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Home » Articles

Articles

Cleanroom design & Classification | RS NESS

Cleanroom Design

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Cleanroom Construction Project

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Preparing your QMS for the EU MDR

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DHR is an essential requirement for Medical Device Company - RS NESS

How to establish DHR

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Guide: Roadmap of Medical Device - From Idea to the Market | RS NESS

Medical Device Roadmap from Idea to Market

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Packaging Validation in the Medical Device and Pharmaceutical Industries - R.S NESS

Your Packaging Validation Guideline

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The Nanosono journey- from idea to ISO13485 Certification

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Validation of Medical Device manufacturing line for getting the European CE mark certification.

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Supplier evaluation and approval in 5 steps | RS NESS

Supplier evaluation and approval in 5 steps.

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Preparing your QMS for the MDR: QA Best Practices | R.S NESS Solutions

Preparing your Quality Management System for the MDR: QA Best Practices

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Medical Cannabis company has only 2 months to be prepared for a scheduled EU-GMP audit | RS NESS

If you have 2 months to establish an EU-GMP compliant production line for Medical Cannabis, what should you do?

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Process validation difference between Pharma vs. Medical Device industries

Process Validation: Pharma vs. Medical Device

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Medical Device Single Audit Program (MDSAP) in 60 Sec | RS NESS

MDSAP In 60 Sec

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