The core activity of Cilatus BioPharma Consulting AG is to advise and support biopharmaceutical companies in the following areas: CMC development and manufacturing (Chemistry, Manufacturing and Controls), regulatory affairs, quality assurance, certification of Qualified Persons (QP), conceptual engineering, GMP manufacturing (Good Manufacturing Practice), quality management systems, auditing, and CDMO search and management (Contract Development and Manufacturing Organization). The company supports its clients in developing and implementing strategies, conducting audits, and ensuring compliance with regulatory requirements. It also provides consulting services in the areas of quality assurance, GMP manufacturing, and quality management systems.