Enterprise Consultation & Audit Requests
If you are an international importer, medical distributor, or brand compliance officer seeking verification of manufacturing standards, please utilize this portal to contact our regulatory team.
Qualified enterprise entities may request access to comprehensive factory audit checklists, cleanroom verification data, and technical dossier summaries.
📬 Contact Channels
- Official Inquiry Email:
info@aesthetic-regulatory.com(Please allow 24–48 hours for our regulatory affairs team to review your technical brief.) - Regulatory Liaison Office:Global Aesthetic Regulatory Compliance Group (ARCG)Technical Standards Division
📝 Request Formal Access
(Tip for Webmaster: You can insert a standard Contact Form 7 / Fluent Forms below with the following fields)
- Full Name / Title
- Corporate Email (Free webmails like Gmail/Yahoo may require additional verification)
- Company Name & Website
- Target Market (US FDA / EU MDR / AU TGA / Other)
- Inquiry Type:
- Request Factory Audit Report Summary
- Verify Material Biocompatibility Data ($ISO\ 10993$)
- OEM/ODM Compliance Consultation
- General Regulatory Inquiry