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CAPA for Medical Devices: Common Mistakes and How to Avoid Them
The Corrective and Preventive Action (CAPA) process is crucial for maintaining quality a
Nov 28, 2024
# CE marking
# MDSAP
# TCP III
# ISO 13485
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PSUR for Medical Devices under EU MDR: Preparation and Submission
The preparation and submission of Periodic Safety Update Reports (PSURs) are crucial res
Nov 22, 2024
# CE marking
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Key Objectives and Content of a Periodic Safety Update Report (PSUR)
The Periodic Safety Update Report (PSUR) under the Medical Devices Regulation 2017/745 (
Nov 15, 2024
# CE marking
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The new TISAX® labels: what to consider
As a standardized assessment and exchange mechanism for information security in the automotive indus
Nov 08, 2024
# TISAX (Information Security in the Automotive Industry)
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How to Improve Efficiency & Ensure Safety in Pharmaceutical Packaging Manufacturing
How Can You Improve Efficiency and Maximize Safety in Pharmaceutical Packaging Manufacturing? In th
Oct 31, 2024
# Primary packaging materials for medicinal products
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Understanding Periodic Safety Update Reports (PSUR) for Medical Devices
Compliance with the Medical Device Regulation 2017/745 (MDR) requires manufacturers to prepare a Per
Oct 24, 2024
# CE marking
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