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Recent News
As new information becomes available, we will post the information here to our recent news and events list.
Advasur, LLC has been named an RxInsider Top 500 Company in Healthcare Systems Development in 2024. The Pharmacy500 is awarded to 500 pharmacy supply chain businesses and associations that significantly impacted dispensing pharmacies in the U.S. over the past year. More information is available at: https://rxinsider.com/Pharmacy500.php
WASHINGTON – The US Food and Drug Administration (FDA) does not intend to further delay enforcement of requirements for manufacturers’ track and trace verification systems under the Drug Supply Chain Security Act (DSCSA) and expects those systems to be up and running this November, asserted Patrizia Cavazzoni, director of the agency’s Center…
SuiteRx has partnered with Advasur LLC to provide our valued clients, a seamless intelligent Track and Trace Reporting Solution to ensure your dispensary(s) are compliant with the Drug Supply Chain Security Act (DSCSA), current and upcoming mandates. KEY COMPONENTS INCLUDE: Uniformly Validate, Set-Up, and Maintained Suppliers Data Other industry service…
Relationship Will Aid Long-Term Care Pharmacies in Regulatory Compliance SoftWriters, Inc., the industry leader in long-term care (LTC) pharmacy software, is excited to partner with Advasur360, a comprehensive suite of Drug Supply Chain Security Act services. At SoftWriters, our mission is to save lives. We provide software solutions for the…
LYON, France – The results of a major operation to crack down on illicit medicines across 89 countries have been announced today. The annual campaign targets illicit medicines that pose a significant threat to consumer safety, including counterfeit medicines and medicines diverted from legal and regulated supply chains. They also…
FDA is issuing this guidance for immediate implementation in accordance with 21 CFR 10.115(g)(2). Submit one set of either electronic or written comments on this guidance at any time. Submit electronic comments to https://www.regulations.gov. Submit written comments to the Dockets Management Staff (HFA-305), Food and Drug Administration, 5630 Fishers Lane,…