-
Intertek certification
As one of the world's largest consumer product testing, inspection and certification companies, Intertek is renowned worldwide for its recognized expertise, quality and integrity. Relying on a global service network covering more than 100 countries, Intertek has become a trusted partner of global customers by providing the highest standards of fairness, accuracy, high-quality services and innovative solutions.
-
ROHS certification
RoHS certification is a mandatory standard established by EU legislation. Its full name is "Restriction of Hazardous Substances". This standard has been officially implemented since July 1, 2006. It is mainly used to regulate the material and process standards of electronic and electrical products to make them more beneficial to human health and environmental protection.
-
TUV Medcial CE certificate
CE ‘European Conformity’. CE marking states that a product meets the requirements of all applicable EU directives. TÜV SÜD provides companies around the world with CE mark testing and can also create technical documentation that shows products are compliant.
CE marking assures your product can enter the European Union and allows free movement throughout the nearly 30 countries that make up the European Economic Area, giving you direct access to over 500 million consumers. If a product that should display a CE mark is found not to have one, the manufacturer or distributor could be fined and face expensive product recall – so compliance is essential.
-
CNAS certification
Laboratory CNAS accreditation is an evaluation of the management and technical capabilities of laboratories by CNAS in accordance with prescribed standards. Having the CNAS mark means that the institution has been accredited by the China National Accreditation Service for Conformity Assessment and has the technical capabilities to carry out testing and school-level services in accordance with relevant international accreditation standards.
-
MHRA certification
The full name of MHRA is Medicines and Healthcare products Regulatory Agency. MHRA is the government department in charge of medicines and medical devices in the UK. Both pre-market and post-market supervision of medical devices will be supervised by MHRA.
-
FDA certification
FDA (Food and Drug Administration) certification is a food or drug certificate issued by the U.S. government's Food and Drug Administration. Due to its scientific and rigorous nature, this certification has become a world-recognized standard. Drugs that have obtained FDA certification can be sold not only in the United States, but also in most countries and regions in the world.
-
Intertek certification
As one of the world's largest consumer product testing, inspection and certification companies, Intertek is renowned worldwide for its recognized expertise, quality and integrity. Relying on a global service network covering more than 100 countries, Intertek has become a trusted partner of global customers by providing the highest standards of fairness, accuracy, high-quality services and innovative solutions.
-
ROHS certification
RoHS certification is a mandatory standard established by EU legislation. Its full name is "Restriction of Hazardous Substances". This standard has been officially implemented since July 1, 2006. It is mainly used to regulate the material and process standards of electronic and electrical products to make them more beneficial to human health and environmental protection.
-
TUV Medcial CE certificate
CE ‘European Conformity’. CE marking states that a product meets the requirements of all applicable EU directives. TÜV SÜD provides companies around the world with CE mark testing and can also create technical documentation that shows products are compliant.
CE marking assures your product can enter the European Union and allows free movement throughout the nearly 30 countries that make up the European Economic Area, giving you direct access to over 500 million consumers. If a product that should display a CE mark is found not to have one, the manufacturer or distributor could be fined and face expensive product recall – so compliance is essential.
-
CNAS certification
Laboratory CNAS accreditation is an evaluation of the management and technical capabilities of laboratories by CNAS in accordance with prescribed standards. Having the CNAS mark means that the institution has been accredited by the China National Accreditation Service for Conformity Assessment and has the technical capabilities to carry out testing and school-level services in accordance with relevant international accreditation standards.
-
MHRA certification
The full name of MHRA is Medicines and Healthcare products Regulatory Agency. MHRA is the government department in charge of medicines and medical devices in the UK. Both pre-market and post-market supervision of medical devices will be supervised by MHRA.
-
FDA certification
FDA (Food and Drug Administration) certification is a food or drug certificate issued by the U.S. government's Food and Drug Administration. Due to its scientific and rigorous nature, this certification has become a world-recognized standard. Drugs that have obtained FDA certification can be sold not only in the United States, but also in most countries and regions in the world.
-
Intertek certification
As one of the world's largest consumer product testing, inspection and certification companies, Intertek is renowned worldwide for its recognized expertise, quality and integrity. Relying on a global service network covering more than 100 countries, Intertek has become a trusted partner of global customers by providing the highest standards of fairness, accuracy, high-quality services and innovative solutions.
-
ROHS certification
RoHS certification is a mandatory standard established by EU legislation. Its full name is "Restriction of Hazardous Substances". This standard has been officially implemented since July 1, 2006. It is mainly used to regulate the material and process standards of electronic and electrical products to make them more beneficial to human health and environmental protection.
-
TUV Medcial CE certificate
CE ‘European Conformity’. CE marking states that a product meets the requirements of all applicable EU directives. TÜV SÜD provides companies around the world with CE mark testing and can also create technical documentation that shows products are compliant.
CE marking assures your product can enter the European Union and allows free movement throughout the nearly 30 countries that make up the European Economic Area, giving you direct access to over 500 million consumers. If a product that should display a CE mark is found not to have one, the manufacturer or distributor could be fined and face expensive product recall – so compliance is essential.
-
CNAS certification
Laboratory CNAS accreditation is an evaluation of the management and technical capabilities of laboratories by CNAS in accordance with prescribed standards. Having the CNAS mark means that the institution has been accredited by the China National Accreditation Service for Conformity Assessment and has the technical capabilities to carry out testing and school-level services in accordance with relevant international accreditation standards.