ARL Bio Pharma is a high-quality laboratory who partners
with compounding pharmacies and outsourcing facilities. 
February News and Updates
ARL Bio Pharma is excited to introduce the Quality Compounding Summit taking place in Oklahoma City, Oklahoma, September 8-9, 2017. This educational conference is in partnership with American College of Apothecaries. Save the date and join us as we elevate excellence within the compounding industry! Speakers include: Joe Cabaleiro, Gates Healthcare Associates; Dr. Loyd Allen, International Journal of Pharmaceutical Compounding; Tony J. Park, Pharm.D., J.D., California Pharmacy Lawyers; Dr. Thomas C. Kupiec, ARL Bio Pharma; and, a board of pharmacy guest speaker.

For more information and to register visit: https://qcsummitrx.org/  


New ARL Price List
Click here to view ARL 2017 Price List.

ARL Bio Pharma values our partnership with pharmacists bringing excellence to the compounding industry. Effective March 1, 2017, ARL is implementing new pricing for microbiology testing. New prices include a microbial identification price reduction, the addition of antibiotic microbiology test pricing, and a new tier for sterility pricing of large volume parenterals.   
Click here to view Amended Q_A document.
Extending Beyond Use Dating Webinar Q&A

In December 2016, ARL hosted a webinar "Extending Beyond Use Dating of Compounded Preparations". Our laboratory received several questions during the webinar and provided answers during the Q&A session. 

To view webinar recording, click here and register. The recording will appear upon registration and login.

This live online continuing education is offered at no cost to our clients. Participants must view the entire presentation, and complete the course evaluation to receive continuing education credit.

A Stability Indicating Method (SIM) is defined as a validated analytical procedure that accurately and precisely measures active ingredients (drug substance or drug product) free from process impurities, excipients and degradation products. SIMs must be validated for the specific formulation being tested. The stability indicating method is used to perform the assay (test) and ultimately extend the beyond use date.

This session will illustrate how stability indicating methods are performed and include specific examples for quantitative assays.  A comparison of stability indicating methods and release methods will be presented for sterile and non-sterile products.  Participants will gather an understanding of the basic process for developing and validating stability indicating Assays.

Participants will learn to:
  • Define a stability indicating method.
  • Explain how a stability indicating method is different than a release (or potency) method.
  • Describe the process for developing and validating a stability indicating assay method. 
 

 
Look for ARL at these upcoming events:
Educational Conference, February 22-25, 2017, in San Diego, California
Western Pharmacy  Exchange, February 23-25, 2017 in Palm Springs, California
  ARL Bio Pharma | (800) 393-1595 | info@arlok.com | www.arlok.com
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