Validation batches of Strangvac completed
Intervacc has, together with 3P Biopharmaceuticals and LIOF-Pharma (previously Praxis Pharmaceuticals), completed the manufacturing process for Strangvac. The validation production batches required for the forthcoming registration application to the European Medicines Agency, EMA, are thus finalized.
Submission of a registration application requires manufacturing of two batches in a scale that will be used for commercial production. The drug substance (antigens) for these batches have been produced during the summer and have been included as active components in the vaccine doses that
