MEENA CHETTIAR - Eventura

Step-by-Step approach for Setting up FDA Audit Ready Quality Management System (QMS) – Case Studies based training

Duration: 90 Minutes

A to Z of Supplier Management in the Medical Device Industry

Duration: 90 Minutes

MDSAP Audits – All You Need to Know

Duration: 75 Minutes

Dealing with Out of Specification (OOS) Test Results

Duration: 75 Minutes

Good Preparation Practices for FDA Audits and Responding to FDA 483s

Duration: 60 Minutes

Handling OOS Test Results As Per Latest FDA Guidance -2022

Duration: 90 Minutes

Quality by Design (QbD) in Pharmaceutical and Medical Device Manufacturing

Duration: 75 Minutes

ISO 13485:2016 Requirements and Compliance to Latest Updates

Duration: 75 Minutes

FDA Quality System Inspection Technique (QSIT) Audits – Good Preparation Practices

Duration: 75 Minutes

Preparing yourself for Compliance to ISO 13485:2016

Duration: 60 Minutes

Test Methods and Standards for Design Verification & Validation

Duration: 75 Minutes

ISO 13485:2016 – Proposed Changes to the International Medical Device Standard

Duration: 60 Minutes

Design Verification, Validation and Testing for Medical Devices

Duration: 60 Minutes