We are dedicated to consistently meeting the highest quality standards while maintaining strict compliance to cGMP and ISO 9001:2015 standards. Our continuous improvement culture has driven our quality management system to ensure the delivery of safe and efficacious pharmaceutical products. We are proud to offer custom APIs and excipients as well as DEA controlled substances. Our quality and regulatory affairs team is responsible for creating & maintaining our Drug Master Files (DMFs), Annual Reports to FDA, Amendments and international registrations. We strive to stay ahead of changes in legislation, regulations, guidance, and industry standards. We have an excellent track record with all regulatory bodies (FDA, DEA & ISO) and will always welcome customer audits.