Next-Gen Sterile Sampling System: Pinnacle Compliance - USP Standards 87, 88, 85, 661.1, 788, 71, and ISO 11737-1 for Unparalleled Pharma & Biopharma
Sterile sampling system is a critical component in the pharma and biopharma industries to ensure the safety, quality and integrity of products during their manufacturing processes. It involves aseptic collection of samples from various stages of production, such as raw materials, intermediates, final products, and environmental monitoring with Pharmacopoeia compliance and Biocompatibility which is highly recommended for critical applications with a wide range of sampling unit values 50 - 1000.
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Asset 5: Introducing: Ami Polymer's Sterile Sampling Systems
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Topics
- Advanced therapies manufacturing
- AI, analytics and decision support
- Ami Polymer
- Biologics formulation and stability
- Bioprocessing and biomanufacturing
- CDMO/CMO operations
- Chromatography and separations
- Clinical Trials
- Continuous manufacturing and PAT
- Controlled release and advanced delivery
- Drug Development
- Drug-device combination products
- Endotoxin
- Environmental Monitoring
- ESG and regulatory drivers
- Excipients and raw materials
- Formulation and drug delivery
- GMP and quality management systems (QMS)
- Parenterals and sterile injectables
- Raw materials and supply chain (bioprocess)
- Regulation and compliance
- Spectroscopy and imaging
- Sterility and rapid methods
- Therapeutics
- Upstream processing
