PRO Consulting® announced that it has expanded its line of Patient Reported Outcomes (PRO) services to support new biopharmaceutical and medical device developers as they implement PROs throughout all stages of their clinical development programs.
While many of the services offered by PRO Consulting are customized to meet individual client needs, developers of biopharmaceutical and medical device products are already benefiting from the expanded portfolio of strategic and tactical services offered by PRO Consulting. Services now being offered include:
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.