The Impact Analytical quality program has been designed to comply with the ISO 9001:2000
quality system standards. 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 many successful customer quality audits.
Impact Analytical will provide products and services
that meet or exceed the expectations of our customers
through our commitment to continuous improvement
in everything we do.
– Impact Analytical Quality Statement
Our dedicated quality staff is able to partner with you to ensure data reliability. If you have
questions about our quality program, please e-mail one of the members of our quality team:
Do you have a particular analytical, testing, or consulting service need?