
Bespak has contributed to the design, development and industrialisation of some of the world's leading medical devices. Bespak provides the capability and expertise to minimise time to market, allowing your products to be developed, tested and manufactured faster and with less risk. Through an in-depth understanding of 'design for manufacture' and a robust six sigma based improvement approach, Bespak offers an unrivalled ability to manage programmes from conception to maturity.
Core competencies include:
We have over time, invested substantially in the provision of robust regulatory and quality systems to ensure reliability in the development, manufacture and supply of our devices. These systems include a mature ISO9000 accreditation and an FDA 21CFR820 compliant quality system, which are frequently audited by our pharmaceutical partners.
We also offer a fully validated SAP system to control the supply chain, manufacturing and supply and all our sites operate to ISO13485, the MHRA standard for medical device manufacture.
Articles