Regulatory & Safety

Designing and building cleanrooms that meet today’s rigorous requirements takes careful planning and innovation

The need for clinical lab managers to communicate effectively ran the gamut from testing information to hiring and compliance

The FDA LDT rule would have imposed unnecessary burdens on laboratories, adding requirements beyond existing CLIA regulations

Here are several effective ways to reduce the risk of workplace injuries in your clinical laboratory

Bill Peters discusses why standard biosafety cabinets may not be enough for high-volume testing

Sustainability in lab chemicals is quickly becoming nonnegotiable—innovation shouldn’t come at the cost of our environment

ADLM congressional briefing explains the importance of laboratory developed tests for pediatric care and the FDA rule that will limit access to these critical tests

Innovative wastewater treatment methods helping labs reduce environmental impact

How centralized informatics solutions can eliminate data silos, improve traceability, facilitate compliance, and reduce turnaround time

The Leadership Summit, which takes place April 7-9 in Pittsburgh, will also tackle succession planning and clinical lab operations

Clinical lab veterans and newcomers have reason to monitor the shutdown of information from the Trump administration

How central labs can mitigate IVDR impact 

Acquisition will focus on expertise and innovation for diagnostics and healthcare customers

Ensure precision and compliance in fluid delivery with insights into advanced testing techniques and technologies

Solutions for mitigating error and improving precision in dose accuracy testing

Few legal or policy constraints apply to the global chemical inventories of an estimated 350,000 products, according to the Consortium for Children’s Environmental Health

The problem is that many medical reports aren’t written with patients in mind

The new guidance on artificial intelligence was published in JAMA by UTHealth Houston and Baylor College of Medicine researchers

Creating laboratory environments that prioritize scientific innovation and human well-being

Key deadlines and questions in vitro diagnostic manufacturers need to consider to comply with IVDR Amendment EU 2024/1860