Determine the biosimilarity profiles of your molecule with our comprehensive biosimilarity packages, including our characterization capabilities, regulatory services and our readily available biosimilars.
Biosimilar products are clinically equivalent, non-identical copies of an originator biologic product and hold immense promise in improving:
From early to late-stage development, we are experts at biosimilars manufacturing and have a track record for bringing them to the market at an accelerated rate. With expertise and experience in developing and launching biosimilar products worldwide— spanning the EU, USA, MENA and LATAM — we are ready to expedite your journey to market.
We ensure your biosimilar product meets the highest quality and safety standards. Aligned with regulatory agencies such as the EMA and USFDA, our state-of-the-art analytical techniques and expert scientists provide accurate and reliable characterization data, giving the confidence and assurance you need in your biosimilar product.
Our comprehensive regulatory services support you in navigating the complex regulatory landscape. We work closely with you and domestic and international regulatory bodies to provide guidance on regulatory compliance and submissions, including the preparation of dossiers supporting common technical document (CTD) filings from preclinical studies to marketing authorization application (MAA). We are committed to helping you meet the highest standards of quality and safety while ensuring cost-effectiveness and timely delivery.
Our readily available biosimilars include:
With a proven track record and robust biosimilars pipeline, we are committed to supporting your biosimilar development and manufacturing program to help expand healthcare accessibility worldwide.