LUNARIA spol. s r.o. (Ltd) is a private pharmaceutical Contract Research Organization (CRO) specializing in the analytical R&D and ICH stability studies of pharmaceutical products. We can support you with the number of analytical techniques you need to develop new solid and liquid dosage form formulations. Main activities: ICH Stability Studies with GMP manufacturing licence and FDA approval Photostability following ICH Q1A + ICH Q1B, automated Binder chamber Storage of Samples for Accelerated and Long – term Stability Studies, also 30 C/75 % RH Analytical Method Development, Validation and Testing, Pharmaceutical Pharmacopoeia Analytics in Accord with GMP, GMP manufacturing licence for human and veterinary drugs and Phase studies EU Analysis of Pharmaceutical Products, EU Test, EU Testing, EU Reanalysis and Batch Release with HPLC, UPLC, µHPLC, high-resolution LC/MS (HR-NMR), CAD, mass balance, forced degradation studies, dissolution studies, freeze/thaw studies, and other Analytical Expertise.