There are several key security concerns neurotech developers must address from the outset to ensure both medical and ethical compliance, as well as commercial success.

Given the calls for change, criticism, and ongoing consultations, this article sets out the current status of developments and what is important to know when seeking to do business in the EU.

Sensor-based digital health technologies (sDHTs), including wearables, have great potential in the management of mental ...

Watch a comprehensive overview of regulatory requirements and testing standards relevant to disinfectant and cleaning validation in pharmaceutical and medical manufacturing. It begins with a ...

The medical technology sector in Europe is undergoing significant regulatory transformations, particularly in Switzerland and the U.K. These changes are shaping how medical devices are approved, ...

Explore the critical aspects of ophthalmic drug and device testing, emphasizing regulatory and patient compliance. It highlights the importance of ensuring safety, efficacy, and adherence to stringent ...

Eurofins Medical Device Services’ San Jose, CA, Ethylene Oxide (EO) sterilization site provides high-quality, fast-turnaround contract sterilization and validation services for the medical device ...

Medical device labeling must show many elements, such as manufacturer information, product information, intended use, indications for use, instructions for use, information regarding sterile ...

The Clear Solution. Daikyo Crystal Zenith ® vials provide a high-quality alternative to traditional glass vials. Daikyo Crystal Zenith vials reduce the risk of breakage within cold storage ...

The company designs and builds automated dip molding and dip coating machinery for the manufacturing of medical disposables such as catheters. ACC Automation Co. designs and builds automated dip ...