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Capability
01 Analytical Method Development (1)
Country
01 U.S.A (1)
- Service Details
ACTA performs cGMP method validation in accordance with USP and ICH requirements. Parameters normally validated are accuracy, precision, specificity, limit of detection, limit of quantitation, linearity, range and robustness. ACTA’s staff is highly experienced with method development for
- Directory Listing
Pharma Service: Analytical
Sub Category: Method Development and Validation