Article 16 of the European Union’s Medical Device Regulation and In Vitro Diagnostic Regulation specifically address the ...

In the medical device industry, FDA inspections are not a regulatory hurdle — they are a powerful tool for improving product quality, operational efficiency, and patient safety. Shift from a reactive ...

Experience the next generation of biopharma innovation with PharmaLok™ ZerO sanitary clamps. Designed to simplify and streamline biopharma processes, these advanced clamps feature a universal fit and ...

The DEA has announced new rules for remote prescription of controlled substances. As telehealth adoption grows, regulatory ...

Loveland, CO - Nordson MEDICAL, a Nordson Company (Nasdaq: NDSN), is thrilled to unveil PharmaLok™ ZerO sanitary clamps, an innovative solution designed to replace traditional TC clamps in the ...

The updated requirements for post-market surveillance (PMS) under the EU Medical Device Regulation (MDR), EU In Vitro Diagnostics Regulation (IVDR), and the U.K.'s forthcoming Statutory Instrument (SI ...

READYcut is an innovative bench-top programmable cutting machine for medical grade tubing, with a system for solvent dispensing on the tube end READYcut is an innovative bench-top programmable cutting ...

Quality is an ever-growing problem in the fields of pharmaceutical, medical devices, medical diagnostics and biologics, and its negative impact is signifi cantly palpable to manufacturers as well as ...

Not long ago, many experts in the pharmaceutical industry were looking at the so-called patent cliff of small molecules and wondering where the next blockbuster drug or therapy innovation would come ...