Category: Facility Monitoring

NewsMicrobial Contamination Monitoring and cleanroom data management Cleanroom Classification v. Cleanroom monitoring

Electronic Data in Pharmaceutical Manufacturing: Benefits of Paperless Reporting (Series Part 2 of 6)

In this six-part blog series, we examine common issues with data transfer, integrity, analysis, reporting and storage that we encounter as cleanroom owners and users every day. Weā€™ll explore how automation and electronic solutions, within the parameters of Regulatory Authorities and cGMP, can help improve efficiency and product quality.

NewsMicrobial Contamination Monitoring and cleanroom data management Cleanroom Classification v. Cleanroom monitoring

Upgrade from Pharmaceutical Net to FacilityProĀ® for effective cleanroom data management

Upgrading is a streamlined process made easy by the FacilityProĀ® systemā€™s user requirement specifications (URSs) of data integrity, automation, simplicity, integration, service and support.

NewsUSP 1116 Quality Risk Management

Quality Risk Management Applied to an Isolator Filling Line

Following the webinar, “Developing an Isolator Filling Line Using a Quality Risk Management Approach” the expert presenters answered questions around monitoring critical points in a cleanroom. Learn more…

Newscounting efficiency particle monitoring requirements

Particle Monitoring Requirements in Pharma Cleanrooms

Pharmaceutical manufacturers must demonstrate compliance with the regulations at every stage before a drug can be released to market. To satisfy these requirements, the products are manufactured in a controlled environment, known as a cleanroom. A cleanroom is the fundamental starting point for contamination control.

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