This document certifies thatDiana Wieckowskihas successfully completed and is deemed competent for:Medical Devices - FDA 21 CFR 820 cGMP | RequirementsInformation 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.CERTIFICATE OF COMPETENCE
Velocity 360 USA Training is a certified training provider for the training modules listed above.For and on behalf of Velocity 360 USA Training___________________________________________ M. Todd Crowder, Vice President, Office of Registrar Professional Education Services Velocity 360 USA Training, LLCIssue Date: October 5, 2021 CEUs Awarded: 0.6 Certificate Number: 39667132 Expiration Date: October 31, 2024
This credential is digitally verifiable and secure. Scan the QR Code above with smartphone to verify credential.This 6-hour training course teaches a detailed understanding and concepts of the Quality System Regulations (QSR) and Current Good Manufacturing Practices (CGMP), required by the United States FDA 21 CFR 820 regulations for Medical Devices.
This document certifies that
Diana Wieckowski
has successfully completed and is deemed competent for:
Medical Devices - FDA 21 CFR 820 cGMP | Requirements
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.
CERTIFICATE OF COMPETENCE
Velocity 360 USA Training is a certified training provider for the training modules listed above.
For and on behalf of Velocity 360 USA Training
___________________________________________
M. Todd Crowder, Vice President, Office of Registrar
Professional Education Services
Velocity 360 USA Training, LLC
Issue Date: October 5, 2021
CEUs Awarded: 0.6
Certificate Number: 39667132
Expiration Date: October 31, 2024
This credential is digitally verifiable and secure. Scan the QR Code above with smartphone to verify credential.
This 6-hour training course teaches a detailed understanding and concepts of the Quality System Regulations (QSR) and Current Good Manufacturing Practices (CGMP), required by the United States FDA 21 CFR 820 regulations for Medical Devices.
Diana Wieckowski
This 6-hour training course teaches a detailed understanding and concepts of the Quality System Regulations (QSR) and Current Good Manufacturing Practices (CGMP), required by the United States FDA 21 CFR 820 regulations for Medical Devices.
Skills / Knowledge
- Regulatory Affairs Manager
- Regulatory Director
- Regulatory Specialist
- VP Regulatory Affairs
- Quality Director
- VP Quality
- Quality Manager
- Quality Engineer
Issued on
October 5, 2021
Expired on
October 31, 2024