine & Health department invites applications from pharmacy graduates

    Post: Drug Controller Officer

    No of vacancies: Total 50 posts

    Age Limit: Minimum age should be 21 years and maximum age should be 47 years; Researved categories will get age benefit as per state government rules.

    Essential Qualification:
    1.    A person who has a degree in Pharmacy or Pharmaceutical Sciences or Medicine with specialization in Clinical Pharmacology or Microbiology from a University established in India by Law. as prescribed in Rule 49 of the Drug & Cosmetics Rule 1945.
    2. Candidate should have knowledge of Devanagari hindi

    Application Process:
    Online application filling will start from 20.03.2018 to 09.04.2018 at uni. website: www.rushraj.org

    Last Date to fill application: 09.04.2018

    Method of selection:- Exam

    DCO (DRUG CONTROL OFFICER) EXAM SYLLABUS IN RAJASTHAN

    1.NATURAL PRODUCTS-
    Pharmacogonosy of senna, Digitalis, Cloves, Cinnamon, Rauwolfia, Ergot, Belladonna, Vinca, Ginseng, Opium and Gelatin. Chemical nature of active constituents, Testes and mode of action of these drugs.
    2.PHARMACEUTICS ( Technology of drug delivery system, Biopharmaceutics, Pharmaceutical legislation)
    Technology of drug delivery system
    Manufature, Standards, Labelling, Packaging and storage of dosage forms like tablet, capsules, liquid orals, injectables, topical preparations, blood products and plasma substitutes, sustain release dosage forms and novel drug delivery systems.
    Sterlisation
     Different method of sterlisation and sterility testing of pharmaceuticals.
    Basics of pharmacokinetics and their importance in formulation, Bioavailability, Bioequivalence, Stability studies.
    Drugs and cosmetics Act and Rules, Pharmacy Act, Narcotic and Psychotropic substances Act, Essential commodities Act, Drugs price control order.
    3.PHARMACEUTICAL ANALYSIS-
    Principles and application of absorption spectroscopy, chromatography, potentiometry, comlexometry, nonaqueous titrations with reference to drugs given in I.P. Microbiological assays and biological standardization of antibiotics and vitamins as per I.P.
    4.PHARMACOTHERAPEUTIC AGENTS AND CLINICAL PHARMACOLOGY- 
    Nomenclature, synthesis, uses, mechanism of action, SAR and metabolism of drugs belonging to the following categories which are official in I.P.
    Neuroleptics and tranquilisers, antihypertensives, antiarrhythmics, vasodilators, diuretics, antibiotics, sulphonamides, analgesic and anti-inflammatory drugs, antihistaminics.antineoplastics, antiamoebics, oral contraceptives, antituberculars and antileprotics, antimalarials, insulin and other antidiabetics, corticosteroids, antiulcer and antiasthmatics.
    Clinical aspects of pharmacy and pharmacology, drug interactions, Basic concepts of drug metabolism.
    Evaluation of drugs in human being/ clinical trails.
    Drug therapy in paediatrics, geriatrics and during pregnancy.
    Radioisotopes in medial practice, biological effects of radiation.
    5.MICROBIOLOGY AND BIOTECHNOLOGY-
    Classification,cultivation, isolation, identification and nutritional needs of bacteria, viruses, protozoa and fungi, microbial genetics and variations, Theoretical aspects of immunity, sources and mode of infection, general methods of preparation, standardization, preservation, storage and uses of vaccines, sera and diagnostic agents, Antigen-antibody reaction, Mycobacterium- tuberculosis, leprosy- salmonella, shigella, spirochetes, mycoplasma, diarrhoeal diseases, ELISA, bacteriology of water, milk and food.
    Drug sesitivity testes for bacteria.
    Fermentation technology- production of alcohol, acetic acid, citric acid, penicillin, tetracycline.
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