Reliability at Our Core.
The Impact Analytical quality program is certified to the ISO 9001:2008 quality system standard. Upon client request, analytical services and method validations can be conducted in compliance with Good Laboratory Practice (GLP) regulations required by the EPA or FDA or current Good Manufacturing Practice (cGMP) regulations required by the FDA. Impact Analytical is a registered facility with the FDA (Registration Number 3004518270).
Impact Analytical is also licensed with the Drug Enforcement Administration (DEA) to maintain and test controlled substances under DEA Schedules II, III, IIIN, IV and V.
Clients are always welcome to schedule an on-site visit to conduct an audit of our laboratories and operations. We have hosted numerous successful customer quality audits.
Impact Analytical will meet the customer's expectations at every point of contact. We will accomplish this through a commitment to continual improvement of our communication, work processes, and delivery of service to the customer.
– Impact Analytical Quality Statement
Our dedicated staff personally ensures data reliability. If you have questions about our quality program, please e-mail one of the members of our quality team:
A downloadable version of our ISO certificate can be found here: ISO Certification PDF