| Wednesday, June 27, 2012 | | | | |
Pharm-Olam has offices among the most populated cities in Europe, Latin America, India, South Africa, and the USA to provide cost effective coverage for oncology studies of all sizes. Pharm-Olam has helped bring 2 oncology compounds to NDA approval and have conducted oncology studies in over 30 countries. The majority of our clinical staff are MDs or PhDs, including oncologists in strategic areas for clinical trials. The incidence of oncology indications and standards of treatment can vary widely, so let Pharm-Olam conduct a complimentary feasibility study specific to your protocol and study budgets to use in your resource planning.
Contact us at www.pharm-olam.com, info@pharm-olam.com, USA 1-713-559-7900, UK 44-0-1344-891121. | More Top News | Biotech Laboratory Equipment Auction: June 27 - 28
The Branford Group will auction surplus assets to the continuing growth of Capstone Therapeutics, a major therapeutic peptide developer located in Tempe, Arizona. This biotechnology R&D laboratory's assets will be auctioned electronically on June 27 and 28. Included in this sale is late model biotech and analytical lab instruments and a large consumable supply inventory. Visit The Branford Group's website for more info. Register to Bid!. | | More Featured News | SafeBridge Consultants, Inc. announces two Potent Compound Safety Training offerings (may be taken separately or consecutively)
The SafeBridge original Potent Compound Safety "Boot Camp"® (Boot Camp I) is a comprehensive two-day course in pharmaceutical potent compound safety focused on training EH&S and related professionals in critical technical concepts and proactive safety programs in pharmaceutical industrial hygiene, occupational and environmental toxicology, analytical chemistry, and risk communication.
The SafeBridge Advanced Concepts to Support Drug Development of Potent Compounds from R&D through Manufacturing (Boot Camp II) is a one-day advanced course focused on case studies and problem-solving to address potent compound safety issues in discovery, development, contract manufacturing and commercialization.
COURSE SEATING IS LIMITED AND USUALLY SELLS OUT!
Oct 23 - 25, 2012 Chicago, IL (USA) Nov 6 - 8, 2012 Liverpool, England (UK)
Contact: Susan Custer: susan.custer@safebridge.com or 650-961-4820 x 231 or www.safebridge.com. | | • Southern Pharm (Fort Lauderdale, Florida)
Kelly Scientific Resources Downstream Manager of Purification Manage the development and transfer of Protein purification and protein Bio-Conjugation processes (involving monoclonal antibodies and recombinant proteins) from the client into process development and facilitating its transition into GMP manufacturing.
• Biotech Beach (Santa Monica, California)
Astellas Pharma US Manufacturing Associate I, Cell Culture Complete assigned tasks associated with Cell Culture bioreactor operation. Accurately record process documentation. Assist in troubleshoot equipment or process issues as required. Assist in technical, operational, and documentation problems.
• Rocky Bio (Salt Lake City, Utah)
Watson Pharmaceuticals, Inc. Associate Director, Regulatory Affairs Proprietary Under general direction, functions as primary regulatory contact with regulatory authorities for assigned products and projects. Manages preparation of regulatory submissions, briefing packages and presentations for regulatory agency meetings.
• BioMidwest (Chicago, Illinois)
Takeda Pharmaceuticals Program Manager, GMP Compound Support Leads and manages Quality activities associated with Takeda's pharmaceutical product development programs. This position ensures compliance with applicable regulations and Takeda Quality standards for pharmaceutical operations related to investigational drug product and investigational active pharmaceutical ingredients (API).
• Bio NC (Durham, North Carolina)
Sequenom Inc. Laboratory Associate Perform basic molecular processes associated with laboratory tests such as DNA extraction, PCR, and genomic library preparation under the supervision of certified laboratory personnel.
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BioSpace White Paper Biotech Career Fairs For Job Seekers 101: Control Your Experience By June Salvati, BioSpace Director of Events and Corporate Services | | Helsinn Therapeutics (US) Inc. 1160 US Highway 22, Suite 104 Bridgewater, New Jersey 08807 U.S.A. Phone: 908-203-6549 Fax: 908-231-1459
Helsinn is a privately owned, self-financing pharmaceutical group with headquarters in Lugano, Switzerland and subsidiaries in Ireland and the USA. The Helsinn Group has been built on the basis of a licensing of pharmaceuticals, with the recent addition of medical devices in therapeutic niche areas.
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• Understand the importance of health technology assessment in reimbursement decisions and how to optimize data to get a positive outcome. • Compare different methods that use health economics early in product development and can enable decisions to be made that will reduce R&D costs. • Understand how trials can be designed to provide good evidence to support positive reimbursement decisions.
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Building Novel Applications with Pipeline Pilot to Drive Next Generation Sequencing
This case study shows how scientists are streamlining the process of analyses of DNA sequence information. Enabled by new DNA sequencing technologies, many more scientists and informaticians are interrogating larger and more complex data set.
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