追加説明:
PMRS has validated hundreds of analytical methods since 1994 across dosage forms such as tablets, capsules, creams, and extrusions, developing methods to client specifications or its own SOPs and validating them under FDA and ICH guidelines. It also specializes in residual cleaning verification to confirm manufacturing equipment cleanliness, alongside ICP-MS testing, microbiological services, and X-ray particle diffraction testing.
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