Nothing contained in Art. 501 is unimportant, but some of its requirements may merit extra attention. To make sense of the potential pitfalls and conflicts, begin outside of Art. 501. Specifically, ...

The regulations governing the viable and nonviable management of Class D clean zones indicate that necessary actions should be determined on a site-by-site, risk-based assessment. According to the FDA ...

The scope of FDA requirements, such as pre-market regulatory approvals, that apply to companies offering genetic tests depend almost entirely on the nature of the genetic test offered. In some cases, ...

Major amendments to Canadian trademark law took effect on 17 June 2019. Although five years had elapsed between when the amendments were first passed and the date that they came into force, many ...

Of the three types of Hazardous Locations, Class III has the least stringent requirements. Fibers (and flyings) have a much larger particle size than dust (Class II) or gases (Class I). That makes ...