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Cell and Gene Meeting On The Mesa

August 3, 2020

Meet Veristat at the Virtual event taking place October 12-14, 2020.

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Gene Therapy for Rare Disorders Europe

August 3, 2020

Meet Veristat at the Virtual event taking place 26-28 October 2020.

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Webinar | Minimize Disruption of Your Oncology Trial

June 4, 2020

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As the world begins to relax restrictions, what are the lessons learned that can catapult us into the next innovation in trial operations for good? 
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Webinar | Are you Ready to Begin Planning your IND Submission?

April 13, 2020

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Submitting an Investigational New Drug (IND) application to the US FDA is a significant step in the development of a new drug or biologic product. But, are you ready? 
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DIA 2020 Virtual Meeting ⎪Booth 138

February 19, 2020

Meet Veristat at the Virtual US DIA Annual Meeting 2020  taking place on 14-18 June 2020, Virtual Booth #138

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ASCO Annual Meeting ⎪Booth 25110

February 19, 2020

Meet Veristat at the ASCO 2020, 30 May – 1 June 2020, Booth 25110

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Chief Medical Officer Summit 2020 -Outsourcing Panel Discussion

February 19, 2020

Connect with Veristat at the CMO Summit, 26-27 October, 2020

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Gene Therapy for Rare Disorders 2020 | Booth and Presentation

February 19, 2020

As of 11 March 2020-  This event is being postponed until early 2020 due to Covid-19 Pandemic

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Outsourcing in Clinical Trials West Coast 2020 | Booth #1

February 19, 2020

Meet Veristat at booth #1 at OCT West, 3-4 March 2020 

 

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Webinar | Achieving Balance in Clinical Trial Database Design: Considerations for Enhancing Clinical Trial Efficiency

November 14, 2019

Webinar Summary:

Designing a clinical trial database is a balancing act.  Any clinical program has multiple stakeholders who have both short-term and long-term goals to achieve.   A good database designer must understand the needs and goals of the sponsor and its various functional project team members.   The designer must consider the ease of use for the clinical trial sites who will be entering the trial data, with the needs of the downstream stakeholders in biostatistics, programming, and medical writing.  Additionally, we not only need to consider today’s priorities, we also must understand the overall strategy of the clinical program, especially as it moves forward past the current stage.  

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