Significant safety concerns can exist for residue materials used in or for pharmaceutical compounds or medical devices. USP 467 is recognized by the FDA and provides a testing method and defined safety levels. Piper Medical's experience and state of the art, GLP compliant, laboratory can provide the unbiased, quality data and analysis necessary to meet your product objectives. If your testing requirements are part of a larger FDA regulatory strategy, our extensive experience with the FDA can make your job easy. Furthermore, because we work with the FDA on a regular basis, our detailed understanding of the FDAs reporting requirements can greatly enhance and speed your regulatory application or validation process.

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Analytical Chemistry Services

Assay Development Impurity Detection HPLC Testing GC/MS Testing VOC Testing