Compliant facilities.
All facilities supplying Vier products comply with applicable cGMP and FDA requirements and relevant ISO standards. Facility and product documentation can be discussed as part of your qualification process.
QUALITY & VISIBILITY
From manufacturing requirements to batch information, we help define the details behind your healthcare product program.
All facilities supplying Vier products comply with applicable cGMP and FDA requirements and relevant ISO standards. Facility and product documentation can be discussed as part of your qualification process.
Vier offers sterile product capability. Each program defines its formulation, substrate, packaging, sterility status and labeling. The agreed product specification and validated shelf life govern the final configuration.
Discuss the documentation your program requires, including approved specifications, certificates of analysis or conformance, and applicable sterility or microbial-quality records.
Batch-level traceability connects your program to its product lots. Lot identification, manufacturing and expiration information, and shipment documentation are addressed within the agreed program scope.
THE VIER DASHBOARD · NOW LIVE
The Vier customer dashboard is now live, bringing orders, purchased batches and planning information into one place. Buyers are using these insights to reduce costs and make more informed purchasing decisions.
Explore order history and purchased batch details, including quantities, lot references, manufacturing dates and expiration dates.
View recorded stock, consumption trends and purchase mix. Planning views explore days of supply, projected runout and reorder gaps from recorded inputs.
Review chronological quality updates connected to an order and batch, with actions, follow-up dates and recorded outcomes.
Available to Vier customers. Email our team for access or a guided walkthrough. Planning projections depend on recorded inputs and assumptions.
Request a walkthrough by emailOur longer-term vision includes broader document access, expiration exposure and recall analysis as the platform develops.
LET’S TALK