Clinical Trial Supply New England 2016 9-10 March 2016, Boston, MA

The entire process of a clinical trial is expensive. Errors in the trial process can be costly and can potentially damage the quality and outcome of results, lengthening the trial and adding significant costs.

Ensuring that trials run smoothly without supply problems is an important task that has potential financial ramifications.

The event is specifically tailored to small to medium biotechs within Boston and surrounding areas. It is designed to provide first-hand, case study based information to give attendees the knowledge they need to efficiently combat hurdles within the clinical supply chain.

Learn how to:

  • Use IRTs and outline considerations for use to help exploit its potential
  • Explore approaches to help achieve accurate forecasting to minimise delays
  • Discuss the impact of impending European Annex 6 labelling to ensure strategies are in place for a smooth transition from Annex 13 to Annex 6
  • Highlight global regulation difficulties and incorporate strategies to mitigate strict import regulations

Bringing together professionals across small and large companies, the conference combines the knowledge of small, emerging biotechs and large global pharmaceutical companies through seminars and roundtable discussion.

For two days, learn from large global companies and smaller emerging start-ups and absorb the range of content and interactivity that will be available at this industry networking event.

For the opportunity to attend this event, please register and quote reference code MK-EGMP.

For more information and to view the full programme for the event, please visit

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