ISO 9001 is the most internationally known quality management standard, which enables companies to serve their customers better and ensure that products and services always meet the requirements of both customers and authorities. ISO 9001 certification plays a significant role in implementing sustainable business because reducing errors and deviations saves costs. The certificate is reliable proof that the company operates in a customer-oriented and systematic manner in quality development.
The ISO 13485:2016 standard defines the requirements for a quality management system for use in organizations that need to demonstrate their ability to provide medical devices and related services that regularly meet the requirements of customers and authorities. The organization can be involved in one or more stages of the life cycle of a medical device, such as design and development, production, storage and distribution, installation, and maintenance, as well as the design, development, and production of services related to medical devices (e.g. technical support).
Finland's Strongest certificate tells customers, partners, creditors, and other stakeholders that cooperation with the company is on a sustainable basis. With the help of the certificate, the company can stand out from its competitors, gather positive attention, and strengthen its brand image. It is awarded only to the best of the best companies that have met the strict conditions and a high Rating Alfa credit rating.
The use of all management standards is expanding worldwide and in Finland. Quality management systematically aims for better operations, in which case customers are more satisfied, staff feels better, operations are more economical, profitable, efficient, and sustainable - and there are fewer risks. Quality management is a coordinated activity to direct and guide the organization in matters related to quality, i.e. in practice the management of the organization. A certified quality system helps the work community to make its operations more efficient and also identifies danger factors related to normal operations and exceptional situations.
The ISO 13485:2016 standard defines the requirements for a quality management system for use in organizations that need to demonstrate their ability to provide medical devices and related services that regularly meet the requirements of customers and authorities. The organization can be involved in one or more stages of the life cycle of a medical device, such as design and development, production, storage and distribution, installation, and maintenance, as well as the design, development, and production of services related to medical devices (e.g. technical support).
Finland's Strongest certificate tells customers, partners, creditors, and other stakeholders that cooperation with the company is on a sustainable basis. With the help of the certificate, the company can stand out from its competitors, gather positive attention, and strengthen its brand image. It is awarded only to the best of the best companies that have met the strict conditions and a high Rating Alfa credit rating.
The use of all management standards is expanding worldwide and in Finland. Quality management systematically aims for better operations, in which case customers are more satisfied, staff feels better, operations are more economical, profitable, efficient, and sustainable - and there are fewer risks. Quality management is a coordinated activity to direct and guide the organization in matters related to quality, i.e. in practice the management of the organization. A certified quality system helps the work community to make its operations more efficient and also identifies danger factors related to normal operations and exceptional situations.
Would outsourcing procurement and assembly be the
most productive solution for your company?
most productive solution for your company?
