Beckman Coulter Life Sciences, a global leader in laboratory automation and innovation, continues its relentless commitment to providing laboratories of all sizes with individualized and tailored support to meet the evolving list of regional and global compliance requirements.
Cleanroom laboratories manufacturing sterile medicinal products in the European Union must make critical changes by August 25, 2023 to ensure Annex 1 Regulation compliance.
Anurag Tandon, Global Vice President, Quality Control and BioManufacturing, Beckman Coulter Life Sciences “Solutions from Beckman Coulter Life Sciences for analyzing total organic carbon, environmental monitoring and particle counting are used every day around the world to help ensure quality and safety in diverse applications,” Tandon continued.
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