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Josh
@orleron
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Joined: Mar 14, 2015
Last seen: Apr 11, 2025
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Topics: 59 / Replies: 36
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Topic
Discussion Topic: Clinical trials around the world
8 years ago
Forum
Clinical Trials for Medical Devices
Replies: 1
Views: 1121
Topic
Discussion Topic: Vagueness of GMP's
8 years ago
Forum
Quality Systems Management
Replies: 17
Views: 2918
Topic
Discussion Topic: When Quality Systems change in the middle of a project
8 years ago
Forum
Quality Systems Management
Replies: 10
Views: 1212
Topic
Discussion Topic: Managing the Product Life Cycle
8 years ago
Forum
Product Life Cycle and Product Management
Replies: 13
Views: 1390
Topic
Discussion Topic: Playing with IQ, OQ, PQ
8 years ago
Forum
Process Validation and Process Risk
Replies: 12
Views: 2765
Topic
Discussion Topic: Differences between ISO and FDA
8 years ago
Forum
Process Validation and Process Risk
Replies: 7
Views: 2302
Topic
Discussion Topic: Post-market surveillance
8 years ago
Forum
Device Documentation
Replies: 20
Views: 3888
Topic
Discussion Topic: Is the DHF a living document?
8 years ago
Forum
The Design History File
Replies: 26
Views: 6489
Topic
Discussion Topic: Verification vs. Validation
8 years ago
Forum
The Design History File
Replies: 14
Views: 1925
Topic
Discussion Topic: Easier regulatory in EU?
8 years ago
Forum
EU Regulatory Basics
Replies: 25
Views: 2863
Topic
Discussion Topic: Your Field or Profession
8 years ago
Forum
Introduction to Advanced Medical Device Development
Replies: 22
Views: 3167
Topic
Discussion Topic: Course conclusion and impressions
8 years ago
Forum
Consultants and Legal Basics
Replies: 137
Views: 16692
Topic
Discussion Topic: Your organizational type
8 years ago
Forum
Organizational Development in Device Companies
Replies: 122
Views: 10990
Topic
Discussion Topic: Risk Management, Risk Analysis
8 years ago
Forum
Risk Analysis for Medical Devices
Replies: 30
Views: 4545
Topic
Discussion Topic: Supplemental on DHF and DMR
8 years ago
Forum
Introduction to Design Controls
Replies: 34
Views: 6265
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