12/01/2012
Anapharm Europe acquires a new high sensitivity equipment
The new equipment allows the determination of extremely low concentration of compounds such as Fluticasone, Salmeterol, Budesonide, Formoterol, Tiotropium, Ethinyl Estradiol, Paricalcitol, etc. In biological fluids.
As part of its efforts to continue to support drug development of women health and inhaler products, Anapharm Europe has purchased a new equipment targeted for method validation with limits of quantification in the low pg/mL level. The AB SCIEX QTRAP 5500 increases our capabilities for the determination extremely low concentrations of compounds such as Fluticasone, Salmeterol, Budesonide, Formoterol, Tiotropium, Ethinyl Estradiol, Paricalcitol, etc. in biological fluids.
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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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