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Walk in interview for the post of Junior Research Fellow in National Institute of Nutrition | 14 Posts

Eligible candidates are invited to attend a WALK-IN-INTERVIEW at this Institute on 05th November, 2014 at 09.30 A.M. to 10.30 A.M. for filling up of Fourteen (14) Junior Research Fellowships at this Institute.

Post: Junior Research Fellow

No.of post: 14


Applications are invited for Clinical Research, Pharmacovigilance & Medical Writing Programmes: PG & Executive (Advanced) Diploma


Faculty of Clinical Research, IGMPI

(Approved and Certified by Quality Council of India (QCI), Government of India)
(www.igmpiindia.org)


Programmes Offered:

  • Post Graduate Diploma in Clinical Research
  • Executive Diploma in Clinical Research (Advanced)
  • Post Graduate Diploma in Pharmacovigilance
  • Executive Diploma in Pharmacovigilance (Advanced)
  • Post Graduate Diploma in Medical Writing
  • Executive Diploma in Medical Writing (Advanced)

(Part Time and ‘Distance cum e-learning’ modes, Approved and Certified by QCI, Govt of India)

ENQUIRE NOW >>

About IGMPI
Institute of Good Manufacturing Practices India, registered as a non-profit society with Government of India and a member (as a higher/professional education Institute) of Quality Council of India (QCI), Government of India -presents unique, friendly and interactive platform to get rid of all your GMP related glitches.  GMP- is an essential and most dynamic element of industries like pharmaceutical, Biotechnology, cosmetic, Ayurveda, Homeopathy, medical device and food manufacturing. Keeping self-updated with current GMPs thus becomes inevitable to stay abreast with the changing industry needs and practices. With its mission of "Knowledge Dissemination and Human Resources Development in pharma and healthcare Industries", IGMPI is moving hand in hand with technology advances and has gained recognition as stronger and better training & distance learning platform provider for pharma and healthcare professionals and students in the areas of Good Manufacturing Practices, Quality Assurance & Quality Control; Regulatory Affairs, Intellectual Property Rights, Clinical Research, Pharmacovigilance, Nanotechnology Medical Writing, Medical Coding, Drug Discovery and Development, Public Health and Hospital Management, Pharma Marketing and Pharma Product Management. The courses have been structured and designed under the guidance of field experts and thus promise to impart theoretical and practical knowledge about the defined subjects. Based on high standard of quality, the training programmes have been duly approved and certified by Quality Council of India, Government of India.

For counseling by our experts or prospectus, you may call/write on +91 8130924488, +91-11-26652850, 65353339 & info@igmpiindia.org mentioning the name of the course and your phone number.

Programmes Highlights:

  • Get trained and certified by Quality Council of India, Government of India and IGMPI jointly.
  • Pharma, Biotech, Life Sciences, Chemistry, health supplements and alternate healthcare professionals, executives & students may complete these programmes from their own cities and whilst still being in service, business or education.
  • Post Graduate Diploma is 12 months 'duration programme while Executive Diploma is advanced and fast-track programme of 6 months' duration.
  • Practicals along with theoretical knowledge help students in gaining real world exposure.
  • Delhi Government Approved & ISO 9001:2008 certified laboratory facility.
  • A team of experts who are highly qualified, professionally competent and dedicated have been engaged as the faculty.
  • Recorded lectures help the students in their learning process.
  • Comprehensive, dynamic and advanced study material in an international perspective along with case study based approach.
  • A fee concession of 10% is applicable to candidates belonging to SC/ST/Physically handicapped /weaker section for PG Diploma Courses.
  • Placement assistance by a robust placement cell to kindle the flame of talent in the field of Pharmaceutical sciences.
  • Other Programmes offered in Pharma Good Manufacturing Practices, Quality Assurance and Quality Control, Regulatory Affairs, Intellectual Property Rights, Nanotechnology Medical Coding, Drug Discovery and Development, Public Health and Hospital Management, Pharma Marketing, Pharma Product Management
  • In recent months the Institute has witnessed more and more participation from professionals working with global pharmaceutical, healthcare and food giants like Dr. Reddy’s Laboratories, Aurobindo Pharma, Glenmark Generics, Cipla, Wockhardt, Pfizer, Abbott, Medtronic, Foster Corporation, Ipca Laboratories, Calyx, Mother Dairy, Bliss GVS Pharma, Al Rawabi, Almarai, Green Pastures, SeQuent, PepsiCo India, Mankind, Beryl Drugs, Allergy Therapeutics, CFTRI, Ciron, Sun Pharmaceutical, Novartis, GlaxoSmithKline, Ranbaxy, Biocon etc.

