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  • Opening for MR/MT in Pharmaceutical company producing a wide range of quality, affordable generic and branded formulations

    Pharmaceutical company producing a wide range of quality, affordable generic and branded formulations and APIs for the developed and developing markets of the world.

    Post: MR/MT

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  • Career opportunity for Faculty & Non-faculty posts for Pharma Professionals in Birla Institute of Technology

    Birla Institute of

  • MICROSPHERES: FORMULATION & EVALUATION

    About Authors:
    Piyush Gupta*
    Department of Pharmaceutics,
    Regional College of Pharmacy,
    Jaipur, Rajasthan

    ABSTRACT:-
    The term MICROSPHERE is defined as a spherical particle with size varying from 50nm to 2µm, containing a core substance. Microspheres are, in strict sense, spherical empty particles.However, the terms microspheres and microencapsulationare used synonymously. In addition, some related terms are “beads” are used alternatively. Spheres and spherical particles are also usedfor a large size and rigid morphology. The microspheres are characteristically free flowing powders consisting of proteins orsynthetic polymers, which are biodegradable in nature, andideally having a particle size less than 200 micrometer. Novel Drug Delivery Systems are developed to address the challengesof drug development such as Bioavailability, Permeability & Poor solubility. These demand changes in the conventional use of Excipients, the growth of the Biotechnology industry,including Stem cell therapy,Vaccines & Genetic products, also necessitates different drug delivery requirements, there by demonstrating the acceptance of these excipients by the US food & drug administration or other agencies in the major markets.For materials in which Toxicity is a possible concern, formulators can give information about the excipients regulatory acceptance& allowable amount by consulting with excipients manufactures& toxicology experts.

  • REGULATORY ASPECT OF CAPA IN QUALITY MANAGEMENT SYSTEM

    ABOUT AUTHOR:
    Devesh Sharma
    M.Pharm-DRA
    School of Pharmaceutical Sciences, JNU, Rajasthan

    Trainee, Chemist, Ind-swift labs ltd, Mohali, (punjab)
    devesh.m.pharmdra@gmail.com

    ABSTRACT:
    Corrective and Preventive Action (CAPA)is a concept within Good Manufacturing Practice (GMP). CAPA focuses on the systematic investigation of discrepancies (failures and/or deviations) in an attempt to prevent their recurrence. To ensure that corrective and preventive actions are effective, the systematic investigation of the failure incidence is pivotal in identifying the corrective and preventive actions undertaken. CAPA is part of the overall quality management system.CAPA is of paramount importance to the FDA. According to FDA documents CAPA accounts for 30-50% of FDA-483 forms issued for non compliance.

  • HPTLC INSTRUMENTATION: AN OVERVIEW

    ABOUT AUTHORS:
    Arshad Hala
    Seth G. L. Bihani S. D. College of Technical Education,
    Institute of Pharmaceutical Sciences & Drug Research,
    Gaganpath, Sri Ganganagar, Rajasthan -335001, India

    ABSTRACT:
    HPTLC is one type of planar chromatography and most advanced form of instrumental TLC. Now a day, HPTLC is more useful than TLC and HPLC. Because HPTLC is independent of sample application, chromatogram development, detection, etc. it is not only instrumental TLC but entire concept that include widely standardize methodology based on validated method. It is instrument controlled by software. In this review article, we discussed about which type of instrument used in HPTLC, complete HPTLC methodology, How HPTLC better than TLC.

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  • A REVIEW ARTICLE ON RESEARCH & DEVELOPMENT OF PHARMACEUTICAL MEDICINE WITH SPECIAL EMPHASIS ON PREFORMULATION (A NEED FOR DOSAGE FORM DESIGN)

    About Authors:
    Kapil Sharma*, Priyanka Sharma**
    *M.Pharm, Yaresun Pharmaceutical Pvt Ltd, India
    **M.sc, Yaresun Pharmaceutical Pvt Ltd,
    Rajasthan, India.

    Aim: - To search Pharmaceutical medicine (New, Safe & Effective) to enhance health and benefits of patients & community.

    Trends:-Usually search a pharmaceutical medicine is starting from “Drug Discovery and Drug Development” (D4) or Pharmaceutical R&D.
    D4 is very long, very costly and very complex process, so mostly companies put together D4 plan. Drug Discovery and Drug Development is the treds of searching a Pharmaceutical medicine

  • ADDITIVES USED IN THE FOOD PRODUCTS

    About Authors:
    Amit A. Patel , Dr.Vipin Kukkar, Sanjeev Thacker
    Seth G. L. Bihani S.D. College of Technical Education,
    Institute of Pharmaceutical Sciences and Drug Research,
    Sri Ganganagar, Rajasthan, INDIA.

    ABSTRACT:
    Food additives have been much important in food product manufacturing. Additive” became almost synonymous with “adulteration. Food additives are used in the food product toprovide nutrition,to maintain product quality and freshness, to look good. There are many type of food additives are available in the market like anti-oxidants, preservatives,Emulsifier and stabilizers,Sweetener, etc.The “E” number system, intended to assist as a short code for some of the lengthier chemical names and to indicate common European safety approval.

  • VARIOUS DETECTORS USED IN THE HIGH PERFORMANCE LIQUID CHROMATOGRAPHY WITH COMPARISON OF THEIR SENSITIVITY

    About Authors:
    Patel Amit, Hala Arshad, Beniwal Prashant
    Seth G. L. Bihani S.D. College of Technical Education,
    Institute of Pharmaceutical Sciences and Drug Research,
    Sri Ganganagar, Rajasthan, INDIA

    ABSTRACT:
    The HPLC detectors are used to detect the solute present in the eluent comes from the HPLC column. There are various types of detectors available, but Detector selection in HPLC system is most valuable part in the solute detection. After comparison of all detector, find out which is the best detector for our solute analysis? Then Detector selection was carried out.  Comparisons of all detectors are done on the basis of the sensitivity of the detector for that particular solute.

  • ELECTRONIC TRANSITION IN UV VISIBLE SPECTROSCOPY

    About Authors:
    Tarun Patel , Prof. Dr. Vipin Kukkar, Nilesh Sovasia
    Seth G.L. Bihani S.D. College of Technical Education,
    Institute of Pharmaceutical Sciences and Drug Research,
    Sri Ganganagar, Rajasthan, INDIA

    INTRODUCTION
    When we speak of a molecule as being raised to a higher electronic level we mean that an electron has been changed from one orbital to another orbital of higher energy. This electron can be of any kinds we have encountered –a σelectron, a π electron or an n electron. In Ultraviolet region we are confined only to the excitation of the comparatively loosely held n and πelectrons.2

  • A PRIMER ON QUALITY AND SAFETY OF COSMETICS

    About Author:
    Tarun Patel, Prof. Dr. Vipin Kukkar, Amit Patel

    Seth G.L. Bihani S.D. College of Technical Education,
    Institute of Pharmaceutical Sciences and Drug Research,
    Sri Ganganagar, Rajasthan, INDIA

    ABSTRACT:
    It is a product which is used for improvement of appearance of human body by applying it externally on human body. For better results and minimizing risk of adverse reaction of cosmetic products on human body we have to check out and maintain quality of cosmetic products during its manufacturing.  And  also required some safety parameters for manufacturing of cosmetic products. In this review article we discussed briefly about quality and safety parameters during manufacturing of cosmetic products.

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