MDSS 欧盟授权代表 MDSS 企业咨询   英语    德语    简体中文
最新动态
  • Looking for a suitable GMDN-Code?
    MDSS can assist you to determine an appropriate code for your products!
    more


  • MDSS, may support you with the process of applying for a Certificate of Marketability...more


  • Update to IVD Directive...more

  • Update to MEDDEV Guidelines...more

  • Update to Portuguese Registration...more

  • Update to Vigilance Guideline...more

  • Update Harmonized Standards

    EN 980 is back...more



    
展会信息
Keep up to date!

News and Views March 2017

New Medical Device Regulation (MDR) in Europe
Read more...

In-House Workshops
The "NEW CE" mark
Book now!
 to make sure you’re ready to survive and thrive



重要事件
Meet us!

8. Medical Device Networking Meeting
Hanover, April 27, 2017




联系我们
MDSS GmbH
Schiffgraben 41
30175 Hannover
Germany

Phone
(+49)-511-6262 8630
FAX
(+49) -511-6262 8633

Click here to
contact us




供货商审查 (Supplier Audits)


供货商审查 (Supplier Audits)


您对您的供货商有任何疑问吗?他们提供的产品的质量和您所收到的样品的质量一致吗?

MDSS可以帮助您解开疑问。我们可以按照标准 EN ISO 13485 以及相关指令(90/385/EEC,93/42/EEC,98/79/EC)中的条款对您的供货商进行审查。我们确信,以我们在世界各国多年的审查经验,您将从我们这里得到准确而又满意的结果。您只需要联系我们,我们将非常乐意为您服务。


Contact us 请点击此处联系我们

返回主