Case Study: Elemental Analysis to Identify Contaminant in Brine SolutionsQuality Program
Reliability at Our Core.
The Impact Analytical quality program has been designed to comply with the ISO 9001:2008 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 numerous 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 staff personally ensures data reliability. If you have questions about our quality program, please e-mail one of the members of our quality team:
- Quality Manager – Sarah Diener
- Business Manager – Mike Murphy
- Business Marketing Manager – Eric Hill
- Lead ISO Internal Auditor – Celia Mendoza
- Quality Assurance Auditor – John MacLauchlan
A downloadable version of our ISO certificate can be found here: ISO Certification PDF
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