Certification is recognized as a procedure by which our center gives a written guarantee in writing that a service, a product, a process comply with fully specified requirements.【详细】

According to the 874 Decision (November 20, 2012), the Commission of the Customs Union introduces a New Technical Regulation on the safety of grain, which will acquire legal force from July 1. This standard will be determined by standards, detailed assessment requirements, and the procedure for issuing a certificate for grain products.【详细】

In connection with the systematic transition of the Russian certification system to a new harmonization scheme with international standards, ETS technical regulations are becoming most relevant. A new system of “technical regulations certification” is being systematically introduced and a limitation on the validity periods of previously issued declarations and certificates in accordance with GOST R. is being introduced.【详细】

俄罗斯GOST技术法规证书-俄罗斯TR认证-Technical Regulations GOST Certificate The Russian certification system today carries out a systematic transition from traditional standardization - assessing the quality of manufactured products according to GOST R. This is evidenced by numerous technical regulations (hereinafter referred to as TR) that replace the GOST standards and their number is constantly growing every year. So what is TR?【详细】

EAC豁免函-VNIIS豁免函-俄罗斯海关豁免函-VNIIS Rejection letter，Rejection letter In the certification system, a refusal letter means an official conclusion of an information and legal nature. A document intended for participants in economic market activities in the territory of the Russian Federation and abroad.【详细】

TR CU Certification, EAC Mark, TR Certification【详细】

俄罗斯防爆认证（CU-TR 012/2011，标志是EAC-EX）是强制性文件之一，它赋予了与某些类型的工业设备和设备一起工作的权利，其名称通常是添加防爆字母Ex。在石油、化工、能源等领域，对于在易燃易爆环境中作业的产品设备，以及产品本身具有易燃易爆性质的，这类产品在进入俄罗斯市场销售时会需要做俄罗斯防爆EAC认证。【详细】

俄罗斯医疗器械分类和欧盟医疗器械分类几乎完全一致，一般可以参照欧盟的分类进行。Medical Device (MDD)（医疗器械指令） 93/42/EEC 1.1.1995～15.6.1998/4/3 In Vitro Diagnostic Device (IVDD) （体外诊断医疗器械指令） 98/79/EC 7.6.2000～12.7.2003 考虑医疗器械之设计及制造对人体可能带来的危险程度，可将医疗器械分为以下4类:【详细】