WELLNEST HEALTHCARE TECHNOLOGYCO., LIMITED

Doctor Mall是針對私營醫療市場打造的「智能診所中台」，同時連接線上和線下業務。通過接入平台，診所醫生和工作人員可以在「不改變現有工作模式」的情況下，迅速適應數字化轉型，並打通線上與線下業務。平台介面簡潔、系統操作簡單方便，系統更新與維護由公司統一負責，加上「先使用，後付費」的模式，讓診所可以實現「零成本數字化升級」。 Doctor Mall is an 'intelligent clinic platform' designed for the private healthcare market in the world, connecting both online and offline businesses.By integrating the platform, clinic doctors and staff can quickly adapt to digital transformation without changing their existing work modes, while bridging online and offline operations. The platform interface is simple, and the system operation is easy to use. System updates and maintenance are handled by the company, and with a 'use first, pay later' model, clinics can achieve'zero-cost digital upgrades.'   產品核心特點Core Product Features： 醫療版的SaaS 平台(Healthcare SaaS Platform)： Shopify+美團模式 —— 既提供診所數字化基建，又掌控終端流量入口。 Shopify + Meituan model — provides digital infrastructure for clinics while controlling the entry point for terminal traffic.  互聯網+AI技術(Internet + AI Technology)： 智能病歷記錄和個性化健康教育，遠程醫療可跨語言無障礙溝通，實現全球醫療覆蓋。 Smart medical record keeping and personalized health education. Remote medical services facilitate cross-language communication without barriers, achieving global healthcare coverage. 智慧醫療樞紐(Hong Kong-style Smart Healthcare Hub)： 同時連接線上與線下業務，實現「醫療問診+國際藥品採購」一站式服務。 Connects both online and offline services, offering a one-stop service for "Medical consultations + international drug procurement."  

 Medical PaaS System 

香港標準及檢定中心有限公司 (STC)

STC&#39;s Biocompatibility Testing services for medical devices includes:&nbsp; 	 Absorbent Incontinence Products &nbsp; &nbsp; 	 Adhesives &nbsp; &nbsp; &nbsp; &nbsp; &nbsp;&nbsp; 	 Blood Collection &amp; Storage Devices &nbsp; &nbsp; 	 Bone Void Fillers &nbsp; &nbsp; 	 Central Nervous System Implants 	 Combination Products &nbsp;&nbsp; 	 Contact Lenses &nbsp; &nbsp; &nbsp; 	 Dental Implants &nbsp; &nbsp;&nbsp; 	 Devices Containing Antimicrobials 	 Device Raw Materials 	 Hemodialysis Disposables 	 Implantable Drug Delivery Devices &nbsp; &nbsp; 	 Infusion / transfusion Devices&nbsp; 	 Intraocular Lenses&nbsp; 	 Laparoscopes &amp; Endoscopes &nbsp; &nbsp; 	 Ocular Implants 	 Orthodontic Devices 	 Orthopedic Implants 	 Ostomy Devices 	 Reusable Devices 	 Surgical Gloves 	 Sutures 	 Syringes 	 Urinary Stents 	 Urologic Catheters 	 Vascular Catheters 	 Vascular Grafts 	 Vascular Stents 	 Ventricular Assist Devices 	 Wound Drainage Devices 	 Wound Dressings&nbsp;    Cytotoxicity Study Test    (3 weeks lead time)  	 MTT Method&nbsp;(ISO 10993-5) 	 Agarose Overlay Method&nbsp;(ISO 10993-5 / USP 87) 	 Filter Diffusion Method&nbsp;(ISO 10993-5) 	 Direct Contact Method&nbsp;(ISO 10993-5 / USP 87) 	 MEM Method&nbsp;(USP 87)  
  Irritation &amp; Skin Sensitization Test   	 Skim Sensitization Study (GPMT / Closed-patch)&nbsp;(ISO 10993-10) (6 - 8 weeks) 	 Skin Irritation Test&nbsp;(ISO 10993-10) (3 weeks) 	 Intracutaneous (Intradermal) Reactivity Test&nbsp;(ISO 10993-10 / USP 88)&nbsp;(3 weeks) 	 Oral Mucosa Irritation Test&nbsp;(ISO 10993-10) (8 - 10 weeks) 	 Vaginal Irritation Test&nbsp;(ISO 10993-10) (8 - 10 weeks) 	 Penile Irritation Test&nbsp;(ISO 10993-10) (8 - 10 weeks) 	 Rectal Irritation Test&nbsp;(ISO 10993-10) (3 months) 	 Ocular Irritation Test&nbsp;(ISO 10993-10) (3 - 4 weeks)    Systemic Toxicity Test   	 Acute Systemic Toxicity Test&nbsp;(ISO 10993-11 / USP 88) (3 weeks) 	 Subacute Systemic Toxicity Test (14 days / 28 days)&nbsp;(ISO 10993-11) (6 or 8 weeks) 	 Subchronic Systemic Toxicity Test (90 days / 180 days)&nbsp;(ISO 10993-11) (5 or 8 months) 	 Pyrogen Test&nbsp;(ISO 10993-11) (3 weeks)  
  Local Effects after Implantation Test   &nbsp;  (ISO 10993-6) (at least 4 weeks)  	 Implantation in Subcutaneous Tissue Test 	 Implantation in Muscle Test&nbsp; 	 Implantation in Bone Test&nbsp;  
  Interactions with Blood Test    (2 weeks)  	 Hemolysis Test&nbsp;(ISO 10993-4 / GB) 	 Hemolysis Test&nbsp;(ASTM F756) 	 APTT、PT、TT、FIB&nbsp;(ISO 10993-4 / GB) 	 Platelet Count Test 	 Complement Test&nbsp;(ISO 10993-4 / GB) 	 Thrombosis Test&nbsp;(in Vivo / in Vitro)&nbsp;(ISO 10993-4 / GB)  
  Genotoxicity Test    (ISO 10993-3)  	 Ames Test&nbsp;(8 weeks) 	 Mouse Lymphoma Assay Test&nbsp;(10 weeks) 	 Chromosome Aberration Test &nbsp;(10 weeks)  If you have any further question, please feel free contact us at&nbsp; enquiry@stc.group &nbsp;or visit our website:&nbsp; https://www.stc.group/en/contact 

