Supplier evaluation and approval in 5 steps.
RS-NESS supports Life Science companies in rapid scale-up and meeting GMP compliance requirements; proving the experience you need when you need it.
If you are planning a Supplier Evaluation and Approval process, contact us to discuss how we can support your goals.
Preparing your Quality Management System for the MDR: QA Best Practices
RS-Ness supports Life Science companies in QA, Regulatory Affairs, Clinical affairs, Validation and Project Management.
We will assist you with an MDR gap assessment to help you create an appropriate project plan, and support the transition throughout the Regulatory, Clinical, QA, Validation, and Engineering processes.
Our clients range from small Start-Ups to international companies.
If you have any questions, or if you need professional support, please contact us.
Moti Loitner
Engineering Director
If you have 2 months to establish an EU-GMP compliant production line for Medical Cannabis, what should you do?
RS NESS supports Life Science companies in rapid scale-up and meeting GMP compliance requirements; proving the experience you need, when you need it.
If you are planning your production validation, contact us to discuss how we can support your goals
