MM2PA4VP1
Milliflex Oasis® Customer Validation Protocol in A4 format
Sign Into View Organizational & Contract Pricing
All Photos(2)
About This Item
UNSPSC Code:
41116500
NACRES:
NB.79
Recommended Products
application(s)
bioburden testing
pharmaceutical
water monitoring
compatibility
for use with MILLIFLEX®
General description
Microbiological monitoring and testing in the pharmaceutical industry are highly regulated and a very complex field. In our long history of serving the pharmaceutical industry by pioneering and refining ground-breaking solutions, we have gained the regulatory and technical expertise to make compliance as simple as possible, and help save your valuable resources, by providing comprehensive range of professional and best-in-class services. Our Customer Validation Protocol makes validation faster, easier and ensures that your Milliflex Oasis® pump, accessories and related consumables do comply with the validated specifications. Our bioburden validation protocols follow international guidelines such as EP/USP and GMP.
With our best-in-class services you can:
With our best-in-class services you can:
- Optimize your QC lab workflow and ensure regulatory compliance
- Rely on comprehensive and ready-to-use validation packages
- Ensure the performance of your Milliflex Oasis® pump while reducing the risk of breakdown
Application
Our validation protocols are based on our internal product qualification test methods. These extensive protocols will enable the QC/QA lab to quickly initiate the validation master plan and perform IQ, OQ and PQ (suitability of the test methodology) with ease.
Features and Benefits
Count on our comprehensive and ready-to-use validation protocols consisting of the following sections:
1. Validation Master Plan: Define structure, responsibilities for qualification
2. Installation Qualification (IQ)
4. Performance Qualification (PQ) Test Method suitability verification (microbiology validation procedures)
5. Final Report Summarizes all testing performed for final approval of validation
1. Validation Master Plan: Define structure, responsibilities for qualification
2. Installation Qualification (IQ)
- Verification and identification of with your Milliflex Oasis® pump, accessories and related consumables
- Verification of product′s utilities and operating environment requirements
- Equipment and personnel preparation
4. Performance Qualification (PQ) Test Method suitability verification (microbiology validation procedures)
5. Final Report Summarizes all testing performed for final approval of validation
Legal Information
MILLIFLEX is a registered trademark of Merck KGaA, Darmstadt, Germany
MILLIFLEX OASIS is a registered trademark of Merck KGaA, Darmstadt, Germany
Certificates of Analysis (COA)
Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Related Content
Microbial membrane filtration with the Milliflex Oasis® vacuum pump and filtration funnels for bioburden and water testing.
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service