Pharmaceutical Formulations as well as packaging materials are tested
for compliance with the reported specifications at the modern and
well-equipped QC laboratories.
The expert staff at QC with best training and motivation using
the most up-to-date logical methods e.g. LC-, UV-, IR-, NIR-spectroscopy,
GC, dissolution, particle size tests etc. for pharmaceutical materials.
Testing of storage stability is performed according to the ICH
Guideline recommendations.
Modern climatic rooms with technical monitoring are also available
here at Oboi's facility. Our microbiology department is responsible
for the microbiological monitoring program according to the transparency
that demands for all pharmaceutical materials. Additional analytical
investigations as well as development and optimization of analytical
methods are performed by a special team of the QC department. |
