Fortifying Contamination Control: Innovative Strategies for Pharmaceutical and Medical Device Industries
In partnership with: American Pharmaceutical Review | Last updated: March 2024
Overview
When it comes to contamination control strategy, microbiology, cleanroom monitoring, and barrier technology, staying informed and proactive is essential. The importance of these areas is underscored by the FDA recalls and market trends. According to FDA data, a significant number of recalls are due to issues related to contamination and inadequate control measures. In addition, market trends show a growing emphasis on stringent cleanroom standards and advanced barrier technologies to ensure product quality and consumer safety.
This eBook will delve into these critical topics, providing insights, best practices, and the latest developments to help professionals navigate the complex landscape of contamination control and microbiology in the pharmaceutical industry.
- Document type: eBook
- Page count: 45
- Read time: 59 minutes
Key Takeaways
- Latest trends and FDA insights on contamination control and its impact on recalls
- Best practices for cleanroom monitoring and barrier technology implementation
- How to effectively manage microbiological quality control in non-sterile manufacturing
- How to apply GMP Annex 1, EN 17141 and ISO 14698 standards
This Resource is Designed for:
- People Working in QC Labs
- Medical Devices Manufacturers
- QC Microbiologist
- QC/QA Manager
- Microbiology Manager
Applications Supported:
- Pharmaceutical Quality Control (QC)
- Medical Devices
- Microbiological QC
- GMP Annex 1
- Quality Risk Management and Contamination Control Strategy
- Non-Sterile Manufacturing
- Cleanroom Monitoring
- Contamination Control Strategy
- Barrier Technology
- Air Monitoring
- EN 17141
- ISO 14698
- MD8 Airscan®
- Bioburden Control
- Microbial Enumeration
- Purified Water & Water for Injection
- Mycoplasma Detection
- Real-Time PCR Assay