We value your company, your ideas,
and your business.
BrevisRefero is a collection of highly experienced biopharma consultants who share a common goal - to improve and support the management of biologics programs from post-discovery through to development, GMP manufacturing, and into clinical trials.
Our team comes from all walks of industry including CDMO's, sponsor companies, research and development organizations, and more. This diverse range of experience allows BrevisRefero's technical team to fully and holistically support our clients Chemistry, Manufacturing, & Controls (CMC) programs to ensure products make it into clinical trials.
With over 100 years of collective experience pushing biologic drug development programs forward, your company and products are in secure hands with our team.
Enhancing the value of our client companies through long-term relationships
Since our establishment in 2010, we have helped an extensive list of clients prepare for (and deliver) GMP drug products in support of Phase I-III human clinical trials. What's more, the vast majority of our clients have been with us for the long-term, meaning that the value we create as CMC experts continues to make an impact on our client's organizations over the long-term. This is primarily due to our deep and extensive experience in effectively managing third-party relationships at CDMOs, CMOs, and CROs, which directly translates to bringing our clients a competitive advantage through effective and sustainable technical program management.