CS Analytical Laboratory

Activities: Containment Manufacturing

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  1. What is ISO 8 cleanroom classification? Each cleanroom class is denoted by a maximum concentration of particles per cubic meter or cubic foot of air. ISO 8 is the second lowest cleanroom classification
  2. Impact of the new Annex 1 on sterile filling in pharma EU GMP Annex 1 is a whole new era for the sterile filling industry. From barrier technology to “first air”, pharmaceutical manufacturers have a lot to decide. Johannes...
  3. Danish pharmacies invest in hi-tech environmental monitoring system The construction of a new building prompted one of Denmark’s largest pharmacy businesses to invest in Vaisala’s viewLinc Continuous Monitoring System (CMS) to protect the...
  4. Industry 4.0: What is the advantage of real-time digital signage? Olivia Fernandez from Digital Therapeutics (DTx) disusses how digital signage can serve in cleanrooms as a versatile and powerful tool that allows those in charge to ensure...
  5. Scientific justification for monitoring indirect product contact surfaces Findings from a survey on several pharma companies unveil the best practices for monitoring indirect product contact surfaces. Walid El Azab and Lillia Belkhamassi explain

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CS Analytical Laboratory names new Director of Quality

Sandra Cincotta has joined the cGMP, FDA-registered and inspected contract laboratory exclusively designed and dedicated to container testing
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