Keyword
aXcess™
A Cost-effective IVR/IWR for Clinical Supply Chain Management
Almac’s aXcessTM integrated voice/web response technology empowers clinicians and supply chain professionals to more efficiently manage clinical supplies. A cost-effective alternative to using paper or custom IVR/IWR systems, aXcessTM has been developed with standard functionalities that help keep timelines short and costs low.
By tapping the expertise of supply chain professionals, clinicians, and technologists, Almac’s aXcessTM was designed specifically for managing simple to moderate functional trial requirements. Such trials often do not employ IVR/IWR due to costs and timelines, and that is where aXcessTM fills a large market need. aXcessTM supplies the basic features and functionalities that are necessary for effective supply chain management, at a price point that allows clients to abandon paper-based approaches or spreadsheets.
Key Functions> Patient screening, enrollment, randomisation, and discontinuation Key Features> Integrated phone and web platform |
Key Benefits> Rapid Set-up |
aXcessTM is only available when purchased as part of an integrated services bundle with other Almac supply chain services.
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Almac Advantage
Customer Service
Almac’s customer service is consistently rated one of the highest in the industry by sites and sponsors. Our project teams go above and beyond to ensure that all users’ needs are met throughout the life of a trial.
Experience
Almac has over 20 years of specialised global supply chain management and IVR/IWR experience. Almac’s technology and services have been deployed globally since 1995 in over 80 countries and 60 languages.
Integration
Almac takes a holistic, integrated strategy and approach to packaging, supplies management, and technology. From pre-trial planning to study closeout, Almac manages all of your clinical supply chain needs efficiently.
Technology
Almac’s technology employs a fully redundant, multi-layered secure database and telecommunications network and a user-friendly interface which helps sites and sponsor increase efficiency and productivity in their clinical trials.