Clinivation WorldView is your most comprehensive, authoritative resource for building all of your medical device submissions and registrations worldwide.
Framingham, MA, October 16, 2006 – clinivation, Inc. announced today the release of clinivation WorldView Online Global Regulatory Intelligence Solution.
“Because clinivation WorldView provides users with access to over 99% of the world markets, regulatory affairs departments will stay current with ever-changing regulations faster and easier than ever before,” said Joseph Kozikowski, M.D., clinivation’s Founder, Chairman, and Chief Executive Officer. “Clinivation WorldView delivers everything you need in one place- from clear explanations of the country-specific registration processes, to the essential regulatory contacts, forms, and templates,” he continued.
“The days of piecing together out-of-date and conflicting information from distributors and untranslated documents are over. Clinivation WorldView is the most comprehensive, authoritative resource for building all your medical device approvals and registrations worldwide,” remarked Richard Morroney, R.A.C., C.Q.A., clinivation’s Vice President of Quality and Regulatory Solutions.
Clinivation WorldView also interoperates with clinivation Global™ enterprise software to make building and tracking medical device submissions and registrations easier than ever before.
