TR

Pharmaceutical analysis

Conducting research in the field of finished dosage forms, substances and excipients. Development of methods for the analysis of new drugs. Pharmaceutical analysis laboratory services

Comparative test of dissolution kinetics as an addition to the bioequivalence study
Result: quantitative
Research method: UV spectrophotometry,
HPLC-UV/ELSD


Comparative test of dissolution kinetics for additional dosages
Result: quantitative
Research method: UV spectrophotometry,
HPLC-UV/ELSD and UPLC-UV/ELSD


Development and validation of methods for the analysis of substances and drugs
Result: qualitative and quantitative
Research method: UV spectrophotometry,
HPLC-UV/ELSD and UPLC-UV/ELSD, dissolution test, TLC, pH-metry, K.Fischer method and other methods.


Analysis of substances and medicinal products in accordance with ND / FSP
Result, qualitative and quantitative
Research method: UV spectrophotometry,
HPLC-UV/ELSD and UPLC-UV/ELSD, dissolution test, TLC, pH-metry, K.Fischer method and other methods.


Writing and reviewing regulatory documentation

Compilation and verification of regulatory documentation based on the research