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Laser Diffraction Particle Size Analysis | Materialsmetric.com

Materials Metric provides laser diffraction particle size analysis services for powders, suspensions, emulsions, and nanoparticle systems. Laser diffraction generates accurate, reproducible particle size distributions across a broad dynamic range, from submicron particles to millimeter-scale granules. Their scientists operate both wet and dry dispersion laser diffraction systems and apply appropriate sample preparation protocols to ensure measurement accuracy. Particle size data is critical for formulation development, process control, regulatory submissions, and performance characterization of drug delivery systems, biomaterials, and industrial powders. Results are reported with full distribution statistics (D10, D50, D9 and expert interpretation to support client objectives.

https://materialsmetric.com/pa....rticle-size-morpholo

Biofilm Testing | Materialsmetric.com

Materials Metric delivers specialized biofilm testing services for medical devices, biomaterials, and antimicrobial surface coatings. Their biofilm analysis capabilities include biofilm formation and resistance studies, antimicrobial efficacy testing, structural characterization using advanced microscopy, and aerobic and anaerobic culture testing. These services help device manufacturers assess infection risk, validate antimicrobial claims, and optimize surface treatments. Materials Metric employs standardized and custom biofilm models using clinically relevant organisms, providing quantitative data on biofilm inhibition, eradication, and structural disruption. Results are presented in comprehensive technical reports supporting product development decisions and regulatory submissions.

https://materialsmetric.com/bi....ofilm-analysis-servi

Supplier change risk assessment | Materials Metric

A supplier change risk assessment is the structured process of evaluating how a change in raw material source, formulation, or manufacturing site may affect product safety, compliance, and performance — and it is one of the most critical steps any regulated manufacturer can take before approving a new or alternate supplier.

https://materialsmetric.com/20....26/07/supplier-chang

Material change biocompatibility | Materials Metric

Material change biocompatibility assessment is required whenever a medical device undergoes a change in raw materials, suppliers, or manufacturing processes — because even minor modifications can introduce new chemical risks to patients. Regulatory agencies, including the FDA and ISO standards bodies, mandate a documented biological evaluation any time such changes occur, regardless of how small the alteration appears.

https://materialsmetric.com/20....26/07/material-chang

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