WE HELP INNOVATE AND OPTIMIZE YOUR BUSINESS
Development and innovation can easily go hand-in-hand with compliance and GxP. Something we make sure of at DIS/CREADIS. We’re with you from start to finish in projects involving pharma/medico and medical devices, to make sure the right skills get you to your goal.
Process automation, digitization, and sustainability. There are many current trends in the life science industry, with enormous potential for ambitious pharmaceutical enterprises.
DIS/CREADIS can be your trusted advisor, because we understand your business, technology, and the law within the field. You can safely let us help you with a project, whether developing new medicines, medical devices, or optimizing your production plant and facilities.
DIS/CREADIS can help from start to finish with bespoke automated systems and facilities.
DIS/CREADIS can help optimize production or develop your products to be competitive, reliable, and compliant.
WE WEIGH THE RISKS WITH YOU
It takes experience and specialists to develop a business in a highly-regulated industry such as life science, whether optimizing production or achieving fast time-to-market. We can help you risk assess, create synergy, and reap the potential benefits of innovation and customized technology – within the framework of general and industry-specific regulations and standards such as GDPR, HAACP, the European Medical Devices Directive, and ISO 9001:2000.
We have mastered the documentation requirements and quality control, and every project we are involved in complies with regulatory requirements and fulfils GMP – and ultimately protects the end user.
Sustainability is an integral part of our business. DIS/CREADIS works according to the UN Sustainable Development Goals to enhance innovation and build sustainable forms of industry and production (SDG 9 and 12), something reflected in our deliveries to customers.