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
Monthly Archive: July 2020
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
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