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Disclaimer

This website, all toolkits, templates, and content are provided for informational and educational purposes only. They are not legal, regulatory, or professional advice. Use at your own risk. Always consult qualified professionals before making decisions.

Terms of Use

By purchasing and using the Medical Device Training Records Toolkit, you agree that all materials are provided "as is" without warranty of any kind. The templates are starting points that must be customized to your specific organizational needs and validated by qualified professionals within your organization.

You receive a single-entity license to use, modify, and distribute the templates within your organization. Redistribution or resale of the original templates is prohibited.

Regulatory Notice

While our templates reference FDA 21 CFR 820.25 and ISO 13485 Section 6.2 requirements, regulatory standards are subject to change. Users are responsible for ensuring their quality management system documentation meets current applicable regulatory requirements. These templates do not guarantee regulatory compliance.

Refund Policy

Due to the digital nature of this product, all sales are final. If you experience any issues with your purchase, please contact us at leroy@regwatchdaily.com and we will work to resolve the matter.

Privacy Policy

We collect only the information necessary to process your purchase and deliver your product, including your name, email address, and payment information. Payment processing is handled securely by Stripe. We do not store your payment card details. We may send you product updates and related information to the email address provided at purchase.

Contact

For questions about these terms or our products, contact us at leroy@regwatchdaily.com.