CCIT Challenge sets
Designed to Meet Global Pharma Integrity Standards
Container Closure Integrity Testing (CCIT) ensures that sterile pharmaceutical containers remain sealed against microbial ingress, moisture, and gas exchange throughout shelf life. Even micro-leaks as small as 5 microns can compromise drug sterility.
Mahant Pharma Advances offers precision-calibrated CCIT test kits containing vials, ampoules, and syringes with engineered micro-holes and cracks for validation purposes. These kits simulate realistic packaging defects to test the sensitivity of your leak detection systems.
- Vacuum decay
- Helium leak detection
- High-voltage leak detection (HVLD)
- Laser-based headspace analysis
- Pressure/dye ingress
Our kits are customizable by container type, defect size, and material, with full traceability and certificates of defect authenticity. Each unit is suitable for LoD determination, system calibration, and regulatory validation (IQ, OQ, PQ).
Mahant also offers training, SOP development, and requalification support to ensure your teams are audit-ready and competent. We help benchmark your CCIT equipment’s accuracy and repeatability to USP <1207> and EU GMP Annex 1 expectations.
By partnering with Mahant Pharma Advances, manufacturers gain independent, third-party assurance that their packaging integrity testing is robust, validated, and regulatory compliant.
Challenge the Impossible
Test your skills with real-world scenarios designed to sharpen your critical thinking, creativity, and innovation. Are you ready to solve what others can’t?