A skilled team with extensive analytical expertise allows LEF to provide services for a wide range of pharmaceutical compounds and dosage forms.
Analytical Method Development and Validation
Assay Methods for Raw Material and Finished Product
Dissolution
Related Substances Methods for Raw Material and Finished Product
Stability-indicating Assay / Forced Degradation Studies
Preservatives&Antioxidants Assays
Colouring Agents Identification
Microbiological Methods Development and Validation
Validation of the recovery of micro-organisms in the presence of product to microbiological examination and preservatives efficacy tests
Sterility Test Validation
Cleaning Validation
Equipment and Facilities Cleaning Validation Program
Development and Validation of Analytical Methods for Cleaning Validation
Setting Acceptable Residue Limits
Release Testing and Percutaneous Absorption Testing
In vitro Release Tests and Percutaneous Absorption, using Franz Type Cells with Human Tissues.
Equipment
LEF’s analytical development laboratories are equipped with a wide range of fully qualified equipment such as HPLC with UV/Vis, PDA/DAD, RI and Fluorescence detection, LC-MS/MS and GC-MS/FID.