There are several key security concerns neurotech developers must address from the outset to ensure both medical and ethical ...

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 ...

We are sure you are aware that the EU medical devices framework has been subject to significant changes over recent years. However, implementation of the new rules has been problematic since the ...

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 ...

Surface Modifying End Groups (SMEs) are surface-active oligomers covalently bonded to the base polymer during synthesis. Surface Modifying End Groups (SMEs) are surface-active oligomers covalently ...

This seal strength tester measures the seal strength of porous and non-porous flexible packages using inflation This seal strength tester measures the seal strength of porous and non-porous flexible ...