Bringing Life-Enhancing Medical Devices Safely and Efficiently to Patients: A Guide
Authors: SelectScience | Last updated: June 26, 2023
Overview
Remaining competitive in the medical device market requires that manufacturers deliver innovative, quality, safe and effective devices for patients while complying with strict standards and regulations. In addition, manufacturing requires constant insight into renewable resources, sustainable materials, more energy efficient devices and methods to reduce waste.
This expert guide provides an overview of medical device quality control and manufacturing solutions for the entire development and production process to help meet biocompatibility, cleanliness, safety, and packaging standards.
- Document type: Guide
- Page count: 61
- Read time: 1 hour 25 minutes
Key Takeaways
- Compliant lab weighing and pipetting
- The importance of ultrapure water
- Reducing the risk of endotoxin contamination
- Viable air monitoring in sterile production environments
- Live-cell imaging for cytotoxicity evaluation
- More efficient lateral flow assay development
- Streamlined measurement of product attributes during biotherapeutic development
This Resource is Designed for:
- Medical Devices Manufacturers
- Lateral Flow Assay Manufacturers
Applications Supported:
Compliant lab weighing and pipetting
Importance of ultrapure water
Endotoxin contamination
Air Monitoring in sterile production environments
Live-cell imaging
Assay development: Surfactants and Membraes
Biotherapeutic development