Chiltern Launches Chiltern Safe
Chiltern International Limited , a global contract research organization (CRO), announced the launch of Chiltern SAFE.
Chiltern SAFE is an electronic Tiral Master File solution for clinical trials that facilitates remote management of documents. This helps to save administrative time and increase accuracy and security of records handling. Chiltern SAFE also includes features such as a duplicate document warning system tracking of expected and missing documents as well as electronic submission of documents that do not require original signatures. Chiltern SAFE is fully validated and compliant with 21 CFR part 11 and other regulations.
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.
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.
Funding Cuts Threaten Diversity in Clinical Research
June 27th 2025In this video interview, Kyle McAllister, co-founder, CEO, Trially, discusses how recent federal funding cuts are likely to undermine research focused on underrepresented populations, and why long-term investment in community-based studies is essential to closing persistent health equity gaps.
