Comprendre le dossier technique étranger
Identify the actual product boundaries from manuals, specifications, software controls, accessories, and test records—not through language translation alone.
BEAUTY TECHNOLOGY COMPLIANCE
美容设备合规产品工程
从产品属性判断，到研发重构、实验验证与市场准入。基本定律帮助企业建立与真实产品一致、能够持续执行的合规路径。
Imported microcurrent NMPA case work
Ultrasound and ion-air projects in progress
Domestic microcurrent project in progress
SELECT YOUR STARTING POINT
Different companies face different challenges. Choose the entry point closest to your current stage.
01 / IMPORT TO CHINA
Fabricants étrangers et représentants en Chine
For products already marketed overseas and planned for China: determine regulatory status, rebuild Chinese materials, and establish an NMPA classification path.
Voir le parcours Chine des appareils importés 02 / DOMESTIC R&DR&D et fabricants en Chine
For products at concept, prototype, or redesign stage: confirm that functions and parameters match the intended regulatory route before testing and mass production.
Diagnostic réglementaire en phase de R&D 03 / MARKET CONTINUITYProduits commercialisés et marques
For marketed products: maintain consistency across instructions, product updates, partner training, and distributor promotion.
Voir la conformité post-commercialisation
IMPORT DEVICE COMPLIANCE
01
02
03
Les appareils importés constituent l’un des principaux domaines d’expertise de Basic Law.
The main challenge is not only the applicant or authorization documents, but whether the overseas product definition can be translated into a product logic that Chinese regulators can understand, verify, and consistently implement.
Construire la version Chine
Reorganize the product name, intended purpose, operating principle, parameter ranges, risk controls, and Chinese instructions according to China’s classification logic.
Piloter les projets de longue durée
Use the project platform to manage document versions, supplementary questions, verification tasks, client approvals, and regulatory communications.
OVERSEAS PRODUCTCHINA MARKET
TECHNICAL DOSSIEROverseas Technical DossierManual · Specification · Test
REGULATORY TRANSLATION
01Définition produitName / Intended use
02Système de preuvesRisk / Verification
03Parcours de classificationNMPA / Market entry
04Cohérence commercialeLabel / Marketing
REPRESENTATIVE PRACTICE
Projets représentatifs
Public cases illustrate project types and methods. Completed and ongoing projects are clearly identified, and no single case replaces an independent assessment of a specific product.
RF
不作为医疗器械管理
MC
不作为医疗器械管理
LED
不作为医疗器械管理
PHASED ENGAGEMENT
Décider par étapes et maîtriser l’investissement initial.
Complex devices should not enter a full submission process before sufficient information is available. Our staged approach provides a clear conclusion at each key decision point.
Vérification de la disponibilité du dossier
Confirm whether the available product information supports an assessment, identify material gaps, and determine whether formal technical diagnosis is required.
Reduce ineffective communication and false startsDiagnostic réglementaire formel
Define regulatory-status risks, adjustment directions, evidence needs, project duration, and the scope of subsequent work for management decision-making.
Proceed based on a clear conclusionReconstruction produit et soumission
Once the route is viable, proceed with product reconstruction, verification, classification, and market-consistency management.
Invest only in an executable pathÀ propos des honoraires
Fees depend on the technology, dossier completeness, product redesign, verification needs, importing entity, and submission level. Fees reflect professional judgment, product reconstruction, evidence development, and long-cycle project management—not document count. Scope, deliverables, and payment milestones are confirmed before formal engagement.
PROFESSIONAL SERVICES
Une chaîne complète de services pour l’accès au marché
China compliance for imported devices is a priority practice. Domestic projects proceed in stages from path diagnosis and product reconstruction to classification.
前期评估
Regulatory Pathway Assessment
从预期用途、作用原理、输出参数、人体接触方式和使用场景出发，识别产品进入医疗器械或非医疗器械路径的关键条件。
Voir le périmètre Services principauxReconstruction de la conformité produit
围绕名称、预期用途、功能组合、输出参数、说明书、风险控制和实验体系，对产品进行真实、可执行的合规调整。
Voir le périmètre 申报管理分类界定申报
围绕产品用途、原理、参数、风险和验证资料构建分类界定申报体系，并协助完成补充资料和项目沟通。
Voir le périmètre Conformité continue上市后年度合规
持续审查说明书、电商页面、招商材料、培训话术和产品升级内容，保持实际产品、认定资料和市场宣传一致。
Voir le périmètre Service prioritaire 国际业务美容设备进口与出口路径
提供进口美容设备中国属性认定、欧盟 MDR Annex XVI 边界判断、美国低风险健康产品初评及多市场产品定义。
Voir le périmètre
BASIC LAW METHOD
Toute conclusion réglementaire doit pouvoir être reliée au produit réel.
We place intended purpose, mechanism of action, technical parameters, risk controls, verification, and commercial operation within one coherent logic. Any inconsistency becomes a future project risk.
01
Définir la destinationConfirm target users, use settings, and non-medical purpose.
02
Expliquer le mécanismeIdentify the primary action and possible physiological effects.
03
Définir les limites techniquesVerify frequency, current, energy, temperature, pressure, and time.
04
Maîtriser les risquesImplement structural, software, operational, and warning controls.
05
Construire les preuvesSupport the product definition and submission rationale with verification evidence.
06
Maintenir la cohérenceAlign instructions, training, e-commerce content, and product updates.
CORE EXPERTISE
Expertise pour les produits aux mécanismes complexes
Our project work currently covers imported and domestic microcurrent devices, ultrasound and ion-air technologies, while continuing to develop evidence methods for radiofrequency, light-based, delivery and combination devices.
能量型设备
Radiofrequency Beauty Devices
重点处理射频能量输出、皮肤温升、作用机制、使用场景和医疗化宣称之间的关系。
- 频率与波形
- 输出功率与能量
- 皮肤温升和作用深度
电刺激设备
微电流与EMS设备
围绕微电流、脉冲电流、肌肉刺激和皮肤护理用途，建立产品参数与预期用途的一致性。
- 电流强度与电压
- 频率和脉冲波形
- 电极接触方式
导入型设备
超声与美容导入设备
处理超声频率、声强、接触介质、导入用途和组织作用之间的产品定义问题。
- 超声频率与声强
- 空化和热效应
- 接触介质
Light-based Devices
Light-based Beauty Devices
处理LED、宽谱光及其他光类美容设备的能量、温升、皮肤反应和用途边界。
- 波长与光谱
- 能量密度
- 照射距离和时间
透皮导入设备
Electroporation and Pneumatic-delivery Devices
围绕电脉冲、气压喷射、耗材液体和皮肤接触方式，判断导入设备的真实作用与监管路径。
- 电脉冲或气压参数
- 皮肤完整性
- 使用液体和耗材
组合型设备
Combination Beauty Devices
针对射频、微电流、超声、光、冷热、负压和振动等多功能组合设备进行系统判断。
- 主作用机制
- 功能独立或联动
- 最不利参数组合
COMPLIANCE INSIGHTS
Tout afficher
Analyses réglementaires pour la direction et la R&D
Translate regulatory changes, product mechanisms, and project experience into clear information for project initiation, redesign, budgeting, and market-entry decisions.
01DirectionPath and investment decisions
02R&DParameter and evidence boundaries
03MarketingClaims and operational consistency