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October 2016

 

 

academics

 

Clinical research courses

Faculty Recruitment at L.J. Institute of Pharmacy | 18 posts

L.J. Institute of Pharmacy, commonly referred as LJIP, is a private management institute located in Ahmedabad, Gujarat, India. The institute is approved by All India Council for Technical Education (AICTE) and Pharmacy Council of India (PCI) and is the part of L.J. Group of Institutes managed by Lok Jagruti Kendra (LJK) Trust. The institute is affiliated to Gujarat Technological University (GTU). The institute is approved by Department of Scientific and Industrial Research (DSIR), Ministry of Science and Technology, Govt. of India as Scientific and Industrial Research Organization (SIRO)

Required for Junior Research Fellows in DRDE

Defence Research & Development Establishment (DRDE), Gwalior is a premier life science laboratory under Defence Research & Development Organisation (DRDO). It is engaged in R&D activities on detection, protection and decontamination of chemical and biological agents. DRDE provides excellent opportunity to young and motivated researchers to pursue a research work in chemical and life sciences. The core competence of DRDE includes: synthesis, evaluation and process development for toxicants and antidotes; detection and analysis of chemicals at trace levels; development of sensors for chemical and bioloqlca agents; toxicity studies and safety evaluation of chemicals in vitro and in vivo; recombinant DNA and hybridoma technology for detection and prophylaxis against infectious agents; development of immune-based detection systems and kits for chemical and biological agents; development of vector management systems; bioremediation of organic waste at low temperature.

DRDE, Gwalior invites application from eligible and interested candidates for the selection for JRFs, purely on temporary basis.

Post: Junior Research Fellows (JRF)

Walk in interview at Torrent Pharmaceuticals | Job in QC, QA, Data Integrity & Reliability

Torrent Pharma, the flagship company of Torrent Group, is ranked amongst the top pharma companies of India. It is a dominant player in the therapeutic areas of cardiovascular (CV) and central nervous system (CNS) and has achieved significant presence in gastro-intestinal, diabetology, anti-infective and pain management segments. Torrent Pharma has a strong international presence spanning over 70 countries across five continents with over 1200 product registrations. Today, Torrent Pharma, with its state of the art manufacturing and research facilities and a global presence, is all poised to carve a niche foritselfintheinternationalpharmaarena.lt is well set on an exciting growth phase in all directions.

Post : Manager / Asst. Manager / Executive / Assistant

Swedish Orphan Biovitrum AB (publ) (Sobi) has been granted orphan designation by the European Commission (EC) for the company’s development product candidate SOBI003, a chemically modified human recombinant sulfamidase for the treatment of mucopolysaccharidosis type IIIA (Sanfilippo A syndrome). SOBI003 will be included in the EU Community Register of Orphan Medicinal Products.

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AstraZeneca announced that the US Food and Drug Administration (FDA) has accepted a complete re-submission of a New Drug Application (NDA) for sodium zirconium cyclosilicate (ZS-9), a potential new medicine for the treatment of hyperkalaemia (high potassium level in the blood serum) by ZS Pharma, a wholly-owned subsidiary of AstraZeneca. The FDA has indicated that this is a complete class 2 response.

Teva Pharmaceutical Industries Ltd. announced that the U.S. Food and Drug Administration (FDA) has accepted the resubmission of the New Drug Application (NDA) for SD-809 (deutetrabenazine) for the treatment of chorea associated with Huntington disease (HD). The FDA has assigned a Prescription Drug User Fee Act (PDUFA) goal date of April 3, 2017.

Eli Lilly and Company announced  that the U.S. Food and Drug Administration (FDA) has granted approval of LARTRUVO™ (olaratumab injection, 10 mg/mL), in combination with doxorubicin, for the treatment of adults with soft tissue sarcoma (STS) with a histologic subtype for which an anthracycline-containing regimen is appropriate and which is not amenable to curative treatment with radiotherapy or surgery. LARTRUVO's indication is approved under Accelerated Approval, and is based on data from the Phase 2 portion of the pivotal JGDG trial. Continued approval for this indication may be contingent upon verification and description of clinical benefit in a confirmatory trial.