New Course

The purpose of this procedure is to ensure that records and data within your quality management system are controlled in such a way that they remain legible, readily identifiable, and retrievable for at least as long as is required by regulatory requirements and your business needs. We now include color-coded cross-references to the specific clauses in the ISO 13485:2016 standard and Regulation (EU) 2017/745. This is to help auditors quickly find where the applicable requirements are in the procedure.

About the course

Includes: - SYS-002, Control of Records Procedure - Webinar and Slides - FRM-003, Record Destruction Form - Good Documentation Practices Webinar - Good Documentation Practices Quiz - Training Certificate

Curriculum

2 Chapters · 7 Lessons

1
1. (Included in full purchase)
  SYS-002: Control of Records Procedure Webinar
2. (Included in full purchase)
  SYS-002: Control of Records Procedure (Slides)
3. (Included in full purchase)
  SYS-002: Control of Records Procedure
4. (Included in full purchase)
  FRM-003: Document Destruction
2
1. (Included in full purchase)
  Good Documentation Practices Webinar
2. (Included in full purchase)
  Good Documentation Practices (Slides)
3. (Included in full purchase)
  Quiz: Good Documentation Practices

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