Loopa Logic introduces its clinical quality and operations advisors
Meet three advisors bringing GCP quality assurance, manufacturing inspection experience, and sponsor clinical operations perspectives to Loopa.
Loopa’s advisory group brings together practitioners with experience in clinical quality, inspection readiness, and sponsor operations. Their contributions help inform how Loopa organizes study evidence, supports reviewer decisions, and fits into clinical monitoring workflows.
Paula Casasco
Clinical quality and review workflowsPaula advises Loopa on clinical quality and the procedures used to review and triage potential findings. She authored Loopa’s triage workflow and contributes to procedures for reviewer overrides and escalation, bringing a quality assurance perspective to how decisions are documented.
Kimberly Kiner
Inspection readinessKimberly has advised Loopa since late 2025. She began her career as an FDA investigator in manufacturing compliance before moving into clinical research, GCP auditing, and training. Her work with Loopa focuses on inspection readiness and the documentation supporting clinical review and oversight.
Domingo Rodriguez, M.D.
Sponsor clinical operationsDomingo brings more than 30 years of experience across biotechnology, pharmaceutical, and medical device companies. His background includes global clinical development and leadership of clinical-stage programs in the United States and abroad. He advises Loopa on sponsor clinical operations and how its approach fits within sponsor and CRO workflows.
These perspectives inform the development of Loopa’s review workflows and documentation. Clinical teams remain responsible for assessing the evidence and making decisions within their assigned roles.