For counseling by our experts or prospectus, you may call/write on +91 8130924488, +91-11-26652850, 65353339 & info@igmpiindia.org mentioning the name of the course and your phone number.

ENQUIRE NOW >>


Career opportunity for Pharmacist in My Health Pharmacy | 25 Posts

My Health Pharmacy is a first-of-its-kind pharmacy chain. Its unique value proposition is that it is not just a pharmacy store, but a health partner to its varied customers. Started in 2012, it is currently running with 14 outlets and has big plans of expansion. My Health Pharmacy assures quality health care along with having customer friendly home delivery and counseling services The employees here are the Health Partners, who are qualified and professional pharmacists.

Post: Pharmacist


ROLE OF PRODRUGS IN SOLUBILITY ENHANCEMENT OF DRUGS

ABOUT AUTHORS:
Kalyana Chakravarthi G*, Vijayaraj S, Venugopal A, Naresh Ch, Saritha B
Department of Pharmaceutical Analysis, Sree Vidyanikethan College of Pharmacy,
Tirupati, A.P., India.
kalyanyadav896@gmail.com

ABSTRACT
Solubility is one of the essential parameters to achieve bioavailability of drug in systemic circulation to produce expected therapeutic response.  Nearly 40% of new drug molecules face solubility challenge. Though several techniques like micronization, crystal engineering, hydrotrophy, solid dispersion and so forth were available for solubility enhancement of poorly soluble drugs based on physical and chemical modification, prodrug approach is a vital technique amongst the other. Prodrugs are biologically inactive compound which can be metabolized in the body to produce active drug. It is estimated that currently about 10% of all world-wide approved drugs are prodrugs. This review extensively confers the role of prodrugs and the kind of promoieties used for solubility enhancement.


Career in U.S. Pharmacopeial Convention for the post of Senior Scientist I, Reference Standards Evaluation

The U.S. Pharmacopeial Convention (USP) is a scientific nonprofit organization that sets standards for the identity, strength, quality, and purity of medicines, food ingredients, and dietary supplements manufactured, distributed and consumed worldwide. USP’s drug standards are enforceable in the United States by the Food and Drug Administration, and these standards are used in more than 140 countries.

Post: Senior Scientist I, Reference Standards Evaluation


Walk in interview for Medical Coding Process in Elico Healthcare

Backed by Elico Limited, with an enviable reputation of five decades of pioneering achievements, stability and business excellence as a manufacturer of laboratory analytical instruments, Elico Healthcare Services is providing back office healthcare processing support for its business partners, and fine tuning the medical billing workflow and processes for over ten years.
Elico has great customer references and a fine team of both management and billing experts who constantly strive to deliver strategic value for our clients, in addition to significant time and cost reductions. We process over one million claims per year, offering our clients savings of up to 30%. Our clients profit from our high degree of accuracy, Turn Around times and reduced denials of over 85%. Net collection rates have gone up significantly by over 95%.

Post: Medical Coding Process


Vacancy as Senior Quality Specialist, RRC in Parexel

PAREXEL has supported the Bio-Tech and Pharmaceutical industries in helping the development of new drugs and treatments on a global basis. As a leading global biopharmaceutical service provider, they supply knowledge-based contract research, medical communications and consulting services across a broad range of therapeutic areas to the worldwide pharmaceutical, biotechnology and medical device industries. They have helped over 800 clients to develop and launch some of the most important drugs and devices of our time-helping people live better and healthier lives everywhere in the world. Headquartered near Boston, Massachusetts, PAREXEL operates in more than 50 countries around the world.

Post: Senior Quality Specialist, RRC


Royal Society of Chemistry (London) - Deccan Section National Symposium on Advances in Pharmaceutical Research at RIPER

ROYAL SOCIETY OF CHEMISTRY (LONDON) – DECCAN SECTION
NATIONAL SYMPOSIUM
ADVANCES IN PHARMACEUTICAL RESEARCH
On
15th November 2014
In Association with
RAGHAVENDRA
INSTITUTE OF PHARMACEUTICAL EDUCATION AND RESEARCH
Granted 12 (b) & 2 (f) status by UGC & NBA Accredited Institution (UG)


Required for M.Pharm as Senior Scientist in Novartis

A global healthcare leader, Novartis has one of the most exciting product pipelines in the industry today. A pipeline of innovative medicines brought to life by diverse, talented and performance driven people. All of which makes them one of the most rewarding employers in their field.

Post: Senior Scientist


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