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BioTech
High-sensitivity analysis for the pharmaceutical ensures that medications and active pharmaceutical ingredients (APIs) meet the highest standards of purity, safety, and regulatory compliance.
Our planned accreditation to ISO standards and operation within an ISO Class 6 cleanroom environment delivers precise, reliable testing that supports regulatory submissions, GMP manufacturing, and patient safety.
Our comprehensive analysis enhances quality control, mitigate contamination risks, and meet stringent global standards such as ICH Q3D.
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Environmental
Our lab provides rapid detection of contaminants in soil, water, air, and waste samples, supporting compliance with environmental standards such as UK Drinking Water Regulations, Waste Framework Directive, and REACH.
By partnering with Elemental Resolve, environmental professionals gain trusted, defensible data to guide remediation, sustainability, and regulatory strategies — helping to protect both people and the planet
CMOs and CROs
We support Contract Manufacturing Organizations (CMOs) and Contract Research Organizations (CROs) in meeting the highest standards of quality, compliance, and regulatory readiness.
Our services are designed to integrate seamlessly into manufacturing and research pipelines, ensuring that elemental impurity data is accurate, validated, and regulatory-compliant, including ISO 17025 standards with GMP-aligned practices.
Whether assisting with product development, clinical trial materials, or commercial manufacturing, our rapid and reliable trace metal testing helps CMOs and CROs manage risk, accelerate timelines, and maintain full regulatory confidence.