With Veeva Development Cloud, Boehringer Ingelheim aims to accelerate the development of novel medicines.
Boehringer Ingelheim and Veeva Systems announced Boehringer Ingelheim's selection of Veeva Development Cloud to drive end-to-end processes and information sharing.
As part of Veeva Development Cloud, Boehringer Ingelheim will accelerate clinical development with Vault CDMS, Vault CTMS, Vault eTMF, Vault Study Start-up, and Vault Payments, streamline regulatory activities with Vault Registrations, Vault Submissions, Vault Submissions Publishing, and Vault Submissions Archive, and simplify quality processes with Vault QMS and Vault QualityDocs. The company will also start its journey with the Veeva Digital Trials Platform, using Veeva Site Connect to automate information flow with partner research sites.
The transformation is part of Boehringer Ingelheim’s Medicine Excellence initiative that harnesses technology with the aim to build a ‘One Medicine Platform,’ unifying development processes and data in a centralized platform.
Read more about Boehringer Ingelheim’s selection of Veeva Development Cloud here.
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.
Putting Collective Insights Into Action to Advance Cancer Care: Key Examples From ASCO 2025
June 27th 2025At ASCO 2025, clinical operations leaders gained critical insights into how AI tools, bispecific antibodies, and evolving treatment paradigms are reshaping trial design, endpoint selection, and patient stratification.