LANGUAGE
中文 EN
b35
CDMO+CRO+CSO
医疗器械一站式服务
CDMO+CRO+CSO One-stop
service for medical devices
WechatIMG205
2
The overall solution for pharmaceutical companies to transform into medical devices is to achieve effective and significant treatment through precise medication with precise numerical values
Drug resistance testing solution
Genetic testing solution
Drug metabolism testing solution
Individualized genetic testing solution
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Service Center
1
International registration/domestic NMPA registrat
China's NMPA registration, EU CE certification, US FDA certification and local product registration in other countries
2
Quality system management/counseling service
GMP quality inspection system consultation, IS013485 quality inspection system consultation, YY/T0287 quality inspection system consultation, production license, business license
3
Enterprise regulation training service
GMP quality inspection system consultation, IS013485 quality inspection system consultation, YY/T0287 quality inspection system consultation, production license, business license
4
Process improvement service
More than 15 years of production process improvement team to ensure mass production of products
5
Entrusted R&D services
The professional returned R&D team has forged the entrusted R&D of IVD, active and passive products in ten years
6
Clinical trial services
A professional clinical team of over 40 people provides you with clinical evaluation consulting services and clinical evaluation outsourcing services
7
Commissioned production service
Product manual, product technical requirements and process specifications, production process SOP, instrument SOP, raw material and product inspection standards
8
Process design and construction of clean workshop
Clean room standard, clean room layout, clean room building, air purification and purification air conditioning system, clean room utility design, clean room micro-vibration and noise control, clean room electrostatic and electromagnetic interference protection, clean room construction and installation, clean room inspection and certification, clean room operation management
9
Transformation of pharmaceutical enterprises
Drug resistance detection solutions Genetic testing solutions Drug metabolism detection solution Individualized genetic testing solution
10
Medical beauty product registration
Healing facial mask and anti HPV gel after Yimei laser surgery Commissioned production, registration, and research and development of Class II medical devices
Product Supermarket
In vitro diagnostic reagents
In vitro diagnostic reagents
Product Supermarket
Infusion/injection products
Infusion/injection products
Product Supermarket
Endoscope field
Endoscope field
Product Supermarket
Medical catheter consumables
Medical catheter consumables
Product Supermarket
In vitro diagnostic reagents and instruments
In vitro diagnostic reagents and instruments
About RAS

Guangdong Les Medical Technology Co., Ltd. is a one-stop medical device service platform in the mode of "CDMO+CRO+CSO", aiming to help the development of the medical device industry and accelerate the research and development, clinical, registration, production and sales of medical device products.


The Leis Medical one-stop service platform is committed to providing customers with one-stop services such as the system, research and development, clinical, registration and production of active, passive and IVD products, and providing all-round personalized solutions from product incubation to pre-marketing. Assist the transformation of pharmaceutical dealers, raw material manufacturers and pharmaceutical enterprises, the transformation of medical industry, the landing of scientific research institutions, and the optimization and upgrading of enterprise products.


