Basic Law Compliance Portal

Basic Law Compliance Center

Product compliance assessment, formal project tracking, document submission, and deliverable access for business clients.

Product Compliance Medical Device Compliance Project Progress Management Client Document Center
Client Access
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Assessment / Client Portal / Lookup / OEM
COMPLIANCE WORKSPACE

Projekt fortsetzen

Assessment, Market, and Account are available in the bottom navigation. The home page keeps only the most frequent actions.

Use the bottom navigation for new-device assessment, the OEM market, and your account.

Service auswählen

Choose the module that matches your needs. Clients with multiple projects should use the Client Portal; private-label enquiries can use the OEM Market.

Long-term client tracking is prioritised
01
Recommended

Kundenportal

Sign in with the registered phone number and its last four digits. The system links all eligible projects under that number.

Kundenportal öffnen
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Neues Projekt

Antrag auf Produkt-Compliance-Prüfung

For a first enquiry, submit company, product, and device information. The team will conduct an initial review based on purpose, structure, parameters, and claims.

Start a Product Compliance Assessment
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Alternative Access

Single-project Progress Lookup

For a first-time or occasional lookup, use the project number and the last four digits of the registered phone number to view progress, outstanding documents, deliverables and project notices.

Ein Projekt abfragen
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OEM Cooperation

OEM-Markt für nichtmedizinische Compliance-Produkte

Explore OEM/ODM opportunities for beauty devices with a compliance foundation. A consultant will review consistency and risk after your enquiry.

OEM-Markt öffnen
Multiple ProjectsOpen the Client Portal to view all projects in one place.
New Product EnquirySubmit product information for an initial compliance assessment.
One Project OnlyUse the project number and last four digits of the registered phone number.
Find Private-Label ProductsOpen the OEM Market and submit a private-label enquiry.

Ablauf

1

Unterlagen einreichen

The client submits company, product, purpose, parameter, and available document information.

2

Projektprüfung

The team reviews the regulatory path, dossier readiness, and compliance risks.

3

Fortschritt verfolgen

The client tracks milestones, submits additional documents, and accesses deliverables.

Typical Scenarios

Non-medical Aesthetic Device Cross-border Device Compliance Non-medical Device Status Assessment Preliminary MDR / Annex XVI Assessment Document Submission and Project Tracking Client Deliverables

This page is a client-service entry point. Scope, deliverables, and conclusions are governed by the agreed service proposal and formal documents.