Clinivation Global™software helps everyone in your company access everything they need to build and track all your medical device submissions and registrations worldwide.
Framingham, MA, October 17, 2003 – clinivation, Inc. today announced the release of clinivation Global™ 2.0 Medical Device Approvals Solution, Enterprise Edition.
“Because clinivation Global™ enables medical device companies to sell more products to more countries faster and easier than ever before, clinivation Global™ delivers an outstanding ROI,” said Joseph Kozikowski, M.D., clinivation’s Founder, Chairman, and Chief Executive Officer. “We designed every aspect of clinivation Global™ to provide users with the easiest and most productive solution for approvals worldwide, and users everywhere are thanking us for freeing them from the drudgery and uncertainty intrinsic to their traditional approaches,” he continued.
The Going Global: Best Practices Online Seminar Series- where executives can acquire the knowledge, process, and best practices to build robust submissions and manage families of international medical device registrations- has been launched in conjunction with the release of clinivation Global™ 2.0.
Industry executives can register for these free, information-packed seminars with how-to advice, live demos, and Q & A online at www.clinivation.com/global
“The days of weeding through countless spreadsheets, digging through file cabinets, and hoping to get through to the one and only person who knows what’s going on are behind us. Clinivation Global™ is the first complete solution targeted at automating the business processes for medical device approvals worldwide,” remarked Richard Morroney, R.A.C, C.Q.A., clinivation’s Vice President of Quality and Regulatory Solutions.