Biocompatibility Testing Services for Medical Devices

港芝製造有限公司

We provide EMS solution. Our service includes OEM, OBM and ODM manufacturing. Our product experience includes Medical and Healthcare Equipment, Electric Appliance Control Units, Hospital Equipment, Temperature Monitoring Devices, Deodorizer, Light Tube, Safety and Security Equipment, Assistive Hearing Devices, Communication Equipment, Pest Control Units, Currency Handling Devices and PCB Assemblies. Our existing manufacturing plant is in Dongguan, China. We will have a new plant in Vietnam starting for Production by January 2020 at Phase-1; the Phase-2 facilities will be scheduled completion by end 2020.

OEM / ODM / EMS Manufacturing

Information Processing Consultants Ltd

個人護理系統(PICS)是一套獲獎的軟件方案，專門為護老院舍及特殊院舍而編寫。IPc自2016年自主開發。在2017年推出。已在香港及澳門多所院舍安裝實施。並於2018年香港政府的ICT2018比賽中獲得銀獎。PICS主要有兩個模塊: 院舍行政護理及藥物行政。兩模組無縫結合，其主要目的是要提供一套完備的院舍系統使醫療事故可以避免。 院友于入院前會有入院前的評估。作好預先的準備。院舍行政護理包括院友的個人資料及醫療資料的錄入，從而針對院友個人生成的護理計劃(ICP)。ICP記錄了每一院友的維生指數，傷口位置，牙列及護理時間表。這時間表自動提醒照顧者該做的工作。例如，食藥、量血壓、血糖指數、血含氧指數、及脈搏。這些維生指數可以通過藍牙傳到PICS的資料庫。（藍牙設備需通過IPc的技術團隊認證）。 藥物行政包含在院藥房的庫存。院舍內的藥房按醫生(MO)處方配藥。在配藥的過程中，PICS會根據其資料庫提醒藥劑師這些藥物有沒有衝突而導致不良後果。護士及護理員用安卓(Android)平板電腦派藥。平板上有相關院友的相片並要派的藥物一比一的相片，達致三核五對的要求。派送了的藥物隨即場錄入PICS，成為院友用藥記錄(eMAR)。MAR是香港政府及澳門政府必須要求。 PICS帶一個駐院MO模塊用於即時記錄對院友的診斷及處方。處方即時發送到院內的藥房從而加速藥物配劑及減省MO的工作。 藥物管理可以擴展到自動包藥。藥劑是按每一時段為一獨立包裝。從而緩解護士在院舍的工作壓力。現時PICS可以與JVM及Yuyama包藥機無縫對接。 IPc擁有PICS的所有智慧財產權。若院舍有特殊要求，IPc可為其修改。 為推廣PICS在院舍的使用，現以軟體作為服務(SaaS)形式推出使一次性的投資減到最低。院舍祇需以月租就可以開始使用。這月租費用已含電腦伺服器及軟體，更省卻駐院的IT員工。 

