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PHARMACEUTICAL INDUSTRY EVENTS CALENDAR

Clinical Trial Supply Southeast 2018

2-3 October 2018
Cary, North Carolina

Clinical Trial Supply Southeast will return to Cary, North Carolina for fall 2018. Part of our global series of events, this show will attract the leading biotech and pharma companies from the Southeast region, the event will focus on how companies can adapt their supply chains to fit into the highly regulated world.

Over the course of 2 days attendees will enjoy a host of activities to help them manage supply; from networking with their peers, exploring the latest solutions in the exhibition hall and hearing from some of the industry’s leading case studies.

The 2018 Clinical Trial Supply Southeast conference will assemble leading clinical experts, and provide you with the opportunity to discuss the common challenges biotech companies are currently facing. The 2018 agenda will focus on improving the visibility of your supply chain, budgeting and forecasting, running international trials, sourcing comparators, artificial intelligence and much more! Delegates will leave the event with the latest innovative solutions to enhance their trial supply.

Our comprehensive learning programme will feature a series of presentations, workshops, panel debates and round-tables on how companies can design, forecast and manage their pharma supplies. We’ll gather both big and small pharma and offer transferable lessons to all in the industry.

 
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Industry Events

Nordic Life Science Days 10/12 September 2019

10-12 September 2019, Malmo Sweden

Nordic Life Science Days is the largest Nordic partnering conference for the global Life Science industry. Bringing together the best talents in Life Science, offering amazing networking and partnering opportunities, providing inputs and content on the most recent trends. Nordic Life Science Days attracts leading decision makers from the Life Science sector, not only from biotech, pharma and medtech but also from finances, research, policy and regulatory authorities.
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White Papers

Running Better Trials Taking an Intelligent Monitoring Approach

Bioclinica

When it comes to implementing a risk-based monitoring program, it is not just about reducing monitoring visits and doing less Source Document Verification (SDV). It’s about bringing together your people, a solid process, and the right technology to run a better trial. Success with risk-based monitoring requires the ability to make sense of the thousands, if not millions, of data points captured by multiple disparate sources in a clinical trial. With the sheer volume of data generated on a daily basis comes complexity. How does one make sense of it all? Information overload burdens even the most experienced study teams who struggle to understand which data matters most and what it means.
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News and Press Releases

3P Biopharmaceuticals enters into manufacturing agreement with the Swedish company Affibody

[Noáin, May 27, 2019] 3P Biopharmaceuticals, a leading CDMO specialized in the process development and GMP manufacturing of biologics, has signed a collaboration agreement with the Swedish company Affibody for the process transfer, scale-up and GMP commercial manufacturing of a recombinant protein sole property of Affibody.
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