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PHARMACEUTICAL INDUSTRY EVENTS CALENDAR

Clinical Trial Supply New England 2018

Clinical Trial Supply New England 2018

7-8 March 2018
Boston, MA, USA

Clinical Trial Supply New England has now reached its 7thbirthday! For the 7th annual Clinical Trial Supply New England 2018 conference, we have speakers who will focus primarily on discussing case studies, drawing from their own experiences to share the highs and lows for you to adopt in your trials. The speaker line up consists of leading professionals, who will be covering unique topics such as:

  • Thinking the Unthinkable: Contingency planning for
    natural disasters
  • Work together: Clinical and operational team partnership
  • Future of technological innovation in the supply chain 
  • Working with controlled substances: An investigation into the possible consequences of working with controlled substances 
  • Fault in the system: Hazards of system to system communication and mitigation of consequences 
phone +44 (0)207 936 6400
email events@arena-international.com
web www.arena-international.com/ctsnewengland/
email Boston, MA, USA
 
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Industry Events

Cell Therapy Manufacturing & Gene Therapy Congress

4-6 December 2018, RAI, Amsterdam

Bringing together 300+ leaders and key influencers from pharma and biotech companies on 4 - 6 December 2018 in Amsterdam, Cell Therapy Manufacturing & Gene Therapy will provide you with the latest advice for transforming innovative research to prosperous cell & gene therapy manufacturing.
More info >>

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White Papers

Advantages of Quantitative NMR for the Determination of Relative Response Factors

Novatia, LLC

Quantitative NMR (qNMR) is a technique that is being applied broadly and at an increasing rate in the field of pharmaceutical analysis (1). This white paper highlights the advantages of using qNMR to determine Relative Response Factors (RRFs) for pharmaceutical impurities detectable by HPLC. A single determination of RRFs using qNMR allows for simple and accurate quantitation of impurities which eliminates the need for preparation, qualification, and storage of reference standards. An example is presented here, which demonstrates quantitation of known impurities that have variable responses to UV-VIS detection, thereby providing a more accurate assessment of impurity levels than UV-VIS response alone.
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News and Press Releases

PCI Announces Expansion of its Industry-Leading Cold Chain Infrastructure with Dedicated Minus 40 degrees C Facility

Philadelphia, USA August 29, 2018 PCI Pharma Services (PCI), a full-service provider of specialist outsourced drug manufacturing, Clinical trial services, and commercial packaging to the global healthcare industry, is pleased to announce the completion of a purpose built -40C storage and distribution facility at its North American Clinical Services Center of Excellence.
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