About Element Ann Arbor
Element Ann Arbor is an FDA-registered and DEA-licensed (schedules 1-5) laboratory, bringing chemists and scientists together to tackle scientific product development challenges in the biopharmaceutical industry and across other industries and applications. Our laboratories are GLP/GMP-compliant, ISO 17025 accredited and QP authorized for clinical trial material in the EU.
Throughout each step of product development, our scientists and experts work within a rigorous quality system to ensure products comply with regulatory requirements and consumer expectations.
Located in the Detroit Metro area, Element Ann Arbor offers complete, comprehensive scientific solutions that support the entire product development life cycle, with a focus on growing strategic partnerships.
Interested in learning more about Element's comprehensive pharmaceutical testing capabilities? Download a copy of the pharma testing capabilities brochure.
Standards we test to and things we test
- Biopharmaceutical products
- Clinical trial materials
- Pharmaceutical products
- Scientific product development materials
- FDA registration (laboratory compliance)
- DEA licensing (Schedules 1-5)
- GLP (Good Laboratory Practice) compliance
- GMP (Good Manufacturing Practice) compliance
- ISO 17025 accreditation
- QP (Qualified Person) authorization for clinical trial material in the EU
Global expertise
Working with Element, you have access to our global network of materials testing and product qualification test experts. Meet our Engaged Experts.
Speak to our team of experts
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