Product Authenticity
제품 구조, 기능, 파라미터 및 사용 방법은 제출 자료와 일치해야 합니다.
Basic Law focuses on China regulatory pathways and product compliance for imported and domestic beauty devices. Starting from overseas technical dossiers or domestic R&D versions, we organise intended purpose, mechanism of action, technical parameters, risk controls, verification evidence and market operation into an executable product system.
이 프로젝트를 통해 진정한 어려움은 제출 자체가 아니라 해외 기술 사실을 중국 규제 체계가 이해할 수 있는 제품 논리로 전환하는 데 있다는 점을 확인했습니다.
해외 설명서, 시험 자료, 시장 포지셔닝을 그대로 중국에 적용할 수는 없습니다. 명칭, 용도, 파라미터, 소프트웨어, 부속품, 시험 및 시장 표현을 중국 규제 맥락에서 다시 정렬해야 합니다.
Basic Law has since applied the same method to domestic microcurrent, ultrasound, ion-air, radiofrequency, and light-based devices: understand the product before choosing the path, establish evidence before organising the submission, and keep R&D, importation, instructions, and market operation aligned.
제품 구조, 기능, 파라미터 및 사용 방법은 제출 자료와 일치해야 합니다.
위험 관리와 실험 검증은 제품 정의를 뒷받침해야 하며 개별 보고서를 단순히 쌓는 방식이어서는 안 됩니다.
설명서, 교육, 전자상거래, 유통 모집 및 대리점 홍보는 동일한 규정 준수 논리를 유지해야 합니다.
For imported devices, these breaks often occur between overseas dossiers and China-specific definitions. For domestic devices, they often occur between R&D versions, submission materials, and sales claims.
Review overseas technical documentation, the actual product, and the China market plan to establish the China product name, intended purpose, evidence system, and classification pathway.
Build an executable product version around the name, intended purpose, function set, output parameters, operating logic, and risk controls.
Organise risk identification, verification objectives, test plans, and classification arguments into a mutually supporting evidence chain.
A determination is not the end point. Product upgrades, training materials, e-commerce pages, livestream scripts, and distributor claims can all change how the product is actually presented in the market.
Each step answers a specific question and provides verifiable input for the next, preventing R&D, submission, and sales teams from creating different versions of the product.
Confirm target users, use settings, and non-medical purpose.
Identify the principal mechanisms and possible physiological effects.
Define boundaries for frequency, current, energy, temperature, pressure, and duration.
Implement structural, software, operational, and warning controls.
Support the product definition with safety and intended-purpose evidence.
Align submissions, instructions, training, e-commerce, and version updates.
We do not trade lower fees or simplified judgement for project volume. We protect client investment through staged assessment, defined deliverables, and consistency with the real product.
Our goal is not to change product status through wording, but to build a compliance pathway supported by the actual product, verification evidence, and real market operation.
The target regulatory pathway must be based on the real product definition and risk controls. Formal documentation must match the product actually manufactured, imported, and sold.
Before a complex device enters a full project, its dossier, mechanism, and pathway feasibility should be assessed.
Product reconstruction, test design, dossier systems, and project management each produce confirmable professional deliverables; value is not reduced to the final administrative outcome.
Product upgrades, sales claims, and distributor conduct must remain consistent with the determination dossier.
Formal projects use the Basic Law Compliance Project Platform for progress, tasks, client documents, and file management. The platform turns complex work into confirmable stages, versions, and responsibility records while protecting internal review materials, submission strategy, and commercial information.
Submit instructions, technical parameters, operating principle, product images, and target market. A consultant will first confirm dossier readiness; projects requiring substantive technical judgement will proceed to a formal regulatory-path diagnosis with a defined scope.
