- Coordinate transferring validated testing methods seamlessly from the Analytical Research & Development (R&D;/ADL) lab over to the routine QC lab.
- Execute shortened verification protocols for official pharmacopeial methods (USP, BP, EP, JP) to ensure they work under your specific laboratory conditions
- Ensuring the method detects the active drug without interference from impurities or excipients.
- Confirming how close results are to the true value and their repeatability.
- Testing if minor deliberate changes (e.g., fluid pH, temperature) impact results.