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December 2012

 

Clinical courses

Submitted by admin on 28 December 2012

Dear Sir,What is the future prospectus of Pharmaceutical Sales Representative in india because govt distribute free medicines and follow to use Generic medicine in many state like Rajasthan and others also.

 

So,I want to know the future of Pharmaceutical Sales Rep.is secure or not due to this type of activity day by day by govt of india.

Walk in interview for Postgraduation in Pharmacy, Lifesciences for posts of Junior Research Fellow, Research Assistant in National AIDS Research Institute

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Workshop on Applications of Mass & NMR Techniques in Central Drug Research Institute

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Advertisement for Program Coordinator, Project Assistant in Central Drug Research Institute

In order to harness the bioactive principles from the vast marine biota occurring in Indian waters for human therapeutic purposes, Ministry of Earth Sciences, Government of India, has been implementing a multidisciplinary and multi-institutional Research and Development programme on “Development of potential drugs from ocean (Short title : Drugs

Work as Area Business Manager in Sanzyme Ltd

Sanzyme Ltd., is a pharmaceutical manufacturing and marketing company based in Hyderabad for the last 43 years. We are pioneers in manufacturing and Gonodotropins and Probiotics.

Post: Area Business Manager

Institute of Genomics & Integrative Biology (IGIB) invites Project Scientist (Research), Project Scientist (Program Manager)

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INSTRUMENTATION OF ESR SPECTROSCOPY

About Authors:
Lila dhar*1,Surender Jalandra
1Seth G. L. Bihani S. D. College Of Technical Education,
Institute Of Pharmaceutical Sciences & Drug Research,
Gaganpath, Sri Ganganagar, Rajasthan 335001
*ldbudania@gmail.com

ABSTRACT
Electron paramagnetic resonance spectroscopy (EPR) is a powerful tool for investigating paramagnetic species, including organic radicals, inorganic radicals, and triplet states. The basic principles behind EPR are very similar to the more ubiquitous nuclear magnetic resonance spectroscopy (NMR), except that EPR focuses on the interaction of an external magnetic field with the unpaired electron(s) in a molecule, rather than the nuclei of individual atoms. EPR has been used to investigate kinetics, mechanisms, and structures of paramagnetic species and along with general chemistry and physics, has applications in biochemistry, polymer science, and geosciences. The use of cavity stabilised Impatt diode oscillators for ESR spectroscopy is discussed in different experimental conditions: i.e. as microwave sources in reflection cavity homodyne spectrometers, and as marginal oscillators in which the oscillator cavity (a TE011 cylindrical cavity) is the observing cavity. The sensitivity of this second configuration has been theoretically evaluated for the case in which the Impatt itself is used as a detecting element and in which an external detector is used. For each situation the sensitivity has been measured with a DPPH sample at various power levels giving a sensitivity which is comparable with the best commercial units.

VALIDATION OF DRY HEAT STERILIZATION METHODS

About Authors:
Lila dhar*1, Surender Jalandra
1 Seth G. L. Bihani S. D. College Of Technical Education,
Institute Of Pharmaceutical Sciences & Drug Research,
Gaganpath, Sri Ganganagar, Rajasthan 335001
*ldbudania@gmail.com

ABSTRACT
Dry heat is sometimes used for sterilization instead of the much more efficient moist heat because some materials are sensitive to moisture. Dry heat is often used to ensure that glass and other laboratory equipment is free of pyrogenic material. The process of sterilization within a chamber or hot air tunnel is a critical process and there is a regulatory requirement for validation of the process in most countries. Validation is defined as the documented procedure of obtaining, recording and interpreting results to ensure that the dry heat sterilization process has been and will be consistently effective. Dry heat sterilizer validation consists of accurately measuring the temperature at critical points within the sterilization chamber throughout the process. Dry heat process generally employs a temperature between 250°C and 400°C for varying time. The sterilizer is required to heat all parts of its load up to the specified temperature for a specified period long enough to achieve the desired sterility.