ActiGraph is now providing scientific services to its clients. These service offerings help clinical trial sponsors maximize the benefits of digital health technologies (DHTs) throughout the clinical development lifecycle.
ActiGraph’s new end-to-end services, which include endpoint design, algorithm validation, biostatistical analysis, and regulatory engagement, are offered in conjunction with the company’s validated, FDA-cleared wearable technology platform. This fit-for-purpose package of solutions is designed to guide study teams through the process of study planning and implementation.
Read more about the new services 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.
FDA Expands Farapulse PFA Approval to Persistent AF After Strong ADVANTAGE AF Trial Results
July 7th 2025Boston Scientific’s Farapulse Pulsed Field Ablation System is now approved for treating persistent atrial fibrillation, following 12-month data from the ADVANTAGE AF trial showing strong safety, high freedom from AF, and no major complications.