安老院舍護理及藥劑行政管理

Founded in 1963, Hong Kong Standards and Testing Centre (STC) provides a wide range of professional testing services for proprietary Chinese medicine, Chinese Materia Medica, pharmaceutical products, food, microbiological quality and cosmetics, environmental testing as well as &quot;STC tested&quot; Mark Certification.

Chinese Medicine & Chinese Raw Herb testing

Medical device regulations are constantly changing and evolving to better safeguard the health and safety of the public. However these regular changes may impact manufacturers with regards to their product requirements and registrations with local and overseas regulators.
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At STC, our team of knowledgeable experts are up-to-date with the latest regulatory requirements in key markets to ensure that compliance is met and support medical device manufacturers in gaining market entry quickly.

Key Market Support: 	 Australia&nbsp;(DOH) 	 Brazil&nbsp;(MOH) 	 Canada&nbsp;(HC) 	 China&nbsp;(CFDA) 	 Europe&nbsp;(CE Notified Body MDD / MDR) 	 India&nbsp;(MOH) 	 Japan&nbsp;(MHLW) 	 Korea&nbsp;(MFDS) 	 Malaysia&nbsp;(MOH) 	 Singapore&nbsp;(HSA) 	 Taiwan&nbsp;(TFDA) 	 United States&nbsp;(FDA)   Our Medical Device Product Classification &amp; Regulatory Support services include : 	 Document Preparation for ISO13485 Certification (Gap Analysis) 	 Medical Grade Components Sourcing 	 Technical File / Dossier Compiling 	 Collateral, Particular Harmonized &amp; Industrial Standards Testing 	 Test Equipment Setup for Performance Testing 	 Biological Testing according to GLP Requirements 	 Submission of Technical File to Regulators 	 Representation by Local Representatives&nbsp; 	 License Holding &amp; Risk Management 	 On-site Support during Regulator Inspections 	 QMS/QSR support on CFR820, ISO13485, Canada MDR, Korea GMP, Brazil GMP and Japan Ordinance 169    &nbsp;Electrical Testing   	 ISO 17025 	 CB Scheme 	 NRTL Program.  
  Biological Testing&nbsp;(ISO 10993)   	 Interactions with blood&nbsp;(ISO 10993-4) 	 Vitro Cytotoxicity&nbsp;(ISO 10993-5) 	 Local Effects after Implantation&nbsp;(ISO 10993-6) 	 Ethylene oxide sterilization residuals&nbsp;(ISO 10993-7) 	 Irritation&nbsp;(ISO 10993-10) 	 Skin Sensitization&nbsp;(ISO 10993-10) 	 Systemic Toxicity&nbsp;(ISO 10993&nbsp;-11)   LUCIDEON Medical Device Services  	 As part of our commitment to offering the most extensive services to our customers, STC is working in collaboration with LUCIDEON to provide a greater range of services including Medical Device Consultancy, Materials Developments and Technology Innovations.&nbsp;  If you have any further question, please feel free contact us at&nbsp; enquiry@stc.group &nbsp;or visit our website:&nbsp; https://www.stc.group/en/contact 

Medical Devices Testing

Hong Kong Cancer Testing Center Limited

Multi-target Cytotoxic T Lymphocyte(MCTL®)Cancer Post-Treatment Follow-Up technology is an advanced precision medical solution integrating cancer detection and treatment. By analysing the type and quantity of tumour-specific antigens (tumour targets) in serum, we identify cancer development and determine positive targets for each individual. 

