Since our inception, we have been strengthening our industry relationships and building our knowledge of an ever-changing biopharmaceutical industry. CRI Lifetree has a clear understanding of the issues and challenges that our clients face when developing a new chemical entity or reformulating an existing product. With that in mind, we have structured the company to be the right size organization to be responsive and to provide our clients with the best in the industry—unparalleled service, a team that is deeply rooted in science, an academically minded team without the red tape of academia, easy-to-access our Clinical and Thought Leaders and a foundation built firmly on quality.
CRI Lifetree holds itself to the highest standard of ethics and integrity with the goal of exceeding our client’s expectations. We are committed to the highest level of quality in the performance of clinical research and the protection of human subjects. CRI Lifetree is committed to providing high quality clinical data, which are accurately supported by source documentation, based on applicable GCP regulations, related guidance documents and CRI Lifetree Standard Operating Procedures (SOPs) and Work Instructions (WIs). CRI Lifetree has established A Quality Management Program and will obligate to maintain this program in order to meet these commitments.
Every member of the CRI Lifetree Team is focused on exceeding our client’s expectations. We pride ourselves on being accountable and are attentive to meeting the accelerated timelines our clients expect.
We recognize that our clients expect quality data and our "repeat clients” are evidence of our commitment to excellence in every aspect of our work.