We are helped by the synergies resulting from our close collaboration with the VIVATIS Pharma API department. And since it is often not just quality and cost-effectiveness that matter, but also speed, we also place great emphasis on efficiency.
International and European standards and regulations form the basis for all VIVATIS Pharma Intermediates activities. VIVATIS Pharma holds numerous REACH registrations, and we can help our clients to evaluate and register their own new substances.
VIVATIS Pharma fully complies with all international and European standards and regulations. Audits can be conducted on all suppliers. Many clients require complete solutions, especially for intermediates sources in Asia. Depending on the project, these solutions can include conducting our own audits, supervising client audits with qualified staff with relevant language skills, monitoring batches, carrying out feasibility studies and or further processing of intermediates. In delivering these solutions, our Intermediates team is able to draw on a wealth of experience and an extensive network.