Articles

Ensuring Business Continuity in Life Sciences

BD case study

Poka Yoke and Six Sigma

Computer System Validation

Risk Management in Medical Device

What Are Clinical Trials?

What are Clinical Trials?

DEVIATION MANAGEMENT PROCESS

Deviation Management Process

Purchased Part Approval Process (PPAP)

Purchased Part Approval Process (PPAP)- the next step in supplier quality

IVDR MEDICAL DEVICE CLASSIFICATION

IVD Classification Under IVDR

Butterfly effect due to a small part exchange in a Medical device company

Butterfly effect due to a small part exchange in a Medical device company

Cleanroom design & Classification | RS NESS

Cleanroom Design

Clean room establishment, Construction Project

Clean Room Construction Project

Preparing Your QMS For The EU MDR

Preparing your QMS for the EU MDR

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

How to establish DHR

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

Medical Device Roadmap from Idea to Market

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

Your Packaging Validation Guideline

The Nanosono Journey- From Idea To ISO13485 Certification

The Nanosono journey- from idea to ISO13485 Certification

Validation Of Medical Device Manufacturing Line For Getting The European CE Mark Certification.

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

Supplier evaluation and approval in 5 steps | RS NESS

Supplier evaluation and approval in 5 steps.

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

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

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?

Process validation difference between Pharma vs. Medical Device industries

Process Validation: Pharma vs. Medical Device

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

MDSAP In 60 Sec