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Global Medical Device Regulatory Strategy by Various Contributors, Prithal Bom, Gert Bos, David Brindley, Joanna Brougher, Andrew Carr, Stanely Chalvire, Tony Chan, Xianjun Chen, Mark Chipperfeld, Raymond Chua, Stewart Crumpler, Benjamin Davies, Sean Detweiler, Scott Dickerhoff, Sue Dopson, David Fazzolare, Melissa Gaynor, Elisabeth George, Jeffrey Gibbs, Ann Goodall, Dorota Grabowska, Susan Hibbeln, Tom Hutchinson, Chie Iwaishi, Jocelyn Jennings, Amit Kukreja, Michael C. Morton, Allyson Mullen, Nobuko Nakajima, Dawn Norman, Penny Northcutt, Matthew O'donnell, Gretchen Parker, Sethuraman Rama, Taranjit Samra, Philip Sax, Maria Shepherd, Michael Siano, James Smith, Manuel Urena, Brian Young, Melissa Walker, Lisa Warren, Karolina Wartolowska, Pamela Weagraff, Michelle Wu Hardcover, 320 Pages, Published 2016 by Regulatory Affairs Professionals Society (Raps) ISBN-13: 978-0-9969491-3-2, ISBN: 0-9969491-3-5 |
Medical Device Software Software Development LifeCycle Methodologies, Tools and Risk Management by Taranjit Samra Paperback, 212 Pages, Published 2013 by Scholar's Press ISBN-13: 978-3-639-51472-8, ISBN: 3-639-51472-6 |
Taranjit Samra