PRODUCT
Product Authenticity
Product structure, functions, parameters, and use must remain consistent with the submitted dossier.
ABOUT BASIC LAW
Turn the technical facts of complex products intoproduct definitions that regulators can understand and verify.
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.
01Import to China
02Product Reconstruction
03Classification
04Ongoing Compliance
OUR POSITION
Our professional methodology began with a long-running, complex imported microcurrent project.
That work confirmed that the real challenge is not submission itself, but translating overseas technical facts into product logic that the Chinese regulatory system can understand.
Existing overseas instructions, test records, and market positioning cannot simply be carried into China. Names, purposes, parameters, software, accessories, testing, and market claims must be realigned within the Chinese regulatory context.
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.
EVIDENCE
Complete Evidence
Risk controls and verification evidence must support the product definition rather than exist as disconnected reports.
MARKET
Commercial Consistency
Instructions, training, e-commerce, distribution materials, and dealer claims must follow the same compliance logic.
WHAT WE SOLVE
We address the systemic breaks that arise when products cross technology, regulation, and market operation.
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.
01IMPORT TO CHINA
China Regulatory Pathway for Imported Devices
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.
02PRODUCT REBUILD
Product Compliance Reconstruction
Build an executable product version around the name, intended purpose, function set, output parameters, operating logic, and risk controls.
- Functional and Parameter Boundaries
- Instructions and Use Logic
- R&D Version Consistency
03EVIDENCE SYSTEM
Evidence and Submission System
Organise risk identification, verification objectives, test plans, and classification arguments into a mutually supporting evidence chain.
04MARKET CONTINUITY
Ongoing Post-market Consistency Management
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.
BASIC LAW METHOD
Build a six-step compliance programme from the real product.
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.
Intended Purpose
Confirm target users, use settings, and non-medical purpose.
Mechanism of Action
Identify the principal mechanisms and possible physiological effects.
Technical Parameters
Define boundaries for frequency, current, energy, temperature, pressure, and duration.
Risk Control
Implement structural, software, operational, and warning controls.
Verification Testing
Support the product definition with safety and intended-purpose evidence.
Maintain Consistency
Align submissions, instructions, training, e-commerce, and version updates.
WORKING PRINCIPLES
Clear professional boundaries are the foundation of a sustainable long-term project.
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.
Keep Product and Dossier Consistent
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.
Assessment Before Project Commitment
Before a complex device enters a full project, its dossier, mechanism, and pathway feasibility should be assessed.
Each Project Stage Has Independent Value
Product reconstruction, test design, dossier systems, and project management each produce confirmable professional deliverables; value is not reduced to the final administrative outcome.
Determination Is Not the End
Product upgrades, sales claims, and distributor conduct must remain consistent with the determination dossier.
PROJECT OVERVIEW
In ProgressCompliance Project Management
Current MilestoneSubmission Dossier Confirmation
Project Progress68%
Action Items02
Dossier CollectionProduct ReconstructionVerification TestingClassification Submission
Technical Parameter ConfirmationCompletedIntended Purpose ConfirmationIn ProgressAdditional Verification RecordsPending
Client-Visible FilesProject Work Plan.pdfDossier Confirmation Checklist.docx
COMPLIANCE OPERATING SYSTEM
Turn professional judgment into a traceable project process.
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.
01Project stage and current milestone
02Client tasks and document uploads
03File versions and approval records
04Result delivery and annual management
Open Compliance Center
WORK WITH BASIC LAW
Obtain a decision-ready path assessment before committing to the full project cost.
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.
Basic LawRegulatory and Product Compliance for Imported and Domestic Beauty Devices
- Company
- Basic Law (Beijing) Brand Management Co., Ltd.
- Telephone
- 189 1026 3383
- zuo.basiclaw@outlook.com
- Address
- Beijing Economic-Technological Development Area, Beijing, China