6600
㎡
Production pilot site
2.1w
㎡
Clean workshop base for mass production
6w
㎡
Transformation park
30
species
Product coverage
240
people
Team size
60+
home
Cooperative enterprises
News
Company News
Major events
Exhibition information
11-14
2023
新版立卷审查要求更好助力医疗器械上市审评
11-14
2023
推动高新区工业经济高质量发展——访包头稀土高新区党工委委员、管委会副主任张强
11-14
2023
泰安高新区输变电装备及电线电缆产业链：6家企业通过泰安市研发机构建设备案
11-14
2023
战“疫”家庭“三原色” ——记怀化高新区坚守在抗疫路上的陈雨萌家庭
11-14
2023
肇庆高新区: 发挥知识产权强劲优势 服务企业创新迸发大能量
11-14
2023
西安高新区创业园优秀企业及项目巡礼
12-07
2023
共话政企合作 聚力产业发展丨徕斯医疗欢迎奉新县领导组莅临调研交流
8 月 2 日 下午，江西省宜春市奉新县领导组莅临我司进行医疗器械产业的调研和交流，本次交流座谈会在广州市黄埔区徕斯医疗会议中心召开，奉新县市场监督管理局局长魏国生、奉新县工业和信息化局局长杨斌、奉新县市场监督管理局副局长华劲勇、奉新县农牧渔场党委书记邹友富、广东省徕斯医疗科技有限公司联合创始人马莉娜、广东省徕斯医疗科技有限公司市场总监黄新荣及多方相关人员共同出席本次会议。
07-12
2023
徕斯医疗丨诚邀您参加2023年中国（北京）国际健康产业跨境博览会
尊敬的各位业内同仁，感谢您一直以来对徕斯医疗的信任与肯定，我们将于7月11日至13日在中国国际展览中心(静安庄馆)参加2023年中国（北京）国际生命健康产业跨境博览会，届时徕斯医疗将为各位到场嘉宾提供专业的医疗器械海外业务解决方案。期待您的光临！
07-12
2023
共话政企合作 聚力产业发展丨徕斯医疗欢迎常德市武陵区领导组莅临考察交流
6 月 1 日 上午，常德市美妆产业园项目合作交流座谈会在广州市黄埔区徕斯医疗会议中心召开，常德市武陵区人大常委会主任曹慧、武陵区人民政府副区长徐杰、武陵区市场监督管理局局长戴正伟、广东省徕斯医疗科技有限公司联合创始人马莉娜、广东省徕斯医疗科技有限公司市场总监黄新荣、广州众成大数据科技有限公司董事长周勇及多方相关人员共同出席本次交流座谈会。
07-12
2023
徕斯医疗丨第87届中国国际医疗器械（春季）博览会（CMEF）精彩回顾！
通过本次参展，徕斯医疗获得了众多观展嘉宾的青睐和认可，提高了徕斯品牌CDMO+CRO+CSO一站式服务在行业内的市场价值，同时也挖掘出大量的意向客户和潜在客户。
07-12
2023
徕斯医疗丨您有一份来自上海CMEF的邀请函待查收！
尊敬的各位业内同仁，感谢您一直以来对徕斯医疗的信任与肯定，我们将于5月14日至17日在国家会展中心（上海）参加第87届中国国际医疗器械（春季）博览会（CMEF），届时徕斯医疗将为各位到场嘉宾提供专业的医疗器械整体服务解决方案，期待您的光临！
07-12
2023
徕斯医疗亮相生物岛“企业高管面对面”大咖沙龙活动，助力医疗器械CXO产业蓬勃发展
徕斯医疗作为一家以医疗器械CDMO+CRO+CSO一站式服务为核心的创新服务公司分别与普瑞纯证医疗科技（广州）有限公司、上海皕晟管理咨询有限公司、广州众成大数据科技有限公司四家医疗器械服务企业共同就医疗器械CXO市场情况和产业现状发表了各自的观点和意见。
10-09
2023
2014上海全国医疗仪器设备|医疗器械博览会
10-09
2023
2014年全国医疗展
10-09
2023
2015第二十七届国际医疗仪器设备展览会
10-09
2023
2015年第二十八届印尼国际医疗医院制药及实验室设备展览会
10-09
2023
2015德国MEDICA展览会
10-09
2023
2016年迪拜医疗展
Transformation plan
a24
Solutions for traditional enterprises transforming into instrument manufacturers (Class II)
Solve the capital cost and time cost of various links such as enterprise production line preparation, quality system, product process, clinical trial, sample production, registration, etc. After one and a half years of certification, the capital cost was reduced by 86% and the time cost was reduced by 50%.
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a25
Solutions for traditional enterprises transforming into instrument manufacturers (Class III)
Resolve the capital and time costs of various aspects such as enterprise production line establishment, quality system, product technology, clinical trials, sample production, registration, etc. Obtained certification in 3 years, reducing capital costs by 89% and time costs by 40%.
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