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October 2016

 

 

academics

 

Clinical research courses

Clever Culture Systems AG (CCS), the Swiss based joint venture between Australian medical technology company LBT Innovations Limited (ASX: LBT) and Hettich AG (Switzerland) has received clearance of its 510(k) de novo submission to the US Food and Drug Administration (FDA) for APAS® as a Class II medical device.

Novartis announced data from the phase III COMBI-v study demonstrating an overall survival (OS) and a progression-free survival benefit for patients with BRAF V600 mutation-positive advanced melanoma when treated first-line with the combination of Tafinlar (dabrafenib) + Mekinist (trametinib) compared to vemurafenib monotherapy. The results of this study, which was conducted in 704 patients, are being presented at the European Society for Medical Oncology (ESMO) 2016 Congress in Copenhagen.

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Novartis announced updated results from a Phase II study (ASCEND-3), which demonstrated that anaplastic lymphoma kinase-positive (ALK+) non-small cell lung cancer (NSCLC) patients taking Zykadia® (ceritinib) as their first ALK inhibitor (post-chemotherapy) had a median progression-free survival (PFS) of 18.4 months [95% CI: 10.9-26.3; median follow-up time of 25.9 months, as measured by blinded independent review committee (BIRC).Results were presented during an oral session at the Annual European Society for Medical Oncology Congress (ESMO) in Copenhagen.

Nicox S.A. announced that it has received a Complete Response Letter (CRL) from the U.S. Food and Drug Administration (FDA) regarding the New Drug Application (NDA) for AC-170, its novel, proprietary, cetirizine eye drop formulation, for the treatment of ocular itching associated with allergic conjunctivitis.

Recruitment for Study Monitor/Clinical Research Associate in CDSA - Govt. Jobs | Emoluments Up to Rs. 46,000 pm

Clinical Development Services Agency (CDSA) mission is to create, develop, and nurture world-class clinical product development capacity in India.

Post: Study Monitor/Clinical Research Associate

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Working opportunity as Technical Officer (Pharmacist) at world health oraganization

WHO began when our Constitution came into force on 7 April 1948 – a date we now celebrate every year as World Health Day. We are now more than 7000 people working in 150 country offices, in 6 regional offices and at our headquarters in Geneva.

Title:  NPO - Technical Officer ( Pharmacist) - PN377252

Grade: NO-A

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Walk in Interview in QA, QC, Production at Alpha-Pharma | Only experience candidate

Alpha-Pharma is an export oriented generic company incorporated in late 2005. We opened our office in India in 2006 from where we have build our current organization. As a company we are open minded and always open to new opportunities and possibilities. We encourage an open dialog with our employees which continuously brings new aspects and considerations to our organization.

Post : Officer/ Sr. Officer/ Executive / Sr. Executive

Work as Regulatory Writer, Submission Support,& Document Specialist at Pfizer

Founded in 1849, Pfizer is the world's premier biopharmaceutical company taking new approaches to better health. We discover, develop, manufacture and deliver quality, safe and effective prescription medicines to treat and help prevent disease for both people and animals. We also partner with healthcare providers, governments and local communities around the world to expand access to our medicines and to provide better quality health care and health system support. At Pfizer, colleagues in more than 90 countries work every day to help people stay happier and healthier longer and to reduce the human and economic burden of disease worldwide.

Post : Regulatory Writer, Submission Support,& Document Specialist