Keep Informed on Legal and Compliance Developments Affecting Diagnostic Labs
Best practices and expert insight to help lab professionals comply with regulations and identify strategic trends in business and technology
Already a Subscriber? Log in Here
Lab Industry Advisor Subscription
Struggling with Staying Informed? In the fast-paced world of diagnostic medicine, staying updated with the latest legal, compliance, regulatory, and industry insights is crucial. Yet, finding reliable and comprehensive information can be overwhelming and time-consuming.
Lab Industry Advisor to the Rescue! Lab Industry Advisor provides comprehensive, up-to-date insights and analyses tailored to your needs. With expert commentary and actionable advice, you’ll stay ahead of the curve. No more sifting through endless sources—everything you need is right here!
Start your free trial today and see how Lab Industry Advisor can transform your approach. Get instant access to invaluable resources designed to keep you informed and competitive. Explore detailed reports, in-depth articles, and exclusive industry insights that help you make better decisions faster. Choose from three subscription levels tailored to fit your needs: Essential, Premium, and Elite.
Additional Business Intelligence Offerings
Clinical Diagnostics Insider
Keeps you up-to-date on new diagnostic tests, testing trends and opportunities, and emerging test technologies
Virtual Events & Webinars
Virtual events & webinars offer a variety of solutions and strategies for dealing with key issues labs face.
Lab Industry Advisor Subscriptions Include
Analysis and insight on key compliance, legal, and business developments affecting laboratories
- Updates on changes to regulations
- Healthcare-related laws
- FDA approvals
- Business deals in the diagnostics space, and more
Latest Articles
LDTs Rule Update: More Support for Legal Challenges Against FDA
Key clinical laboratory organizations file amicus brief, reiterating that the FDA is overstepping its authority, and its new rule would cause “irreparable patient harm”
New FDA LDTs Guidance Offers Useful Summary, But Questions Remain
Recently released document for small labs offers a more digestible version of the final rule requirements but still lacks key details
CMS Slated to Close Change Healthcare Payment Program
Program meant to ease cash flow disruptions experienced by some Medicare providers and suppliers due to the cyberattack will conclude in mid-July
Rosetta Genomics Closes Deal to Acquire PersonalizeDx
By Ron Shinkman, Editor, Laboratory Industry Report New Jersey-based Rosetta Genomics has closed a deal to acquire CynoGen, Inc., which does business as PersonalizeDx, for $3.9 million in cash and stock. Rosetta acquired PersonalizeDx from California-based Prelude...
Expedited FDA Approval Process Begins for Diagnostic Devices Addressing Unmet Needs
By Kelly A. Briganti, Editorial Director, G2 Intelligence Starting April 15, the FDA will begin implementing an expedited approval process for devices subject to premarket approval or de novo requests that can satisfy unmet needs for life-threatening or...
EHRs Deficient in Lab Test Result Graphing Capabilities
By Lori Solomon, Editor, Diagnostic Testing & Emerging Technologies Many current commercial electronic health records (EHRs) have "significant limitations" in graphing laboratory test results, according to a study published online March 19 in the Journal...
Cancer Risks Differ by Type of BRCA1 and BRCA2 Mutation, Study Finds
By Stephanie Murg, Managing Director, G2 Intelligence Although an extensive body of research links inherited mutations in the BRCA1 and BRCA2 genes to breast and ovarian cancer, little is known about the relationship between specific mutations and cancer risk—until...
Roche, Foundation Medicine Close Their Strategic Transaction
By Ron Shinkman, Editor, Laboratory Industry Report Foundation Medicine and pharmaceutical giant Roche have closed their $1.03 billion strategic transaction, the two companies have announced this week. Under the terms of the deal, Roche has purchased 15.6 million...
Drug Testing Doctor Gets Jail Sentence For Medicaid Fraud
By Christopher P. Young, Editor, G2 Compliance Advisor A Brookline Massachusetts physician, Dr. Punyamurtula Kishore, and his company Preventive Medicine Associates, Inc. (PMA), pleaded guilty to fraudulently billing Massachusetts's Medicaid program, MassHealth,...
23andMe’s Approval Marks ‘Baby Step’ in DTC
...
Register
Routine Mass Spec Urine Drug Testing Gaining Traction
...
Register
Universal, Extensive MRSA Screening Too Expensive for Hospitals
...
Register
More Comprehensive View of Laboratory Automation Unfolding
...
Register