Gillson Sciences
About Gillson Sciences · ISO 17025 Accredited

Advancing Human Health
Through Science

Our mission is to empower clients to deliver safe, effective products that improve lives — with a commitment to scientific integrity, responsiveness, and partnership at every step.

Our Mission & Values
ISO 17025 Accredited cGMP Compliant FDA-Registered
Advancing human health across PHARMABIOTECHMEDICAL DEVICEHEALTHCARENUTRITION
Our Mission

Advancing Human Health Through Science

Our mission is to empower clients to deliver safe, effective products that improve lives. With a commitment to scientific integrity, responsiveness, and partnership, Gillson Sciences is your trusted ally in navigating complex regulatory landscapes and driving innovation in human health.

"A world where science empowers healthier lives."

Our Values

Innovation

Pushing boundaries with advanced technology and fresh thinking

Collaboration

Working as a true extension of your quality team

Courage to Act

Bold, informed decisions when your timelines demand it

Integrity

Every result accurate, defensible, and fully traceable

Putting Others First

Client success is the measure of our own — your compliance is our commitment

Our Approach

Scientific rigor, regulatory expertise, and genuine partnership.

Analytical & Microbiological Testing

Comprehensive testing for product safety and efficacy — from particulate matter and sterility to endotoxin and microbial limits.

Environmental Monitoring & Facility Validation

Cleanroom compliance programs designed to ISO 14644 and EU Annex 1 — viable air, surface, and personnel monitoring.

Consulting & Regulatory Advisory

Expert guidance on method development, validation, and regulatory strategy — from feasibility through submission-ready documentation.

How it works

From inquiry to compliance-ready report.

1

Scope your testing

Our scientific team reviews your requirements and recommends the right testing methods, standards, and timeline — same week.

2

Submit your samples

Complete our sample submission form, then ship samples per our instructions. Clear sample requirements, packaging guidance, and chain-of-custody provided.

3

Accredited testing

Your samples run in an ISO 17025 accredited lab under cGMP quality systems.

4

Actionable results

Compliance-ready reporting your quality team can file — with scientists on call to interpret.

Our Locations

FDA-registered laboratories across the U.S.

With locations spanning the country, Gillson Sciences delivers consistent, accredited testing close to where your products are manufactured and released.

Gillson Sciences laboratory locations across the United States
The Gillson difference

A testing partner, not just a test report.

Gillson Sciences supports the pharmaceutical, biopharmaceutical, medical device, healthcare, nutrition and cosmetic industries at every stage — detecting contamination risk while keeping you compliant and moving.

GxP-qualified experts, end to endFrom logistics through results delivery — one accountable team.
Scientifically rigorousGxP-qualified scientists delivering audit-ready, cGMP-compliant results across every method.
Audit-defensible documentationEvery result aligned to USP compendial standards and FDA GMP guidance — across all testing areas.
"Gillson Sciences has become an extension of our own quality team — accredited, responsive, and genuinely expert. They keep our products compliant and our timelines on track."
VP of Quality · Global Pharmaceutical Manufacturer
Questions

Frequently asked

How fast can testing start?
Quotes typically go out within one business day, and samples can be submitted as soon as scope is confirmed. Standard turnaround varies by method — your quote includes committed timelines, which we hit 99.8% of the time.
How does sample submission work?
We provide clear sample submission instructions and packaging guidance with chain-of-custody documentation. Complete our submission form, ship your samples, and results arrive without any site visits required. Onsite collection is also available for select services.
Which standards do you test against?
Our methods span USP, EP, JP, BP, ISO, ASTM, and EPA standards — covering pharmaceutical, biopharmaceutical, medical device, environmental, and nutritional testing requirements. Specific compendial references are cited in every test report, and additional methods are available per regional or product-specific regulations.
What accreditations do your labs hold?
We hold two ISO/IEC 17025 accreditations: an ANAB ISO 17025 Certificate of Accreditation from the ANSI National Accreditation Board, and a PJLA ISO/IEC 17025:2017 Certificate (Testing L23-642-1 / Calibration L23-641) from Perry Johnson Laboratory Accreditation. Our laboratories are also FDA-registered.
Can you handle ongoing programs, not just one-off tests?
Yes — we support the full molecule-to-market continuum. That includes early feasibility testing, method development and validation, clinical material release, commercial batch release, stability programs, environmental monitoring, facility qualification, and regulatory submission support. Most clients begin with a single method and expand as their program grows. From bench to bedside — one partner supporting your product from early development through commercialization.
Do you work with international clients?
Yes. We accept samples globally. Our reports are designed to meet international regulatory expectations, with methods aligned to USP, EP, JP, BP, ISO, and ASTM standards.
Let's talk science

Contact Us.

Tell us what you’re testing — a scientist responds within one business day.