ConsortiEX Blog

How a Compounding Management System Ensures Drug Quality and Patient Safety

The quality of the Compounded Sterile Preparation you administer to patients is of the utmost importance. It’s critical that your hospital pharmacy adheres to all state boards of pharmacy and federal regulations, and that you do everything you can to ensure drug quality. A Compounding Management System helps with both.

ConsortiEX Will be Attending ASHP Midyear!

The ConsortiEX family is currently ramping up for the 2019 ASHP Midyear Clinical Meeting, but we want to take a moment to thank all of our customers for their continued partnership on our journey to improve patient outcomes, and in securing the pharmaceutical supply chain. We remain committed to providing health care[...]

ConsortiEX ASHP 2019 Summer Meetings and Exhibition Recap

We would like to thank all attendees of the ASHP Summer Meetings who stopped by to see us. Having the opportunity to discuss our compliance solutions, in-person, is one that we do not take for granted.

ConsortiEX is attending the 2019 ASHP Summer Meetings

ConsortiEX will be shipping up to Boston for this year’s ASHP Summer Meeting. We encourage you to stop at Booth 201 for an in-person look at how you can use our intuitive DQSA Compliance solutions to enhance patient safety, ensure quality control and simplify your compliance needs.

DSCSA Compliance as a Service: T3 Verification

ConsortiEX is proud to announce T3 verification, the newest feature to be added to our DSCSA Compliance as a Service (CaaS) module. The T3 Verification process gives pharmacies maximum visibility to all T3 transactions, both electronic and paper, received by their pharmacy.

FDA Guidance Under Current Good Manufacturing Practice

The FDA released a finalized questions and answers guidance on data integrity compliance. The FDA guidance adheres to requirements under current good manufacturing practice ( cGMP) for drugs and biologics.

In Recent Guidance, FDA aims for Patient Safety at 503B Facilities

The FDA has issued a guidance to 503B facilities regarding Current Good Manufacturing Practice (gCMB)

FDA Issues Guidance on Verification Systems

The FDA recently issued a draft guidance regarding verification* systems in accordance with the Drug Supply Chain Security Act (DSCSA).

Take Control of Patient Safety and Quality Control with InsightRX

Just last week, ConsortiEX proudly announced our new InsightRX Passive Audit Monitoring module.

Address Quality Control, Re-insourcing CSP Production with a Central Fill Model

Today, cost and quality issues surrounding compounded sterile preparations (CSP’s) have nearly every major health system investigating what it takes to re-insource production. Most are looking at a hub and spoke approach, where their central-fill Batch Compounding can support the CSP production needs of all the[...]

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