TAMI (IMI) Central R&D; Inst.
Font Size:
Site Colors:
Accesskey
S - Skip navigation
1 - Home page
4 - Search
Accessibility Statement
Method Development and Validation

Method Development and Validation

Our staff at the QC Pharma lab have vast experince in developing analytical methods and method verification/validation including stability indication methods (SIM). this is done under GLP / cGMP guidlines with support from our QA unit. After validation we use the methods for rutine analyses for our clients, or we transfer them to the clients (tech transfer) with all the required support from our experts.