型号:生物力学科研技术服务
联系人:李先生
联系电话:18618101725
品牌:BMM ,flexercell
世联博研(北京)科技有限公司(Bio Excellence International Tech Co.,Ltd)简称世联博研,专注生物力学和3D生物打印国际前沿科研设备的销售、租赁及科研技术服务,产品线涵盖细胞分子生物力学、组织修复生物力学、血管力学生物学、骨与关节生物力学、口腔力学生物学、眼耳鼻咽喉生物力学、康复工程生物力学、生物材料力学与仿生学、人体运动生物力学等生物力学研究以及3D生物打印前沿领域科研利器。
世联博研联合欧美生物力学专家,为生物力学测试提供了方位的服务(生物材料、组织和生物医学产品)。除了使用我们的技术执行高度控制的测试外,我们的专家团队还遵循有效的标准操作程序,制定可靠的测试协议,并根据良好的实验室实践和GLP提供准确的数据分析报告。作为我们服务的延伸,提供设计和制造符合客户te定研究要求的配件。我们与客户和三方CRO合作,在短时间内提供个性化的测试解决方案。
Bioexcellence offers a full-service approach to mechanical testing of biomaterials, tissues and biomedical products. In addition to performing highly controlled tests using our state-of-the-art technology, our expert team adheres to effective standard operating procedures, develops reliable testing protocols and delivers accurate data analysis reports in compliance with the GLPs. We collaborate with our clients and third-party CRO’s to supply personalized testing solutions within a short time frame to suit our customers objectives
我们为每个客户和每项研究调整和执行不同的测试、不同的样本和不同的分析。有时会与客户一起设计新的SOP和协议,设计和开发新的附件来执行不同于我们通常做的测试类型,执行不同于我们习惯的分析。
We offer a wide variety of mechanical tests for biomaterials, biological tissues and biomedical products. You might think your test idea is complex and hard to perform - we encourage you to share your idea with our study director. Every study is unique and we customize our services to match your specific needs - we adapt and perform different tests, different samples and different analysis for every client and every study. We, sometimes design new SOPs and protocols along with our clients, design and develop new accessories to perform different test types than what we usually do, perform different analysis than what we're used to - we're flexible! Please visit our Case Studies section to see a few examples of studies conducted by our team.
为确保产品和服务质量实施严格的质量控制提供证据。符合ISO 13485:2016和EN ISO 13485:2016(医疗器械)、FDA 21
QUALITY MANAGEMENT SYSTEM
We recognize our responsibility as a provider of medical devices, mechanical testers and laboratory testing services to the most stringent quality standards. To this end, we have developed and documented a strong Quality Management System which provides evidence of strict quality controls implemented to ensure product and service quality. It complies with ISO 13485:2016 and EN ISO 13485:2016 (Medical Devices), with the FDA 21 CFR Part 820, with the European MDD 93/42/EEC and with the Canadian Medical Device Regulations 1998-783.
在非临床研究中,良好实验室规范(GLP)是指研究实验室管理控制的质量体系,以确保结果的一致性、一致性、可
·伤口愈合评估
·药丸粘附试验
·啮齿类动物股骨扭转试验
·培养细胞的双轴刺激
·软骨修复评估
·海藻酸钠珠的机械评估
·水凝胶特性
·小鼠股骨三点弯曲、不规则表面三维压痕测试、结缔组织压缩期间电位分布等