MCTL® Cancer Post-Treatment Follow-Up Test

大華金屬制作有限公司

Clear and eye-catching lightbox signages are the key visual elements for medical and health institutions to convey a professional image! It allows patients to identify the trusted institutions instantly on the signboard, and guiding those in need to actively seek professional help.  Brand:DAIWA Classification:Lightbox Signage Customised:YES Optional Materials:Stainless Steel, Aluminum, Copper, Iron, Acrylic; Metal surface:Painted; Brushed, Satin or Mirror Polished (Plating are available); LED Colors: Cool White6500K; Natural White4500K; Warm White3500K; Green; Blue; Yellow; Red; Pink. Plating Colors:Titanium Gold; Champagne Gold; Rose Gold; Black; Antique Brass; Antique Copper. Application: Indoor, outdoor, mainly for branding decoration and modern office. Application Industry:Catering, Hotel, Medical, Beauty, Banks, Retail and High-end Industry, etc.  - Premium Materials: We use only top-grade materials to ensure your sign lasts for years while staying bright and fresh. - Customized services: Our professionals will recommend the optimal solution according to your preferences. - Years of Expertise: With years of exquisite Hong Kong-style craftsmanship, we are your expert in sign customization. - Service Commitment: We provide exceptional service and treat everyone with honesty – that' s our core promise.            

3D Letters Lightbox Signage for Medical Industry

Founded in 1963, Hong Kong Standards and Testing Centre (STC) provides a wide range of professional testing services for proprietary Chinese medicine, Chinese Materia Medica, pharmaceutical products, food, microbiological quality and cosmetics, environmental testing as well as &quot;STC tested&quot; Mark Certification.


Svi Public Co Ltd

Electronic manufacturing service, start from PCBA to Final Assembly. Factories located in Thailand, Austria, Slovakia and Hungary. 	 Audio 	 Medical 	 Telecommunication 	 Industrial 	 Transportation 	 etc.,  

Electronic Manufacturing Service - Medical Product

STC&#39;s expertise in pharmaceutical testing can help ensure that products meet safety and quality requirements through evidence-based assay and identification methods along with toxicity assessments and stability testing in accordance to pharmacopeia&nbsp;(an official publication containing a list of medicinal drugs with their effects and directions for use).

STC&#39;s pharmaceutical testing service also extends to cover Chinese and herbal medicine testing. As an accredited laboratory, STC&rsquo;s testing capabilities include the full list of mandatory testing requirements for all proprietary Chinese medicine (pCm) stipulated by the&nbsp;Department of Health in Hong Kong&nbsp;to ensure safety and quality.

  Proprietary Chinese Medicine (pCm) Safety Testing   	 Pesticides Residues&nbsp;(e.g. Aldrin, Chlordane, DDT, Endrin, etc.) 	 Microbial Limit&nbsp;(e.g. total bacteria count, molds &amp; yeasts count, etc.) 	 Issuance of Summary Report on Product Safety Document    Product Quality &amp; Safety Testing   	 Assay and Identification of Active Ingredients in PCM 	 Microbial Limit&nbsp;(e.g. total bacteria count, molds &amp; yeasts count, etc.) 	 General Physical Testing&nbsp;(e.g. determination of water, disintegration test, filling, packing variation, size of granules, etc)    Toxicity &amp; Biocompatibility Assessment   	 Systemic Toxicity&nbsp;(Acute, Sub-Chronic, and Chronic) 	 Local Toxicity&nbsp;(Irritation and Skin Sensitization) 	 In-vitro Cytotoxicity 	 Genotoxicity, Carcinogenicity and Reproductive Toxicity    Pharmaceutical Adulterants Screening   	 Men&rsquo;s Drugs 	 Slimming Drugs 	 Steroids 	 Sex Hormones 	 Analgesic Drugs 	 Drugs for lowering blood pressure, cholesterol or sugar levels    Stability Testing   	 Conducted in General, Real-Time and Accelerated manner    Method Validation (Assay / Identification)   	 Applicable to known or characteristic constituents in finished products    Pharmacopeia Monograph   	 Compliance Testing stipulated in British, US, Japan, EU, and China Pharmacopeia monograph  If you have any further question, please feel free contact us at&nbsp; enquiry@stc.group &nbsp;or visit our website:&nbsp; https://www.stc.group/en/contact 

