Physician-Scientist Foundation
Tabinda trained as a physician before moving into clinical research, and she reviews protocols with both clinical and operational judgment.
Clinical research and regulatory affairs consulting
TeleT LLC is led by Tabinda Ali, MBBS, MS, CCRC. She has spent more than ten years in clinical research across academic and ambulatory settings, and she leads every engagement herself.
TeleT LLC is a clinical research and regulatory affairs consultancy founded by Tabinda Ali, MBBS, MS, CCRC. She holds a medical degree from Baqai Medical University and a Master of Clinical Research from The Ohio State University, where she graduated with a 4.0 GPA.
Her work covers clinical trial management, IRB compliance, quality assurance, data coordination, and regulatory strategy in academic and ambulatory settings. Through TeleT LLC, she offers that experience to sponsors, sites, and research organizations.
FDA submission strategy, IND and IDE applications, and regulatory document management for drugs, biologics, and devices.
Site activation, protocol development, feasibility assessment, and study management from start-up through closeout.
IRB applications, protocol amendments, SAE and DSMB reporting, and informed consent development.
Risk-based monitoring, GCP audits, SOP development, and corrective action planning.
EDC setup and oversight, source data management, CRF review, and data quality assurance.
Protocols, informed consent forms, clinical study reports, and regulatory briefing documents.
Tabinda trained as a physician before moving into clinical research, and she reviews protocols with both clinical and operational judgment.
She has worked in academic and ambulatory research settings for more than ten years and currently serves as Portfolio Manager in Michigan Medicine’s Clinical Trial Support Office.
You work with Tabinda from the first call to the final deliverable. Questions, drafts, and decisions go to her, not to an account team.