ISO 8655 and FDA Audits
Regular FDA audits are required for all drug development labs, helping to ensure data integrity and proof of efficacy. However, supporting your science with the assurance of an ISO 8655 compliant pipette calibration service provider, ensures that the pipette measurements are accurate and reliable. As FDA audits validate proper drug development and quality controls, ISO 17025 accreditation audits provide the same integrity for pipette calibration providers. However, when an auditor evaluates compliance of a pipette service provider to ISO 8655 standards and controls, they are raising the bar and promoting standards-based calibration. For pipette service providers, ISO 8655 compliance improves service integrity, so drug development labs provide quality products, supported by trustworthy, reliable service providers.
To see how we can help you with your pipette calibration services, contact us at 1-800-242-6022 or email us at firstname.lastname@example.org.