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Most clinical programs don’t fail in the lab.
They stall in protocols, operations, and regulatory friction.

We troubleshoot the entire development chain. Find the root cause, fix the right problem.

About ABBE Consulting

Abbe Consulting exists for the moments when trials slow down and the root cause isn't obvious.

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Most programs don't fail in science. They stall in the system: protocol design decisions, site execution, data strategy, and regulatory alignment.

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We troubleshoot across the entire drug and device journey. With 20+ years spanning clinical sites, CROs, academia, regulatory agencies, biotech, and industry, founder Dr. Stephanie Tan brings a full-pipeline perspective that connects the dots others miss.

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What sets us apart:

  • Systems thinking: We find failure modes across protocol, ops, data, and regulatory, not just one function.

  • Practical execution: Clear decision memos, prioritized actions, and hands-on support when needed.

  • Outcomes: Fewer amendments, cleaner data, faster activations, stronger reviewer narratives, and submission readiness.

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Engagement is flexible: rapid diagnostic, embedded troubleshooting, advisory, or team training, tailored to your urgency and resources.

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If timelines are slipping, screen failures are rising, amendments keep looping, or reviewer feedback circles back to design and feasibility, we help you fix the right problem and move forward with confidence.

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Dr Stephanie Tan MD MMed MBA

Principal Consultant

I'm the call when timelines slip and no one agrees why.

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Over 20 years across clinical sites, CROs, academia, regulatory agencies, biotech, and industry, I've seen the entire drug and device development journey and where it breaks.

That 360-degree view lets me see what others miss: how a protocol decision becomes site confusion six months later, how eligibility ambiguity drives screen failures, how a protocol–SAP disconnect surfaces at database lock.

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My work is straightforward: diagnose the failure modes, fix the root cause, and move programs forward. Fewer amendments, cleaner data, faster decisions, stronger submissions.

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I work flexibly: rapid diagnostics, embedded troubleshooting, retainer advisory, or team training, depending on what your program needs and when.

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Credentials

  • MBBS, MMed (University of Melbourne) | MBA (Melbourne Business School)

  • Executive education: Stanford Graduate School of Business, Harvard Medical School

  • Former Regional Medical Advisor, IQVIA

  • Former academic appointments: Lee Kong Chian School of Medicine, NUS, National University Health System

  • Author: IIT Made Easy

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Operating Principles

  • Systems thinking over silos 

  • Evidence first, plain language always

  • Partner with your team and CROs

  • Decide fast; document why

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What Clients Say

Medical Desk Setup

"Stephanie represents a rare composite of clinical studies, commercial experience, and academic excellence. She is thoroughly versed in the logistics, administration, and execution of all aspects of clinical research. At a personal level, she is a straight talker and excellent communicator, very approachable and easy to work with. She is able to meet targets and goals in an expedient manner. I have no hesitation in recommending her for any research-related matters."

— Professor Seng Gee Lim, MBBS (Hons), FRACP, FRCP, FAMS, MD
Director of Hepatology, National University Health System, Singapore

"Dr. Stephanie Tan and her team provided invaluable guidance throughout the entire process, from developing the study protocol to analyzing the results. They were highly knowledgeable and experienced in all aspects of clinical trial design, implementation, and analysis, and always available to answer questions and offer expertise. Their insights and recommendations helped in many aspects of my clinical studies. I highly recommend ABBE Consulting to any researchers in need of expert guidance and support. They were an essential partner in the success of our trial."

— Dr. Poh Seng Tan, MBBS (Hons), MRCP (UK), MMed (Int Med), FRCP (Edin), FAMS
Senior Consultant, Gastroenterology & Hepatology, Mount Elizabeth Hospital, Singapore

"Stephanie has deep expertise in clinical trials, especially Investigator-Initiated Trials. She generously shares that knowledge for the benefit of clients. Her industry insight helped us enter a new market segment and streamline go-to-market planning and strategy. She is responsible, client-focused, and detail-oriented, which makes her stand out. We collaborated for about two years, and it was a pleasure to learn from and work with her. She would be a great asset to any team."

— Nick Ho Sales Operations Leader, Medidata Solutions

Questions & Answers

1. Who do you work with?
Biotech and pharma companies (early to late stage), CROs, and academic institutions running complex trials. 

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2. How do you charge?
Flexible: project-based (diagnostic + roadmap), day rate for embedded work, or monthly retainer for ongoing advisory. I'll provide a clear scope and fee after our discovery call.

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3. How quickly can you start?
Discovery call within days. Rapid diagnostic typically starts within 1–2 weeks, depending on material availability and team schedules.

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4. Do you work internationally?
Yes—I've worked across North America, Europe, Asia-Pacific, and other regions. I understand multi-regional trial complexities and regulatory pathways.

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5. What if my program is already behind schedule?
That's exactly when to call. I specialize in rapid diagnostics and rescue strategies to stabilize programs and get them back on track.

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6. Can you work with our existing CRO or vendors?
Yes. I often work alongside CROs, providing independent oversight, troubleshooting, or filling gaps in expertise.

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7. Do you replace our internal team?
No—I complement your team. I diagnose, advise, and execute fixes, but decisions stay with your leadership.

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8. What outcomes should I expect?
Clarity on root causes, a prioritized action plan, and hands-on support to stabilize and advance your program. Typical results: fewer amendments, faster site activation, improved enrollment predictability, cleaner data, and submission readiness.

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9. How do I get started?
Book a discovery call. We'll discuss your program, challenges, and timeline. If there's a fit, I'll send a scope and proposal within 48 hours.

GET IN TOUCH

Ready to de-risk your program?

Book a confidential discovery call to discuss your challenges and explore how we can help.

Typical response time: 24–48 hours

©2023 by ABBE Consulting. 

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