Quality Assurance

Quality Assurance

To demonstrate our technical commitment to excellence we abide by the most stringent medical guidelines

 

Medical Device Directives

Operating in accordance with The Medical Device Directive. Steroplast work to the guidelines of BS EN ISO 13485:2016 supported by: The Medical Device Directive (M.D.D.) 93/42/EEC: and our Wholesale Dealers of Licence.

Our "Quality Assurance System" is there for your peace of mind and is maintained under the supervision of our notified body: S.G.S. All our products are supported by our quality system which ensures compliance with the *Medicines & Healthcare products Regulatory Agency (M.H.R.A.)


TinyG

TiNYg Partnership

In alignment with our commitment to safety and ethical business practices, Steroplast Healthcare has partnered with TINYg, a global non-profit organisation devoted to the prevention of terrorism and enhancing security. This collaboration underscores our dedication to contributing positively to community safety and well-being.

By working with TINYg, we extend our commitment beyond healthcare, supporting initiatives that provide valuable information and resources to professionals in various sectors, including corporations, law enforcement, and academia. 


MHRA

How our CE mark benefits you:

All Steroplast medical devices carry the CE mark. This is our 100% guarantee that through our internal quality assurance department and the *M.H.R.A. all our products exceed all E.U. standards.


Greater Manchester Chamber of Commerce

Steroplast is a member of the Greater Manchester Chamber of Commerce

We are happy to be one of the 4500 members of the Greater Manchester Chamber of Commerce, which offers business support to companies in the Greater Manchester area.