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

프로젝트 계속하기

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.

서비스 선택

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
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Recommended

고객 포털

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

고객 포털 열기
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신규 프로젝트

제품 규정 준수 평가 신청

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.

개별 프로젝트 조회
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OEM Cooperation

비의료 규정 준수 OEM 제품 시장

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

OEM 시장 열기
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.

서비스 절차

1

자료 제출

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

2

프로젝트 평가

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

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진행 상황 확인

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.