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.
August 2, 2019
As of December 2016, the International Council for Harmonisation (ICH) adopted the revised E6 guideline, entitled “Integrated Addendum to Good Clinical Practice (GCP).” The new regulations within E6(R2) require the Sponsor to manage their study using a risk-based approach.
July 29, 2019
Veristat is excited to attend and exhibit at PharmaSUG China 2019 for the first time. This event is the premier event of the year for statistical programmers, statisticians, data managers, researchers, and others who analyze data in the life sciences. Meet Veristat at Booth #7!
July 21, 2019
Veristat recently announced the opening of an office in Taipei, Taiwan. Veristat is expanding its operations to support the growing client demand for clinical trial, biostatistics and programming excellence in Asia. We are building a highly-experienced team of statistical programmers and clinical trial professionals in our new Taipei office who fit our core values and culture of partnership, respect, innovation, and agility.
June 5, 2019
Meet Veristat at booth #1713 at the upcoming DIA Annual Meeting.
Did you miss Veristat's recent webinar on How To Ensure A Successful FDA Meeting . You can view the on-demand webinar replay and/or download the webinar presentation now by clicking on the links below:
April 23, 2019
April 23, 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.
April 16, 2019
