STERILE DISINFECTANTS
We understand the importance of Pharmaceutical & Healthcare providers to be in line with the current GMP standards & regulations when introducing disinfectants to be used in a critical area/Cleanroom. Annex 1 introduces tighter regulations and fills in gaps with updated regulations to both EU GMP and US FDA when dealing with contamination and residue control solutions.
QuantumTec’s USP Grade disinfectants assists Pharmaceutical manufacturers and Healthcare industry when making tough and important choices.
Daily disinfection/cleaning use
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- IPA 70/30 with WFI
- Denatured Ethanol 70/30 with WFI
Sporicide and rotational use
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- Hydrogen Peroxide 6% with WFI
- Sodium Hypocholorite 0.52% with WFI
Wide area & broad spectrum disinfectant
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- Quaternary Ammonium concentrate.
Residue Removal Detergent
All products comes with either Sterile or Non-Sterile options.
Key feature of QuamtumTec product line up includes:
- Certified ISO manufacturing facility
- Production in line with Good Manufacturing Practices (GMPs)
- Locally manufactured in Malaysia.
- Validated Sterility Assurance Level (SAL = 10-6) for sterile products
- Technical data and Test reports are readily available.
- Ready to use bottles keeps contamination control in check.
- Bag in bottle design. Sterile content remains sterile.
- Certificate of Analysis and Irradiation are included with each batch/lot produced.
- Document availability eases audit proses