International regulatory and compliance services firm selects clinivation WorldView as its most comprehensive, authoritative resource for building medical product submissions and registrations worldwide.
Framingham, MA, May 1, 2007 – clinivation, Inc. announced today that Resolute Regulatory Consulting Services has selected clinivation WorldView™.
“We are pleased to have Resolute as a subscriber to clinivation WorldView,” said Richard Morroney, R.A.C., C.Q.A., clinivation’s Vice President of Regulatory and Quality Solutions. “Resolute and clinivation share the same vision- to make better medical products and bring them to market faster than ever before. Clinivation WorldView will enable the development of regulatory strategies for >99% of the world markets,” he continued.
Clinivation WorldView is your most comprehensive, authoritative, and up-to-date resource for building all of your medical device submissions and registrations worldwide. Clinivation WorldView also interoperates with clinivation Global® enterprise software to make building and tracking medical device submissions and registrations easier than ever before.
About Resolute Regulatory Consulting Services, Inc.
Resolute Regulatory Consulting Services brings over 30 years of regulatory, quality, manufacturing, and research and development expertise to the medical device, pharmaceutical, combination drug/device, and biologic industries. Resolute has successfully formulated global regulatory strategies, international product registrations, and expansion of clinical trials from feasibility to the pivotal stage. Resolute has successfully directed negotiation both domestically, with USFDA, and internationally, with various European Notified Bodies and Japan MHLW.
