News & Insights
Read the latest LSO medical device manufacturing, packaging, and sterilization insights featuring reliable resources and industry expertise you can count on. Industry updates, technical guides, company news, and practical insights on medical device manufacturing, packaging, sterilization, and supply chain strategy from LSO.
How Innovation, Access, and Regulation Are Reshaping the Future of IVD
Read ArticleShould You Rent or Build Your Cleanroom? A Diagnostic for Medical Device Startups
Renting a cleanroom offers medical device companies speed, scalability, and compliance—without the capital burden of building your own.
Read ArticleFew and Far Between: Why CDER-Certified Steam Sterilization—and the Experts Behind It—Matter for Combination Product OEMs
Few providers meet FDA CDER standards for steam sterilization. This blog explains what certification involves and why capacity and in-house expertise matter for OEMs.
Read ArticleKrista Precourt Named COO of LSO: Strengthening Our Commitment to Clients
Krista Precourt is named COO of LSO, reinforcing medical device manufacturing leadership through expert operations and scalable client support.
Read ArticleStandard Tests for Evaluating Packaging During Transportation
Explore package transportation testing to ensure your medical devices arrive safely and sterile despite rough handling.
Read Article25 Years of Leadership in Quality: Celebrating Mireya Lozano’s Impact at LSO
Celebrating Mireya Lozano’s 25 years at LSO—her leadership in quality and regulatory has shaped our success in medical device manufacturing and compliance.
Read ArticleIs Vaporized Hydrogen Peroxide (VH2O2) the Right Sterilization Method for Your Medical Device?
Find out if VHP sterilization is suitable for your medical devices and explore alternatives for optimal sterilization results.
Read ArticlePre-Validated Packaging: Choosing the Right Fit
Learn if your medical device issuitable for pre-validated packaging solutions with our free 'Will It Fit?' calculator.
Read ArticleHow Often Should Packaging Validation Be Revisited?
Find out how frequently your packaging validation needs to be revisited with our free Packaging Validation diagnostic tool
Read ArticleWhat Are the Latest Updates to ASTM F1980 for Accelerated Aging?
Stay current on ASTM F1980 updates and changes, and how they impact sterile packaging validation and shelf-life claims.
Read ArticleWhat do Medical Device OEMs Need to Know for MDR CE Mark Recertification in Europe?
Meeting the stringent new CE mark recertification MDR requirements will take time, planning, and expertise. This is what you need to know to get started.
Read ArticleNIST 800-171 Compliance
LSO achieves NIST 800-171 compliance, showcasing their commitment to cybersecurity in the medical device industry.
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