Clinivation WorldView has now achieved the position of the medical device industry’s most comprehensive resource for IVD regulatory intelligence worldwide.
Framingham, MA, May 17, 2007 – clinivation, Inc. announced today that clinivation WorldView™ Online Regulatory Intelligence has now achieved the position of the medical device industry’s most comprehensive resource for IVD regulatory intelligence worldwide.
“With the expansion of IVD intelligence, clinivation WorldView has achieved the most comprehensive, authoritative, and up-to-date resource for IVD and medical device regulatory intelligence,” remarked Richard Morroney, R.A.C., C.Q.A., clinivation’s Vice President of Quality and Regulatory Solutions. “Our subscribers have complete, unlimited, annual access to the medical device and IVD registration processes for >99% of the world markets allowing them to stay current on ever changing worldwide regulations,” he continued.
Clinivation WorldView also interoperates with clinivation Global® enterprise software to make building and tracking medical device submissions and registrations easier than ever before.
