Deviation Management Process
RS NESS is a highly experienced service provider in the Medical Device and Pharmaceutical industries.
We can assist you with CAPA and Deviation Management in helping you to create appropriate policies and process, as well as to optimize deviation handling.
Purchased Part Approval Process (PPAP)- the next step in supplier quality
RS NESS is a highly experienced service provider in the Medical industry.
We can assist you with a PPAP process implementation to help you create an appropriate and suitable process for your needs and improve your supplier quality.
Our expertise is in the field of Regulatory Affairs, Clinical Affairs, QA, Validation, and Engineering processes.
IVD Classification Under IVDR
RS NESS is a highly experienced service provider in the Medical industry.
RS-Ness can assist you with an IVDR gap assessment to help you create an appropriate project plan, and support the transition throughout the Regulatory, Clinical, QA, Validation, and Engineering processes.
We differentiate ourselves by being quality-oriented and by our technical expertise that comes with a hands-on experience and approach, ensuring that our clients receive the most effective and professional service.
Our clients range from small Start-Ups to international companies.
Butterfly effect due to a small part exchange in a Medical device company
RS NESS is a service provider and consulting company in the Life science industry for those who are unfamiliar with us.
RS NESS provides a variety of services such as project management, quality assurance, regulatory affairs, clinical affairs, validation and engineering services.
As an employee at RS NESS, in addition to our academic knowledge and practical training, we have been gifted by the ability to learn and adapt quickly, to combine our expertise with flexibility in order to provide the most professional service to our customers.
Cleanroom Design
RS-NESS works with various companies to construct production facilities and provide a comprehensive solution for these complex projects. We accompany the customer from the initial stages – planning in principle and obtaining approval of the facility and perform validations for equipment / systems /processes while accompanying and supervising the entire project on behalf of the customer.
If you have any questions, or if you need professional support, please contact us.
