Bioequivalence Studies

Pharmasolutions can conduct the following studies: Full and partial replicate studies,  
Cross over and parallel studies, Fasting and fed studies. All studies are conducted as per the ethical committee approved protocol, SOPs, current GCP, GLP standards and applicable regulatory requirements. Bioanalytical methods are developed and validated in accordance with the GLP rules and guidelines of FDA and EMA. Each step of the study is audited and verified by Quality assurance (QA) unit.