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Privacy Policy

Last updated: March 2026 · MedDev Advisory · Kanpur, India

1. Who We Are

MedDev Advisory is a medical device regulatory consulting practice operated by Arvind Rathore, based in Kanpur, India. We provide ISO 10993 biological evaluation, EU MDR, and FDA regulatory documentation services to medical device companies globally.

For privacy-related queries, contact us at: arvindrthr0607@gmail.com

2. What Data We Collect

When you use our contact form or communicate with us, we may collect:

  • Name and job title
  • Company name
  • Email address
  • Phone or WhatsApp number (if provided)
  • Project description and device information (as provided by you)
  • Regulatory target and submission timeline

We do not use tracking cookies, analytics scripts, or advertising networks on this website.

3. Why We Collect Your Data

Your data is collected solely to:

  • Respond to your inquiry about our services
  • Provide a project scope and proposal if requested
  • Communicate about ongoing or prospective projects

We do not use your data for marketing, profiling, or automated decision-making.

4. Legal Basis for Processing (GDPR)

If you are located in the EU or UK, our legal basis for processing your data is your consent (Article 6(1)(a) GDPR), given when you submit the contact form. You may withdraw consent at any time by contacting us.

5. How We Store Your Data

Inquiry data submitted via our contact form is stored securely on our hosting platform (Genspark/Hostinger infrastructure). Project-related communications are retained in secure email. We do not sell, rent, or share your personal data with any third parties except as required by law.

6. Data Retention

Inquiry data is retained for a maximum of 12 months from the date of submission, unless an ongoing project relationship exists. You may request deletion of your data at any time by emailing us.

7. International Data Transfers

Our practice is based in India. If you are in the EU or UK, your data may be transferred to and processed in India. We take reasonable steps to ensure your data is handled securely in accordance with this policy.

8. Your Rights

Depending on your location, you may have the right to:

  • Access the personal data we hold about you
  • Request correction of inaccurate data
  • Request deletion of your data
  • Withdraw consent at any time
  • Lodge a complaint with your local data protection authority

To exercise any of these rights, contact: arvindrthr0607@gmail.com

9. Changes to This Policy

We may update this Privacy Policy from time to time. The date at the top of this page will reflect the most recent revision. Continued use of this website after changes constitutes acceptance of the updated policy.

10. Contact

For any privacy-related questions: arvindrthr0607@gmail.com

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MedDev Advisory Medical Device Regulatory Consulting

Expert medical device regulatory consulting for ISO 10993 biological evaluation, EU MDR Technical File, FDA 510(k) documentation, and selected CDSCO support. Science-led. Regulation-ready.

Services

Biological Evaluation Plan Biological Evaluation Report Toxicological Risk Assessment ISO 10993-1:2025 Gap Analysis Material Change Assessment Notified Body Response EU MDR Support FDA 510(k) Support CDSCO Support

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Contact

arvindrthr0607@gmail.com
Kanpur, India
Response within 24 hours on business days

Information on this website is for general informational purposes and does not constitute legal, regulatory, or clinical advice. Services are provided based on client-supplied information and do not guarantee regulatory clearance, CE marking, or notified body/FDA outcomes. Results vary by device, evidence package, and regulatory pathway.

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