Pharmaceutical Testing

SmartAge Intelligence Limited

In the SmartAge Care Service, telenurses leverage SmartAge Home System's data and AI to pinpoint individual needs, offer triage services, and connect elderly individuals with appropriate community resources, thereby streamlining case management efficiency.  

SmartAge Telenursing 

Characterization for materials used in medical devices &ndash; an analysis of a material&rsquo;s composition, purity, uniformity, sterilant residuals and extractables &ndash; is an essential step to verify their suitability for human body contact, thus should not be missed out throughout the product life cycle.

Following the enforcement of&nbsp;RoHS&nbsp;2 in the European Union, which restricts the use of specified hazardous substances in electrical and electronic equipment, and medical devices are now added to the scope of the Directive and have to be verified as&nbsp;RoHS-compliant.

The chemical laboratory at STC is equipped with the most advanced testing equipment; our team of experts can perform material characterization and RoHS analysis with a wide range of testing methods. We can help manufacturers identify the appropriate testing program based on the intended use of a device and material, and its expected nature of contact with the human body.
&nbsp;  Material Characterization - Guidelines &amp; Standards   	 U.S. FDA Blue Book Memorandum GP#95-1 	 ISO 10993-1, &ldquo;Biological Evaluation of Medical Devices&rdquo; 	 ISO 10993-18, &ldquo;Chemical Characterization of Materials&rdquo; 	 FDA Guidance Document, &ldquo;Container Closure Systems for Packaging Human Drugs and Biologics&rdquo;&nbsp;&nbsp;&nbsp;    Material Characterization Testing Capabilities   	 Physiochemical Test 	 Fourier Transform Infrared Spectroscopy (FTIR) 	 High-Performance Liquid Chromatography/mass Spectrometry (HPLC-MS) 	 Gas Chromatography / Flame Ionization Detector (GC / FID) 	 Gas Chromatography / Mass Spectrometry (GC / MS) 	 Inductively Coupled Plasma Spectrometry (ICP) 	 Specific Gravity 	 Gel-Permeation Chromatography (GPC) 	 Viscosity 	 Differential Scanning Calorimetry (DSC)  If you have any further question, please feel free contact us at&nbsp; enquiry@stc.group &nbsp;or visit our website:&nbsp; https://www.stc.group/en/contact 

Chemical Testing for Medical Devices

STC offers Safety &amp; Performance Testing services for medical device products such as: 	 Electronic Clinical Thermometers 	 Infrared Thermometers 	 Electronic Sphygmomanometers 	 Electronic Laparoscopes 	 Electronic Endoscopes 	 Electrocardiographs 	 Multi-parameter Monitors 	 Pulse Oximeters 	 Therapeutic Lamps 	 Humidifiers 	 Nerve &amp; Muscle Stimulators 	 High-potential Therapeutic Apparatus 	 Electro-therapeutic Equipment 	 Magnetic Therapy Equipment 	 Hearing Aid&nbsp;  
  General Standard   	 General Requirements&nbsp;(EC / EN 60601-1)  
  Collateral Standards   	 Usability&nbsp;(IEC / EN 60601-1-6; IEC / EN 62366) 	 Alarm System&nbsp;(IEC / EN 60601-1-8) 	 Medical Electrical Equipment for Home Healthcare&nbsp;(IEC / EN 60601-1-11)  
  Particular Requirements   	 Nerve &amp; Muscle Stimulators&nbsp;(IEC / EN 60601-2-10) 	 ECG Related Equipment&nbsp;(IEC / EN 60601-2-25; IEC/EN 60601-2-27; IEC / EN 60601-2-47) 	 Sphygmomanometers&nbsp;(IEC / EN 80601-2-30; IEC/EN 60601-2-34; ISO / EN ISO 81060-1) 	 Multi-parameter Monitors&nbsp;(IEC / EN 60601-2-49) 	 Thermometers&nbsp;(ISO / EN ISO 80601-2-56) 	 Light Source Equipment (IEC / EN 60601-2-22; IEC / EN 60601-2-57) 	 Pulse Oximeters&nbsp;(ISO / EN ISO 80601-2-61) 	 Hearing Aids&nbsp;(IEC / EN 60601-2-66) 	 Additional Requirements&nbsp;(IEC / EN 60601-2-XX; IEC / EN 80601-2-XX, ISO / EN ISO 80601-2-XX; ISO / EN ISO XXXX)  If you have any further question, please feel free contact us at&nbsp; enquiry@stc.group &nbsp;or visit our website:&nbsp; https://www.stc.group/en/contact 

