At Pharmapack Europe, TekniPlex Healthcare plans to tout its expanded capacity for injection blow molded bottles and ...

健帆生物公告，全资子公司健帆血液净化公司于近日收到欧盟公告机构通知，其产品血浆分离器获得按照欧盟医疗器械法规Medical Devices Regulation（EU）2017/745（MDR）签发的欧盟MDR认证，可在欧盟国家及其他认可欧盟CE认证国家销售。

Several rules and regulations have important due dates in 2025 and beyond for which medical device manufacturers should be ...

The Healthcare Equipment and Allied Products Providers Association of Nigeria (HEPAN) has called on the federal government to tackle the challenges of debts, multiple regulatory requirements and high ...

The inspection robots market is projected to reach $5,593.6 million by 2031, at a CAGR of 21.6% from 2024 to 2031.

FG to look into cost of equipment, double registrations, others … expresses concern over delayed payment for equipment ...

“Vendors and contractors supplying critical equipment to public hospitals often experience payment delays of two to three years,” he lamented, noting that the delays are attributed to the indifference ...

Martin Makary, a Johns Hopkins surgeon and researcher, has been critical of the FDA. He could have the most influence over device policy among Trump’s nominees. CEO Dev Kurdikar said the decision may ...

Technologies developed by UC San Diego and Scripps Research teams will map the human eye-brain connectome, extend the ...

This webinar will examine Section 522 of the Federal Food, Drug, and Cosmetic Act (FD&C Act), as well as appropriate articles/Annexes of the EU's MDR, which require manufacturers to conduct ...

PMBI blacklists six medicine suppliers in five years for non-compliance with quality standards: Gireesh Babu, New Delhi Wednesday, December 4, 2024, 08:00 Hrs [IST] The Pharmaceut ...

In this edition of Three Questions, health care & life sciences partner Nate Brown spoke with Jeremy Schutz, director of business development, ...