⚙️ Manufacturing Process Overview

🏭 Facility Requirements

Clean Room Specifications

• Classification: ISO 7/Class 10,000
• Environmental Controls: Temperature, humidity, pressure
• Monitoring: Continuous air quality tracking
• Documentation: Complete production records

🔬 Production Process

Synthesis Protocol

1. Raw Material Preparation: Phosphate precursors
2. Initial Reaction: Controlled synthesis conditions
3. Modification Steps: Surface and functional additions
4. Purification: High-purity isolation
5. Quality Verification: Testing at each stage

✅ Quality Control

Testing Parameters

• Chemical Purity: >99.5% target compound
• Structural Integrity: Spectroscopic verification
• Functional Activity: Binding assays
• Stability Profile: Temperature and pH testing

Release Criteria

• Composition: Meets specifications
• Activity: Functional performance verified
• Safety: Toxicity assessments passed
• Stability: Shelf-life requirements met