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Webinar | Leveraging FDA’s Expedited Programs to Accelerate Product Development

August 2, 2019

Webinar Summary

Accelerating the development of therapeutic products intended to treat serious conditions has been an interest of the public, legislators, and the scientific community for many years.  
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2019 ASCO Annual Oncology Meeting |  See Us At Booth #4106

April 23, 2019

Visit the Veristat booth #4106 at 2019 ASCO Annual Meeting taking place on May 31 - June 4, 2019. 

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Outsourcing in Clinical Trials East 2019 | Booth #7

April 23, 2019

Meet Veristat at booth #7 at the upcoming OCT East 2019 event taking place in King of Prussia, PA on May 21-22, 2019

We provide impactful strategies and solutions to meet your outsourcing needs in order to plan and run your next clinical trial, program or regulatory submission project.  

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Outsourcing in Clinical Trials Southeast 2019

March 1, 2019

Meet Veristat at the upcoming OCT Southeast 2019 event taking place in Durham, NC on March 26-27, 2019.

We provide impactful strategies and solutions to meet your outsourcing needs in order to plan and run your next clinical trial, program or regulatory submission project.  

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Outsourcing in Clinical Trials West Coast 2019 |  Booth #13

January 25, 2019

Meet Veristat at booth # 13 at the upcoming OCT West 2019 event taking place in Burlingame, CA on February 12- 13, 2019.

We provide impactful strategies and solutions to meet your outsourcing needs in order to plan and run your next clinical trial, program or regulatory submission project.  

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Meet With Veristat at the ASH Annual Meeting 2018

November 26, 2018

Veristat will attend the upcoming ASH Annual Meeting 2018 taking place in San Diego, California from Dec 1-4, 2018, the premier event in malignant and non-malignant hematology.

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Outsourcing in Clinical Trials Southern California 2018

August 29, 2018

Meet Veristat at booth # 24 at OCT SoCal 2018!    As a full service CRO providing impactful strategies and solutions, Veristat can meet all of your outsourcing needs  to support your next clinical trial, program or regulatory submission project. 

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