Mesa Labs is pleased to announce the addition of a new suite of validation services and the launch of the new website validation.mesalabs.com.
Utilizing products such as Mesa’s Biological Indicators and real-time DataTrace data loggers, Mesa puts its extensive experience to work ensuring that your equipment, systems and processes are working as intended, properly and reliably.
Mesa’s new service offerings include:
- IQ/OQ/PQ Protocol Generation to meet the cGMP, ISO, FDA, and EC requirements of your operation.
- Protocol Execution to ensure that all execution is done correctly and adheres to cGMP practices, assuring your regulatory compliance.
- Final Report Generation to accurately document the results of the protocol execution.
- Deviation and CAPA investigation and resolution.
- Good Documentation Practices are observed during all phases of the Qualification or Validation.
Let Mesa’s Validation Services team take the worry out of meeting your regulatory requirements by managing the qualification, validation, commissioning and qualifying of your:
“Mesa’s Global Services team is perfectly suited to execute these various services,” says Dave DeWire, Sr. Director of Instrument Sales. “Our trained staff will work closely with the customer to develop targeted protocols that will incorporate our wealth of knowledge of regulatory requirements, blended with the critical nuances of our customer’s unique needs. Our team of experts will take the complexity out of the regulatory challenges our customers face and provide a turnkey and seamless solution to meeting all of their cGMP requirements.”
To learn more about Mesa’s range of validation services or to speak with an expert about your validation needs, visit validation.mesalabs.com.
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