Safety and Performance Testing Services for Medical Device Products

We offer &quot;STC&quot; tested mark certification services for customers. It is covered on food, health supplements, proprietary Chinese medicine, cosmetics and toiletry products. Our services are professional and reliable.
 
  &quot;STC&quot; tested mark certification. 
  Covered on food, health supplements, proprietary Chinese medicine, cosmetics and toiletry products. 
 

Certification Service

Oxygen Two Point Zero Company Limited.

 Award-winning websites for medical manufacturers and healthcare organisations. We build B2B and B2C websites on HubSpot, built for international search visibility and designed to convert g lobal buyer interest into revenue. Bilingual capability. ISO 27001 certified. Built for medical companies who need a digital presence that grows their business.  

Medical Websites

CMA檢定中心

我們為香港衛生署認可提供中成藥註冊服務的實驗室，提供安全性、穩定性測試及分析方法驗證。本中心的實驗室更為中藥材的天麻顯微鑒別、灰分測試和水分含量取得香港實驗所認可計劃 (HOKLAS)認可，並同時將認可的中藥測試類別中的重金屬測試範圍擴展到檢測中成藥和中藥材的銅含量測試。 中成藥安全性測試 重金屬及有毒元素含量微生物限度農藥殘留量品質及穩定性測試 中藥標準物含量測試加速穩定性測試實時穩定測試中藥掺雜西藥成分 掺雜西藥測試中藥材品質測試 為中藥材天麻進行含量測定，指紋圖譜，色譜，顯微鑒別為中藥材進行灰分，水分含量，重金屬，酸不容性灰分，黴菌毒素測試 精於投資精良的設備，並集合專業團隊，廠商會檢定中心提供藥物測試包括中醫和西藥，以確保藥物的品質和安全。我們誠意為您提供諮詢服務，技術方案和培訓。 

中成藥測試

The proprietary Chinese medicine testing services are carried out by the renowned Hong Kong Standards and Testing Centre (STC). Services include heavy metals and toxic elements, method validation, microbial limits, pesticide residues and more, ensure the distribution of the best-quality proprietary Chinese medicine&nbsp;to the market.&nbsp; 	 Heavy metals and toxic elements. 	 Method validation. 	 Microbial limits. 	 Pesticides residues. 	 Pharmaceutical adulteration screening.  

Proprietary Chinese Medicine Testing

STC offer&nbsp;Electromagnetic Compatibility (EMC) Testing services for medical devices such as:&nbsp; 	 Medical Electrical Equipment 	 In Vitro Diagnosis (IVD) Medical Equipment&nbsp;    Electromagnetic Compatibility Testing (EMC)   	 IEC / EN 60601-1-2 	 CISPR 11 / EN 55011 	 IEC / EN 61326-1 	 IEC / EN 61326-2-6 	 FCC Part 15 / Part 18 	 ICES-001 / ICES-003  
  Radio Frequency Testing (RF)   	 EN 300330-1; EN 300330-2 (9 kHz to 30 MHz) 	 EN 300220-1; EN 300220-2 (25 MHz to 1000 MHz) 	 EN 300440-1; EN 300440-2 (1 GHz to 40 GHz) 	 FCC Part 15 / Part 18; RSS-210&nbsp;    Bluetooth   	 EN 300328 (2.4 GHz) 	 FCC Part 15 / Part 18 	 RSS-247    Wi-Fi   	 EN 300328 (2.4 GHz TRx WiFi b / g / n) 	 EN 301893 (5.8 GHz) 	 FCC Part 15 / Part 18 	 RSS-247  If you have any further question, please feel free contact us at&nbsp; enquiry@stc.group&nbsp; or visit our website:&nbsp; https://www.stc.group/en/contact 
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Electromagnetic Compatibility for Medical Devices

Based on the world’s largest tumor drug target database, AKJ™ detects tumour-specific targets in serum to identify the presence of cancer cells, enabling cancer early screening. 

