Who is accountable here.
Every study is run by a credentialed regulatory team with hands-on manufacturing and investigator experience — and every inquiry reaches a person.
The Beacon regulatory team
Quality Review & Principal Investigator of Record
Beacon Life Sciences operates under a credentialed Principal Investigator of record with a Master’s in Biopharmaceutical Regulatory Affairs, cGMP cell-therapy manufacturing experience, and active responsibility on multiple ClinicalTrials.gov-registered observational studies. Every Quality Review is performed by our credentialed team — bringing the regulatory machinery of large-CRO operations to independent physicians, biotech sponsors, and patient-access programs.
Scientific and ethics oversight on registered observational studies is provided through our affiliation with Healing Hope International, a 501(c)(3) research organization.
Credentials & affiliations
- M.S., Regulatory Affairs — Northeastern University
- Graduate Certificate, Biopharmaceutical International Regulatory Affairs — Northeastern University
- B.S., Chemistry (biochemistry concentration) — University of Louisiana at Lafayette
- Two years of cGMP cell-therapy manufacturing and cleanroom operations
- Principal investigator of record on ClinicalTrials.gov-registered observational studies
- Good Clinical Practice (NIH) · HIPAA · CITI conflict-of-interest training
- Members: Alliance for Regenerative Medicine, ISCT, ISSCR, American Society of Regenerative Medicine
- Peer-reviewed publication — Computational Biology and Chemistry (2016)
- Expanded-access and compassionate-use program design across multiple indications
Want the person behind the review?
Every Quality Review is performed by the credentialed team under the PI of record — and inquiries reach a human.