Almac
announces the launch of its new forecasting platform, COMPASS, which has been specifically designed to improve the accuracy and efficiency of the supply inventory process during clinical studies. COMPASS provides benefits to clients by allowing the Supply Chain Manager to proactively direct the entire clinical supply chain, ultimately saving money that is often lost through inaccurate forecasting or overproduction of supplies.
The uncertainty of the global economy is placing unprecedented financial strains on many companies, and an accurate clinical supply forecast can be a determining factor to ensure clinical supply costs remain within budget. COMPASS allows the Supply Chain Manager to produce material forecasts for bulk product, finished goods, and packaging components. Typically a number of forecast scenarios are produced upfront using available data such as patient recruitment projections and protocol information. Clients can then select the most appropriate model to proceed with.
The strength of COMPASS is its ability to update the material forecast throughout the maintenance phase of the trial based on actual patient usage data. This allows the Supply Chain Manager to then review the system outputs and evaluate production and distribution strategies to ensure they are inline with the forecast.
COMPASS will be offered as part of Almac’s Supply Chain Management services at all sites and for customers of all sizes. It will aid in the packaging, labeling, and distribution of trial supplies on a global level. Companies lacking in-house resources to develop material forecasts, as well as those that already have a forecast and simply need it confirmed and managed for the duration of the study, will benefit from COMPASS and the generation of user-friendly reports.
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.