Quality control (QC) testing for Active Pharmaceutical Ingredients, excipients, and finished products. Our QC analytical laboratories ensure compliance to current specifications, from raw materials to finished product. Galenica has quality control systems that require strict adherence to GMP regulations.
All pharmaceutical development activities require thorough stability considerations. Our range of storage capabilities are fully compliant with ICH guidelines.
As part of the Galenica pharmaceutical services, we provide regulatory consulting. We assist you through the regulatory hurdles associated with drug development facilitating approval of submissions.
Every initial contact starts with a discussion between Galenica and your development team. After an evaluation phase the outcome of these discussions results in a project proposal and a quotation along with a suggested contract framework.