11/15/2014
LC-MS/MS Bioanalytical Method for Formoterol improved
As part of its increasing experience in the development and validation of bioanalytical methods for respiratory drugs Anapharm Europe has improved the limit of quantification for analysis of Formoterol achieving a LLOQ of 0.2 pg/mL in Human Plasma.
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Anapharm Bioanalytics Brazilian ANVISA Certificate Renewal
Anapharm Bioanalytics is proud to announce that it has recently renewed its ANVISA (Brazil) certificate.
The renewed certification is valid until 11th June 2020.
Anapharm Bioanalytics GLP Certificate Renewal
After the corresponding regulatory inspection Anapharm Bioanalytics has renewed once more its Certificate for Good Laboratory Practice Principles (GLP). The company is under GLP certification since its foundation. The present certificate is valid until June 2020.
READ MOREAnapharm Bioanalytics has participated in the III Workshop on Phase I Clinical Trials
The presentation of our Bioanalytical Coordinator, Araceli Castillo, was focused on two trending topics on Bioanalysis: the final guidance on Bioanalytical Method Validation published by the US FDA on May 21st, 2018 and the progress on the new guideline ICH M10 for the harmonization of bioanalytical method validation.
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