Avomeen’s extractables and leachables (E&L) team are attending AAPS PharmSci360 November 3-6, 2019 in San Antonio, Texas. If you’re able to attend, be sure to check out our poster, Development of a Library of Plastics Additives for Identification of Extractables. If you can’t make it to the show, we’ve got you covered.
Download our PosterDownload it Here
The FDA Gets Stricter with E&L Oversight, Can the Industry Keep Up? article in Contract Pharma, featuring Dr. Andrew Kolbert, Avomeen’s CTO, offers valuable insight.
In our years supporting the biopharma industry, we’ve seen some common mistakes made in E&L study design. We’ve outlined what not to do in our blog, Common Pitfalls in Ectractables & Leachables Testing.
Looking for a summary of USP guidelines for E&L testing? Our blog, The Long and Short of USP Guidelines for E&L Testing, offers some guidance.
Our blog, The Growing Need for Extractables & Leachables Testing of Pharmaceutical Manufacturing Equipment, offers information about FDA oversight and how CROs can help companies navigate the E&L process.
Learn more about FDA’s increasing oversight of E&L testing in pharma in Dr. Kolbert’s article in Tablets & Capsules Magazine.
Learn more about our proprietary plastic additive database in our blog, Best-In-Class Polymer Additive Library for Identification of Extractables.