The global preclinical medical device testing services market is poised for steady expansion, with revenue expected to grow from USD 1,696.0 million in 2025 to USD 2,842.1 million by 2035, at a CAGR ...
The National Association of Boards of Pharmacy (NABP) plays an important role in the state licensing of prescription medical device manufacturers ...
As of late February, there were 147 medical device recall events and 20 of them, or 13.6%, were Class I, according to a Modern Healthcare report.
The IEC Conformity Assessment System for Electrotechnical Equipment and Components (IECEE) has been building trust for ...
A combination of long-standing federal, provincial or territorial regulations or standards ... by means of UV radiation. Devices that operate by means of UV radiation that are classified as a Class II ...
In the medical device industry, usability plays a critical role in ensuring the safety and effectiveness of highly complex ...
SINGAPORE – Regulations against online marketplace platforms and retailers selling non-compliant active mobility devices will be introduced here, said Senior Parliamentary Secretary for ...
The American Renewable Energy Standards and Certification Association (ARESCA) is notifying all directly and materially ...
Potential Medicare coverage reforms, such as eliminating Coverage with Evidence Development, would remove key policy tools ...
It was imperative for a large European CMO that produces multiple biologic drugs to select the right product quality and ...
Regulatory developments include FERC’s actions on electric storage resources participating in the wholesale markets, co-location of large ...
Experts discuss how cancer treatment and survivorship can be made more equitable and affordable through advocacy, outreach, and effective communication tools. Beyond Cancer: Caring for Young ...
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