Today's medical device OEMs face many challenges such as;
- Evolving innovation cycles
- Product re-engineering
- Stringent regulatory norms and
- New market demands
With so many advancements in technology, it is imperative for the businesses to evolve at a faster pace, design smarter products while lowering the time to market and improving their operations.
LTTS’s concept-to-commercialize capabilities and in-depth technical expertise helps the customers throughout their medical device product development life cycle and help them lower the time to market & reduce the cost of operations. LTTS delivers end-to-end product development solutions through concept design, new product development, value engineering, sustaining engineering and V&V.
Over the years, LTTS has developed smarter products for global clients, from the design board to the shop floor and out to the market.
WHAT WE DO
DOING THINGS DIFFERENTLY
Our mature PDLC process framework follows ISO 13485 guidelines and our risk management approach is aligned to ISO14971
Our in-house compliance testing facilities strictly adheres to IEC 61010, IEC 60601-1-1 3rd edition, and 60601-1-2 4th edition
Our team of experts brings device engineering expertise in multiple domains across Class I, Class II and Class III medical