FDA 21 CFR Part 820 vs.

ISO 13485:2016
Comparison Table created by greenlight.guru
FDA QSR (21 CFR Part 820) ISO 13485:2016
820.1 Scope 1 Scope
2 Normative References
820.3 Definitions 3 Terms and Definitions
820.5 Quality System 4 Quality Management System
4.1 General Requirements
4.2 Documentation Requirements
820.20 Management Responsibility 5.0 Management Responsibility
820.20(a) Quality Policy 5.3 Quality Policy
820.20(b) Organization 4.1 Management Responsibility –
General
820.20(b)(1) Responsibility & Authority 5.5 Responsibility & Authority
820.20(b)(2) Resources 5.1e Management Commitment
820.20(b)(3) Management 5.5.2 Management Representative
Representative
820.20(c) Management Review 5.6 Management Review
820.20(d) Quality Planning 5.4 Quality Planning
820.20(e) Quality System Procedures 4.2.1 General
4.2.2 Quality Manual
820.22 Quality Audit 8.2.4 Internal Quality Audits
820.25 Personnel 6 Resource Management
820.25(a) General 6.1 Provision of Resources
6.2 Human Resources
820.25(b) Training 6.2 Human Resources
820.30 Design Controls 7.3 Design and Development
820.30(a) General 7.3 Design and Development
820.30(b) Design and Development 7.1 Planning of Product Realization
Planning 7.3.2 Design and Development
Planning

© 2016

Quality Management Software Exclusively for Medical

820.30(c) Design Input 7.2.1 Customer Related Processes
7.2.2 Review of Requirements
Related to Product
7.3.3 Design and Development
Inputs
820.30(d) Design Output 7.3.4 Design and Development
Outputs
820.30(e) Design Review 7.3.5 Design and Development
Review
820.30(f) Design Verification 7.3.6 Design and Development
Verification
820.30(g) Design Validation 7.3.7 Design and Development
Validation
820.30(h) Design Transfer 7.3.8 Design and Development
Transfer
820.30(i) Design Changes 7.3.9 Control of Design and
Development Changes
820.30(j) Design History File 7.3.10 Design and Development
Files
820.40 Document Controls 4.2.4 Control of Documents
820.40(a) Document Approval and 4.2.4 Control of Documents
Distribution
820.40(b) Document Changes 4.2.4 Control of Documents
820.50 Purchasing Controls 7.4.1 Purchasing Process
820.50(a) Evaluation of Suppliers, 7.4.1 Purchasing Process
Contractors, and Consultants
820.50(b) Purchasing Data 7.4.2 Purchasing Information
7.4.3 Verification of Purchased
Product
820.60 Identification 7.5.8 Identification
820.65 Traceability 7.5.9 Traceability
820.70(a) Production and Process Controls 7.5.1 Control of Production and
Service Provision
7.5.6 Validation of Processes for
Production and Service Provision
820.70(b) Production and Process 6.3 Infrastructure
Changes 6.4 Work Environment and
Contamination Control
7.5.1 Control of Production and
Service Provision
7.5.6 Validation of Processes for
Production and Service Provision
820.70(c) Environmental Control 6.4 Work Environment and
Contamination Control
820.70(d) Personnel 6.2 Human Resources
820.70(e) Contamination Control 6.4.2 Contamination Control
820.70(f) Buildings 6.3 Infrastructure
820.70(g) Equipment 6.3 Infrastructure
7.5.1 Control of Production and
Service Provision
7.5.6 Validation of Production and
Service Provision
820.70(h) Manufacturing Material 7.5.11 Preservation of Product
820.70(i) Automated Processes 6.3.b Infrastructure
7.5.6 Validation of Production and
Service Provision
820.72 Inspection, Measuring, and Test 7.6 Control of Monitoring and
Equipment Measurement Equipment
820.75 Process Validation 7.5.6 Validation of Production and
Service Provision
820.80(a) Receiving, In-‐process, and 7.1 Planning of Product Realization
Finished Device Acceptance – General 7.4.3 Verification of Purchased
Product
7.5.1 Control of Production and
Service Provision
820.80(b) Receiving Acceptance 7.4.3 Verification of Purchased
Product
820.80(c) In-‐Process Acceptance 7.1 Planning of Product Realization
820.80(d) Final Acceptance Activities 7.1 Planning of Product Realization
820.80(e) Final Acceptance Records 7.1 Planning of Product Realization
820.86 Acceptance Status 7.5.8 Identification
820.90(a) Non-‐Conforming Product 8.3 Control of Nonconforming
Product
820.90(b) Nonconformity Review and 8.3 Control of Nonconforming
Disposition Product
820.100 Corrective and Preventative 8.5.2 Corrective Action
Action 8.5.3 Preventative Action

820.120 Device Labeling 4.2.3 Medical Device File

7.5.8 Identification
7.5.11 Preservation of Product
820.130 Device Packaging 4.2.3 Medical Device File
7.5.8 Identification
7.5.11 Preservation of Product
820.140 Handling 4.2.3 Medical Device File
7.1 Planning of Product Realization
7.5.8 Identification
7.5.11 Preservation of Product
820.150 Storage 4.2.3 Medical Device File
7.1 Planning of Product Realization
7.5.8 Identification
7.5.11 Preservation of Product
820.160 Distribution 4.2.3 Medical Device File
7.1 Planning of Product Realization
7.5.8 Identification
7.5.11 Preservation of Product
820.170 Installation 4.2.3 Medical Device File
7.5.3 Installation Activities
7.5.8 Identification
7.5.11 Preservation of Product
820.180 Records 4.2 Documentation Requirements
4.2.3 Medical Device File
7.1 Planning of Product Realization
820.181 Device Master Record 4.2.3 Medical Device File
820.184 Device History Record 4.2.5 Control Records
7.1 Planning of Product Realization
7.5.8 Identification
820.186 Quality System Record 4.2 Documentation Requirements
7.1 Planning of Product Realization
820.198 Complaint Files 7.2.3 Communication
8.2.1 Feedback
8.2.2 Complaint Handling
8.2.3 Reporting to Regulatory
Authorities
820.200 Servicing 4.2.3 Medical Device File
7.1 Planning of Product Realization
7.5.4 Servicing
7.5.8 Identification
820.250 Statistical Techniques 8.1 General
8.4 Analysis of Data

g
r
e
e
n
l
 ight.guru’s eQMS solution is being used by some of the world’s most
innovative medical device companies all over the globe to help ensure their
compliance to ISO 13485:2016 and FDA 21 CFR Part 820.

Visit www.greenlight.guru to learn more about our software + services and see
how we might be able to help your company.