Minimum Order Quantity | 1 Certificate |
Service Location | PAN India |
Service type | Online |
Type of Industry | For Manufacturing |
Services offered | Consultancy |
EIR | Broadband telecommunications company |
Document verification | Online |
Service Location | PAN INDIA |
Document verification Mode | Online |
Certification Provided with in | 30 Days |
Type of Industry | For Manufacturing |
Services offered | Consultancy |
Service Location | PAN INDIA |
Document verification Mode | Online |
Services offered | Consultancy. |
Type of Industry | for Manufacturing |
Certification Provided | with in 30 Days |
ISI Certification For Potable Water Bottles (Copper, Stainless Steel, Aluminum) is something we offer to meet the different needs of our clients. These ISI Certification services are done with parts that are guaranteed to be of good quality and at prices set by the industry. On top of that, these ISI certification services are available at prices that are easy on the wallet.
Service Location | Pan India |
Certification Provided with in | 30 Days |
Services offered | Consultancy |
Document verification Mode | Online |
Certifications Provided | ISI |
Minimum Order Quantity | 1 Certificate |
Service Location | Pan India |
Mode of Report | Soft Copy |
Service Mode | Online |
Payment Mode | Online / Offline |
Service Type | ISO Registration Certification |
Certifications Provided | ISO 45001:2018 |
Target Location | Pan India |
Mode of Report | Soft Copy |
Type of Certification | New Certification |
Document verification Mode | Online |
Application | Occupational Health And Safety Management System |
Certifications Provided | CDSCO |
Target Location | Pan India |
Document verification Mode | Online |
Type of Certification | New Certification |
Type of Industry | Medical |
Mode of Report | Soft Copy |
The Indian medical regulatory system has become more stringent in recent years. In past, medical devices did not need to be approved at all, but that is not the case today. In India, there are about 30 device “families” that outline which specific medical devices need to be registered under Medical Devices Rules, 2017. Medical Device Rules, 2017 came into force in January 2018 and devices are regulated by the Central Drugs Standard Control Organization (CDSCO). The Central Drugs Standard Control Organization (CDSCO) is a regulatory body that lays down stringent standards that any drug, medical devices, diagnostic kits, cosmetics, biologicals and vaccines being introduced into the country must meet before being sold in the market.