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Overcoming Common QC Testing Challenges in Compounding Pharmacy [WEBINAR]

Each year, millions of medications are custom-made to satisfy the unique requirements of each patient who might not otherwise have access to the proper quantity or concentration of their therapy, or may need an alternate dosage form of a medication.


These compounded drugs are not only unique, but most of them have short beyond use dates (BUDs). These factors paired with changes to United States Pharmacopeia (USP) regulations supporting limiting BUDs even further, make the development of these drugs extremely complex.


In addition  to the pressure of getting medications to patients in a safe and timely manner, compounding pharmacies face added layers of QC challenges compared to their traditional counterparts, such as:

• Lengthy sterility and endotoxin testing times leading to extended production cycles, inventory storage issues, and delays in getting drug

  products to market within BUD timeframes

• Releasing drug products before results are available from critical QC tests such as sterility and bacterial endotoxin tests leading to

  significant risks to patient safety

• Establishing an environmental monitoring (EM) program for the compounding area and implementing a reliable system to track and trend

  EM results to demonstrate microbial control of the site

• Lab personnel shortages resulting in increased human error and data integrity issues


During this webinar we’ll address these challenges and provide modern solutions that can elevate your processes and accelerate your compounded drug release to market.

Charles River

Charles River News & Announcements

In today’s world, quality and compliance are non-negotiable, and yesterday’s standards are no longer sufficient to meet the demands of a constantly evolving landscape. The field of quality control microbiology is undergoing a disruptive revolution to safeguard patient safety, evolving beyond traditional methods to optimize resources, minimize human error, enable sustainable alternatives, and maintain consistent quality standards. Every test, every result, and every data point define the success of life-changing therapies. That’s why we’re leading a new paradigm, one that redefines efficiency, sustainability, and innovation. Let’s rethink the future of microbial quality control, where modern, automated, data-centric, and scalable solutions are the norm, empowering you to stay ahead in a dynamic regulatory and operational landscape.  Together, we are not just preparing for the future. We’re rethinking it. Because every moment matters.

10-rxinsider-staff

Posted by: RXinsider Staff

RXinsider is a multimedia publishing and technology company offering print publications, digital platforms, events, and content creation services to the B2B pharmacy market.

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