Med Device Online18h
Key QMS Considerations For Your Medical Device Startup
A quality management system (QMS) can often become bloated and unwieldy. This expert helps you understand key QMS basics and ...
Med Device Online6d
A Look At AI-Driven Medtech For Rare Disease Diagnosis
Recent advances in AI, including machine learning, natural language processing, and deep learning models, are transforming ...
Med Device Online13d
Most Frequently Asked Questions On The Revised EU GMP Annex 1: Volume 1
Annex 1 guidelines emphasize quality risk management, enhanced environmental monitoring, and data integrity, aiming to ...
Med Device Online6d
Meeting Annex 1 Regulations: A Proactive Approach To Regulatory Compliance
It was imperative for a large European CMO that produces multiple biologic drugs to select the right product quality and ...
Med Device Online5d
Electrical & Electronic Engineering
EDG engineers employ a wide variety of electronics technologies to create innovative solutions for your electronics design needs. EDG engineers employ a wide variety of electronics technologies to ...
Med Device Online7d
eTMF Clinical Trial Software For Life Sciences
Managing an electronic trial master file (eTMF) is a complex and labor-intensive effort. Centralize and streamline your clinical activities with MasterControl eTMF software systems. Administering a ...
Med Device Online14d
Achieving EU GMP Annex 1 Compliance Through An End-To-End Approach To Contamination Control
Gain insight into three areas that have been key in ensuring a robust contamination control strategy to help ensure ...
Med Device Online22d
Mastering EU MDR & IVDR: Certification Compliance For Medical Device Importers And Distributors
The European Union’s Medical Device Regulation (MDR 2017/745) and In Vitro Diagnostic Regulation (IVDR 2017/746) impose stringent requirements on all economic operators involved in the supply chain of ...