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Outsourcing in Clinical Trials Southeast 2018

Outsourcing in Clinical Trials Southeast 2018

13-14 March 2018
Durham, North Carolina

This year’s Outsourcing in Clinical Trials event builds on last year’s incredibly successful conference which will once again be returning to North Carolina with the aim of supporting trial sponsors and solution providers in the RTP and neighbouring regions, ensuring trials are delivered on time and partnerships are bettered.

Celebrating our 7th year, we are thrilled to invite you to join us for the Annual Outsourcing in Clinical Trials Southeast conference. We will once again be meeting in Cary, NC, to discuss, deliberate and debate the latest operational and outsourcing challenges with regards to clinical trials. Over the course of two days you can expect to catch-up with old colleagues and make new lasting business connections to help drive success in your trials.

At each OCT we create a welcoming networking environment and an educational program packed with the latest case studies, techniques and providers to set your trial apart.

Have you been struggling with choosing, managing, and retaining your CRO? Then this is the place for you. With presentations, multiple panel discussion, a workshop and roundtable discussions covering each stage of your relationship, you won’t be struggling for much longer!

With such a packed out program you can’t afford to miss out. We look forward to meeting you in Cary so make sure to book your place today!

phone +44 (0)207 936 6400
email events@arena-international.com
web bit.ly/2CrKcOB
email Durham, North Carolina
 
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Industry Events

Clinical Operations in Oncology Trials West Coast

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White Papers

Backward Thinking

Development of a generic equivalent to a current marketed pressurized metered dose inhaler (pMDI) product brings immense challenges. Thorough analysis is critical to gain a comprehensive understanding of the physical attributes and pharmaceutical performance of the reference marketed product. Many factors need to be assessed, understood and combined in order to successfully develop a generic pMDI which will meet the regulatory and quality requirements as an equivalent product in the anticipated target market.
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News and Press Releases

3P Biopharmaceuticals renews its “Credit Impôt Recherche” (CIR) by the French Ministry of Higher Education and Research

[Noáin, April 22, 2020] 3P Biopharmaceuticals, a European leading Contract Development and Manufacturing Organization (CDMO) specialized in process development and cGMP manufacturing of biologics, has successfully extended its French CIR certificate for another four-year period: 2020-2024.
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