Clinical research and regulatory affairs consulting

Trial. Evidence. Leadership. Execution. Trust.

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.

Education
MS, Clinical Research, The Ohio State UniversityMBBS, Baqai Medical University
Certification
CCRCCertified Clinical Research Coordinator
Experience
More than ten years in clinical researchAcademic and ambulatory settings

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.


  1. 01

    Regulatory Affairs Consulting

    FDA submission strategy, IND and IDE applications, and regulatory document management for drugs, biologics, and devices.

  2. 02

    Clinical Trial Operations

    Site activation, protocol development, feasibility assessment, and study management from start-up through closeout.

  3. 03

    IRB & Compliance

    IRB applications, protocol amendments, SAE and DSMB reporting, and informed consent development.

  4. 04

    Quality & Auditing

    Risk-based monitoring, GCP audits, SOP development, and corrective action planning.

  5. 05

    Data Management

    EDC setup and oversight, source data management, CRF review, and data quality assurance.

  6. 06

    Medical Writing

    Protocols, informed consent forms, clinical study reports, and regulatory briefing documents.

Physician-Scientist Foundation

Tabinda trained as a physician before moving into clinical research, and she reviews protocols with both clinical and operational judgment.

Institutional Experience

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.

Founder-Led, Every Time

You work with Tabinda from the first call to the final deliverable. Questions, drafts, and decisions go to her, not to an account team.

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