Contaminants or particles in the air greatly impact the process of both testing and manufacturing samples and products. While maintaining laboratory quality standards has always been critical, the increased focus on strictly controlled environments will continue to expand with stem cell research and regenerative medicine demands.
One of the most impactful precautions laboratories and clinical manufacturers can take in avoiding contamination is establishing and maintaining a cleanroom that meets Good Manufacturing Practice (GMP) guidelines. Understanding which factors can threaten cell cultures, how cleanroom classes are defined, and the importance of cleanroom certified equipment is critical for success.
Download this application note to learn about cleanroom certified equipment.