FDA / CDRH Submissions Services

We have made a good name in the market for FDA / CDRH Submissions Services. All laser products entering the USA must be registered with the FDA to legally enter the country In the USA laser safety is dealt with by regulations which are part of federal law (as opposed to Europe where manufacturers self certify to various product standards). CDRH, which is part of FDA, has the task of enforcing the regulations. The laser product regulation is known as 21 CFR 1040.10. Want more details on FDA / CDRH Submissions Services? Please contact us on +44 0 1202 770740!

For more information on FDA / CDRH Submissions Services talk to Lasermet