This document certifies thatAron Whitehas successfully completed and is deemed competent for:Certified Quality Manager - Medical DevicesCERTIFICATE OF COMPETENCE
Velocity 360 USA Training is an Exemplar Global certified training provider for the training modules listed above.For and on behalf of Velocity 360 Training___________________________ M. Todd Crowder, Vice President Professional Education Services Velocity 360 USA Training LLCIssue Date: April 29, 2021 CEUs Awarded: 4.6 Certificate Number: 59808825 Expiration Date: April 30, 2024
This credential is digitally verifiable and secure. Scan the QR Code above with smartphone to verify credential.The ISO 13485 Certified Quality Manager - Medical Devices is a 46-hour training program that includes 4 courses; ISO 13485:2016 Lead Auditor, ISO 14971:2019 Medical Device Risk Management Requirements, FDA 21 CFR 820 cGMP Requirements, Good Documentation Practice, and the principles and practices of leading management system audits in accordance with ISO 19011:2018 Guidelines for Auditing Management Systems.
Information and Contact: Velocity 360 USA Training. Email: support@velocity360training.com Tel: 1-888-345-0322 | Online: www.velocity360training.com. This certificate was issued electronically and remains property of Velocity 360 USA Training and is bound by the Terms of Use.
The ISO 13485 Certified Quality Manager - Medical Devices is a 46-hour training program that includes 4 courses; ISO 13485:2016 Lead Auditor, ISO 14971:2019 Medical Device Risk Management Requirements, FDA 21 CFR 820 cGMP Requirements, Good Documentation Practice, and the principles and practices of leading management system audits in accordance with ISO 19011:2018 Guidelines for Auditing Management Systems.
Aron White
The ISO 13485 Certified Quality Manager - Medical Devices is a 46-hour training program that includes 4 courses; ISO 13485:2016 Lead Auditor, ISO 14971:2019 Medical Device Risk Management Requirements, FDA 21 CFR 820 cGMP Requirements, Good Documentation Practice, and the principles and practices of leading management system audits in accordance with ISO 19011:2018 Guidelines for Auditing Management Systems.
Skills / Knowledge
- VP Quality
- Quality Manager
- Quality Director
- Quality Engineer
- Lead Auditor
- VP Regulatory Affairs
- Regulatory Affairs Manager
- Regulatory Affairs Specialist
- ISO 13485 Compliance
- Medical Device Risk Management
- Good Documentation Practices
- Quality Management Systems
- Regulatory Compliance
Issued on
Expired on
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