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Medical Device Research and Development Compliance Training and Best Practices
Medical device Research and Development (R&D) based webinars, in-person seminars, standards and best practices for medical device R&D professionals – process validation, FMEA, QbD, ISO13485, ISO 14971, Design Control and Product Validation, Design History Files, Technical Files, Design Dossiers, etc.Sub Categories:
Drug R & D
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Device R & D
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By: Miles HutchinsonAdd to CartPrice: $249
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Add to CartSan Francisco, CA | Aug 6-7, 2020
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Add to CartVirtual Seminar | Jul 16-17, 2020
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Add to CartVirtual Seminar | Jun 18-19, 2020
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Add to CartLos Angeles, CA | Aug 20-21, 2020
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Add to CartVirtual Seminar | Jul 16-17, 2020
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Add to CartVirtual Seminar | Jun 25-26, 2020
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Add to CartVirtual Seminar | Jun 10, 2020
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Add to CartVirtual Seminar | Jun 3-4, 2020
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Add to CartVirtual Seminar | Jul 6-7, 2020
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Add to CartSan Francisco, CA | Oct 22-23, 2020
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Add to CartVirtual Seminar | Jul 9-10, 2020
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Add to CartVirtual Seminar | Jun 3-4, 2020
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Add to CartVirtual Seminar | June 3-4, 2020
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Add to CartMiami, FL | Jul 29-31, 2020
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Add to CartVirtual Seminar | Jun 17, 2020
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Provider: ANSIAdd to CartPrice: $142
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Provider: ANSIAdd to CartPrice: $120
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Provider: ANSIAdd to CartPrice: $250
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Provider: SEPTAdd to CartPrice: $299
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Provider: Quality-Control-PlanAdd to CartPrice: $37
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Provider: At-PQCAdd to CartPrice: $397
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