MSME Certificate

MSME certificate is a valid proof of registration. This is issued post a successful registration for one business

MSMEs not only play crucial role in providing large employment opportunities at comparatively lower capital cost than large industries but also help in industrialization of rural & backward areas, thereby, reducing regional imbalances, assuring more equitable distribution of national income and wealth.


Certification Levels and Cost of Certification Zero Defect and Zero Effect (ZED) is a simple, transparent and affordable certification with 3 levels i.e., Bronze, Silver and Gold, and is based on well defined parameters of Quality, Safety, Production, Cleanliness, Energy, Environment and more.

The ZED certification will be issued by Quality Council of India after reviewing the site-assessment report.

The goods and services tax (GST) is an indirect federal sales tax that is applied to the cost of certain goods and services. The business adds the GST to the price of the product, and a customer who buys the product pays the sales price inclusive of the GST.

With GST, the taxation system of our country has become simpler. It is a single tax, ensuring easier calculation. With this tax, the buyer gets a clear idea of the amount paid as tax when purchasing certain products. This is crucial when considering GST and its impact on the GDP.

UDYAM Certificate

An Udyam Registration Certificate is an e-certificate issued on the completion of your MSME registration process.

An Udyam Registration, also known as an MSME Registration, comprises of a government sign-off provided along with a Recognition Certificate and a Unique Number. This is instrumental if you wish to certify that your small or medium business or enterprises is legal and operational.

ISO Certificate

ISO 13485 is designed to be used by organizations involved in the design, production, installation and servicing of medical devices and related services. It can also be used by internal and external parties, such as certification bodies, to help them with their auditing processes

ISO 13485 was written to support medical device manufacturers in designing a QMS that establishes and maintains the effectiveness of their processes. It ensures the consistent design, development, production, installation and delivery through to disposal of medical devices that are safe for their intended purpose.

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