Description

Maven was established in 2016 with a forward-thinking vision of being the ultimate service provider for medical device regulatory affairs, covering a wide range of global regulations. We aim to become one-stop destination for all medical device manufacturers who place their trust in us to get things done. Our core service is technical documentation, writing which is complimented by other ancillary services we offer, allowing clients to avoid the need to engage multiple partners for different aspects related to product certification and registration.