Intralinks Holding, Inc. announced the availability of its electronic investigator-controlled site file (eISF) solution.
Intralinks® Holdings, Inc. , a global SaaS provider of inter-enterprise content management and collaboration solutions, announced the availability of its electronic investigator-controlled site file (eISF) solution, an online document storage tool for investigative sites involved in the clinical trials process. The new solution is designed to improve regulatory compliance and efficiency at the investigator site by offering full control over their investigator site file (ISF). This could positively impact sponsors who must maintain oversight of participant sites by enabling study monitors and inspectors to no longer have to view investigator documents in person.
Read the full release 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.
Gilead Shares Final Data from Phase III MYR301 Trial of Bulevirtide in Chronic Hepatitis Delta Virus
May 7th 2025Long-term results from the study show 90% of patients with chronic HDV who achieved undetectable HDV RNA at 96 weeks of treatment remained undetectable for nearly 2 years post-treatment.