Compare & Book Regulatory Compliance Services in Minutes
Appoint a rep, book lab testing, or start a label review in minutes. Compare vetted regulatory service providers with instant pricing — charged only when your provider accepts.
Available services
- EU Authorized Representative (EC REP) – Medical Devices
- UK Responsible Person – Medical Devices (UKCA)
- Cosmetic Label Compliance Review & Fix
- Med Device Label + UDI Quick Check
- IFU / Label QA Proofread
- FDA U.S. Agent (Devices + Food + Cosmetics)
- Cosmetics Responsible Person (EU/UK)
- Swiss Authorized Representative (CH-REP)
- EU GDPR Representative (Art. 27)
- GDPR Quick Consultation
- GDPR Starter Gap Assessment
- Privacy Policy + Website GDPR Review
- Records of Processing / Basic Compliance Pack
- DSAR / Data Rights Process Setup
- DPA / Vendor Privacy Review
- EU GPSR Responsible Person
- WEEE / EPR Authorized Representative
- MoCRA Cosmetics: Facility Registration + Product Listing (US)
- EU CPNP Notification (Cosmetics)
- UK SCPN Notification (Cosmetics)
- MHRA Device Registration (UK)
- GUDID DI Submission (US)
- EUDAMED Actor / UDI Setup Support (EU)
- Cosmetic Claims Substantiation Review (Light)
- Artwork Release Package
- Translation Coordination + Linguistic QA
- CPSR Preparation (EU/UK)
- PIF Compilation & Hosting Support
- Formula + INCI Review
- SOP Pack (Starter QMS)
- Forms & Templates Pack
- Gap Assessment vs ISO 13485 / 21 CFR 820 (Light)
- Mock FDA Inspection (Remote) – Readiness Sprint
- Mock ISO 13485 Internal Audit (Remote)
- Form 483 Response Pack
- Warning Letter Response Support (Phase 1 Pack)
- Complaint Handling Process + SOPs
- Medical Device Biocompatibility Testing (ISO 10993)
- Cosmetic Product Testing (Lab)
- PMS / PMCF / PSUR Writing Support
- FDA MDR / EU Vigilance Reporting Support
- Recall / Field Action Readiness Checklist
