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Advanced ability to handle many complex study designs: With many supply chain parameters, attachments, collaboration, and flexibility for future study designs.
Build multiple demand scenarios: Automatically updated demand forecast based on projected or actual data.
Manage medication lists for open and blinded serialized trials: Perform batch allocation and expiry date calculation in supply monitor. Provide information for internal packaging or CMO and external labeling. Ensure efficient shelf-life management.
Visibility of stock beyond the depot level down to the specific site and kit ID level. Ensure import compliance; picking, packing, and repacking based on medication IDs of clinical kits.
You can only subscribe to one edition.
Licensing is based on the total number of clinical trials per year and follows tiered-volume pricing. The price per unit metric decreases for higher volumes of trials.
Metric Definition: One record is equal to one active clinical trial. Clinical trials include both sponsor-initiated and investigator-initiated trials across all phases. Active status of clinical trials includes not yet recruiting, recruiting, active, not recruiting, or enrolling by invitation.