भूमिकाओं द्वारा

LSPedia has been a godsend in ensuring our compliance and efficiency, providing a seamless experience that has greatly enhanced our operational capabilities.

Transitioning to LSPedia has transformed the wholesale distributor's operations. OneScan now enables efficient order processing and high-quality EPCIS data exchange, resolving previous system issues and enhancing DSCSA compliance. This swift and seamless implementation has supported the distributor's commitment to service excellence and business continuity.

"The VA has awarded the DSCSA Solution Provider national contract to LSPedia, and will be utilizing OneScan to streamline and optimize our supply chain processes."

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"After doing multiple demos and attempting to use other vendor software (which I found unuseable), I’ll personally be using LSPedia's solution- they appear to me to be the only vendor with certain functionalities built as of the time of writing, such as connection to the Verification Routing Service (VRS) so that I can quickly conduct verifications of suspect product and clear it without the need for manual verification requests to pharmaceutical manufacturers."

LSPedia has been a godsend in ensuring our compliance and efficiency, providing a seamless experience that has greatly enhanced our operational capabilities.

"We decided to make a change to LSPedia; The response times to our questions and issues has much improved, it’s been a much better experience overall."

My experience with LSPedia has been exceptional, and the customer service has been fantastic. I am confident that LSPedia will continue to provide us with compliance to the regulations set forth by DSCSA.

"After doing multiple demos and attempting to use other vendor software (which I found unuseable), I’ll personally be using LSPedia's solution- they appear to me to be the only vendor with certain functionalities built as of the time of writing, such as connection to the Verification Routing Service (VRS) so that I can quickly conduct verifications of suspect product and clear it without the need for manual verification requests to pharmaceutical manufacturers."