AKJ™

廣州威綽商品檢測技術服務有限公司

 	 Some tests should be done in the professional laboratory instead of testing at the factory because of accuracy or special testing types of equipment required. 	 As a leading inspection service supplier in China, V-Trust has a long-term cooperative relationship with many accredited laboratories, so we can provide you with more competitive prices and professional testing arrangement. V-Trust can efficiently manage the testing of samples in liaison with qualified and accredited laboratories when you need formal certification or professional test. 	 We can go to the factory and select samples randomly on site instead of letting the factory choose them. We can select the best laboratories, based on price and lead-time, for each type of test or certification, such as Oeko-Tex 100, AZO dyes, Fastness, etc.  

Lab Testing and Certification

This lab testing service is carried out by a group of professionals for added effectiveness. The advanced machines and technologies used help guarantee added accuracy. This lab testing is compatible with CPSIA, REACH, CE and RoHS certifications. 	 Efficient and reliable. 	 With excellent after-sales supports.  

Lab Testing

CMA Testing提供美國，歐洲和亞洲市場原材料和口罩測試及諮詢服務。我們全面支持製造商和進口商從原材料質量控製到個人護理產品的檢驗。 材料-熔噴無紡布 /熔噴布： ASTM F2100 / EN 14683 呼吸時的壓力差 (Delta P) (mm H₂O/cm²)對亞微米級微粒的過濾效率 (％)玻璃纖維檢測EN 12586 甲醛檢測其他 拉伸斷裂強度和斷裂伸長率偶氮染料環氧乙烷殘殘留量微生物檢測口罩-外科口罩： ASTM F2100 對細菌的過濾效率 (BFE) (％)呼吸時的壓力差 (mm H₂O/cm²)對亞微米級微粒的過濾效率 (％)抗模擬血液穿透效能 (mmHg)EN 14683 對細菌的過濾效率 (BFE) (％)呼吸時的壓力差 (Delta P) (Pa/cm²)耐濺性 (kPa)微生物清潔度 (CFU/g)AS 4381 對細菌的過濾效率 (BFE) (％)呼吸時的壓力差 (Delta P) (mm H₂O/cm²)抗模擬血液穿透效能 (mmHg)口罩-織物口罩/ DIY阻隔性口罩： 這是法國標準協會針對非醫用織物口罩制定的指南。 AFNOR SPEC S76 外觀檢查和尺寸檢驗包裝和材料檢驗標記和標籤檢驗清潔和乾燥度檢驗呼吸阻力（呼吸能力）檢驗及抗穿透性（顆粒過濾）檢驗呼吸面罩： 呼吸面罩的要求比外科口罩要復雜得多。 雖然兩者在標準，過濾效率，壓力差等之間有共同的參數，但是其他測試於不同國家有不同的參數來衡量其性能。 請從我們的白皮書中找到以下國家/地區標準和性能測試的詳細信息： https://www.cmatesting.org/news/featured-articles/white-paper-011/white-paper-011---respirator-standard_eng.pdf 國家標準美國42 CFR 84歐洲EN 149中國GB 2626澳洲 / 新西蘭AN/NZ 1716韓國KMOEL – 2017 - 64日本JMHLW Notification 214

個人護理

GRG METROLOGY & TEST GROUP CO., LTD.

GRGTEST has invested in and holding shares of Shenzhen Bolinda and Manhage, achieving the full coverage of inorganic and organic reference material products in fields including food, environment, clinical medicine and industrial products, and independently developed more than 200,000 types of reference materials and consumables. Reference MaterialsProficiency Testing and Quality Control SamplesSample Pretreatment Consumables and Chromatographic Columns

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