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Report an Adverse Event

how to report

Use this form to report a side effect, allergic reaction, or product issue with any ViaDerma product. Submissions are reviewed by our regulatory team and reported to the FDA where required by law.

Privacy notice — Protected Health Information

Information you provide may include Protected Health Information under HIPAA. It is collected solely for adverse event evaluation and reporting to the FDA under 45 CFR §164.512(b). Encrypted in transit and at rest, restricted access, retained for 6 years. When submitted to the FDA, the patient is identified by a code (e.g., initials), not by name.

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Section 1 of 7

Product information

Product information

Section 2 of 7

Reporter information

Reporter information

Section 3 of 7

Patient information

Patient information

Section 4 of 7

Adverse event details

Adverse event details

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Learn more on a call with a specialist

Schedule a free consultation with our sales team representative and discover how ViaDerma can bring innovation into your medical facility

About Us CTA Image

Learn more on a call with a specialist

Schedule a free consultation with our sales team representative and discover how ViaDerma can bring innovation into your medical facility

About Us CTA Image

Learn more on a call with a specialist

Schedule a free consultation with our sales team representative and discover how ViaDerma can bring innovation into your medical facility