CBR International Corp.® is an integrated development company supporting all aspects of the product development life cycle including clinical, scientific, quality and regulatory. With clients around the globe, CBR provides services to support filings and approvals in the United States, Europe, Canada, South America, Asia and Australia. CBR has expertise across a wide range of indications for drugs, novel antibodies, recombinant protein therapeutics, small molecules, vaccines, cell therapy, device and combination products throughout all phases of program development (Phase I – IV) and commercialization. CBR International’s expertise and services are globally relevant. Our current clients are located worldwide, and are typically looking to gain approvals in the U.S., Europe, and other regions.
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TruSubmit LLC is a premier provider of end-to-end eSubmissions solutions for the Biotechnology and Pharmaceutical Industries Worldwide. With over 15 years of experience working with U.S. and international clients to prepare and submit drug applications to the FDA and other regulatory agencies worldwide, we are your partner in going electronic. We specialize in the preparation, compilation, and publication of submissions in the eCTD format. We provide end-to-end services from the creation of submission-ready documents through publication, and can tailor our services to meet your needs.