Parexel and Veeva Partner Aim to Accelerate Clinical Trials
Parexel and Veeva Systems have announced a collaboration to accelerate clinical trials through technology and process innovation. The collaboration combines each company’s experience across thousands of studies worldwide.
As part of the partnership, Parexel is standardizing on Veeva’s suite of clinical operations applications, including Veeva Vault eTMF, Vault CTMS, and Vault Study Startup. Veeva Vault CDMS for clinical data management will also become a standard offering available from Parexel to its customers.
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Unifying Industry to Better Understand GCP Guidance
May 7th 2025In this episode of the Applied Clinical Trials Podcast, David Nickerson, head of clinical quality management at EMD Serono; and Arlene Lee, director of product management, data quality & risk management solutions at Medidata, discuss the newest ICH E6(R3) GCP guidelines as well as how TransCelerate and ACRO have partnered to help stakeholders better acclimate to these guidelines.
FDA to Launch National Priority Voucher Program to Speed Drug Reviews for Critical Therapies
June 18th 2025Under the new initiative, companies may receive a voucher enabling FDA review to be shortened from the standard 10–12 months to just 1–2 months following final application submission if the drug addresses US national health priorities.
