NRT Smoking Cessation
Zeptide Pharma operates a state-of-the-art GMP Clean Room Environment
All purification and post-purification processing—including lyophilization (freeze-drying) and primary packaging—take place within our ISO Class 5 (Class 100) clean room suites.
- Environmental Monitoring: Continuous tracking of particulates, pressure, and humidity to mitigate the risk of cross-contamination.
- Sterile API Processing: Specialized protocols for endotoxin control and bioburden reduction, essential for injectable peptide therapeutics.
- Qualified Equipment: Our systems undergo rigorous IQ/OQ/PQ (Installation, Operational, and Performance Qualification) to meet global health authority requirements.
