Certifications That Clear Vendor Review

RV Pharma programs run under documented quality controls from raw material receipt through batch release, with paperwork ready for your compliance team.

Request the Compliance Packet View Sample COA

Our Standards

Four Things Your Vendor Review Will Ask For

Registration

FDA-Registered Facility

Facility registration documentation is included in the compliance packet provided to qualified accounts.

21 CFR 111

cGMP Compliant

Programs run under current Good Manufacturing Practice controls for dietary supplements, from raw material receipt through batch release.

Certificate

NSF/ANSI 455-2

Certified to the NSF/ANSI 455-2 Good Manufacturing Practices standard for dietary supplements. A certificate copy is in the compliance packet.

Per Lot

Third-Party Tested

Independent laboratories verify actives, heavy metals, and microbiological limits on a lot-specific basis before release.

Compliance Packet

What’s in the Packet

Qualified accounts receive one packet with everything a vendor-onboarding or category team typically asks for.

✓cGMP compliance documentation
✓NSF/ANSI 455-2 certificate copy
✓FDA facility registration documentation
✓Lot-specific certificates of analysis
✓Product specification sheets per SKU
✓Certificate of insurance naming your company (on request)

Request the Packet

See the Format

Sample Certificate of Analysis

Every lot ships with a COA. Our redacted sample shows the layout, the tests run, and the release limits so your QA team knows what to expect.

Open the Sample COA

Need Documents for a Vendor Setup?

Tell us the retailer or platform you’re onboarding with and we’ll send the paperwork that matches their checklist.

Request the Compliance Packet Buyer Resources