Medical Device Industrial Services In Usa Texas
8 services found
by:Emergo by UL based inAustin, TEXAS (USA)
Commercializing your medical device first requires you to obtain registration and approval from regulatory agencies in each country where you plan to sell your device. Device registration requirements can vary significantly from country to country, which can create compliance challenges for companies pursuing multiple-market strategies. Depending on where you plan to sell your device(s), ...
by:Emergo by UL based inAustin, TEXAS (USA)
Medical device regulations in most countries require foreign manufacturers to appoint an in-country representative. Your representative acts as your liaison to regulatory authorities and assists with device registrations and vigilance/adverse event reporting. It’s important to choose a representative who is familiar with the regulatory requirements for your product to act in the best ...
by:Emergo by UL based inAustin, TEXAS (USA)
Regulators in most medical device markets require registrants to meet post-market surveillance (PMS) obligations to maintain compliance. However, PMS rules can vary between different medical device markets, requiring manufacturers to develop tailored rather than one-size-fits-all approaches. With deep expertise in post-market surveillance requirements, Emergo is equipped to act as your compliance ...
Manufactured by:Genesis Medical Plastics based inCypress, TEXAS (USA)
Genesis offers our specialized extrusion, calendering, injection molding and machining capabilities on a tolling basis to convert customers’ medical polymers into the stock shapes, films and components required for their medical ...
Manufactured by:Genesis Medical Plastics based inCypress, TEXAS (USA)
In addition to machining and injection molding specific components, Genesis can assist medical device manufacturers with assembly, laser marking, industry-compliant packaging and other services for a more efficient supply ...
by:CSA Group based inToronto, ONTARIO (CANADA)
Mitigate the risk of a cyber attack with thorough review and testing of your connected products and systems. Cybercrime damage costs are expected to hit $6 trillion annually by 2021, up from $3 trillion in 2015. IoT devices connect twice as many people that are alive in the world. In 2015, the FBI warned about the dangers of IoT, yet most devices are still ...
by:Emergo by UL based inAustin, TEXAS (USA)
It is easy to make mistakes in the regulatory process that can delay market entry or incur unnecessary costs. With help from Emergo’s medical device RA/QA consultants, you can pursue the most efficient regulatory route to approval and registration for your device, and maintain compliance with post-market requirements ...
by:Tietronix Software, Inc. based inHouston, TEXAS (USA)
Tietronix has the knowledge and tools to accelerate your project technologies. While our expertise is in the medical field, including pharmaceutical, biotechnology, medical devices, and health care administration sectors, we can work in any ...