First Choice Bio Inc.
QuickCells.com Inc.

First Choice Bio Inc. QuickCells.com Inc.First Choice Bio Inc. QuickCells.com Inc.First Choice Bio Inc. QuickCells.com Inc.

First Choice Bio Inc.
QuickCells.com Inc.

First Choice Bio Inc. QuickCells.com Inc.First Choice Bio Inc. QuickCells.com Inc.First Choice Bio Inc. QuickCells.com Inc.

Low Reproducibility and Translation in Research? A Revolution is coming!

Low Reproducibility and Translation in Research? A Revolution is coming!Low Reproducibility and Translation in Research? A Revolution is coming!Low Reproducibility and Translation in Research? A Revolution is coming!

Low Reproducibility and Translation in Research? A Revolution is coming!

Low Reproducibility and Translation in Research? A Revolution is coming!Low Reproducibility and Translation in Research? A Revolution is coming!Low Reproducibility and Translation in Research? A Revolution is coming!

About us and our Products:

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History

History

History

  

    

Steering Research From Symptoms Toward Causes


A Better Starting Point for Drug Discovery.


For decades, drug development has often searched for treatments that work across large groups of patients diagnosed with the same disease.

But people with the same diagnosis are not biologically identical.

They differ in their genetics, immune resp

  

    

Steering Research From Symptoms Toward Causes


A Better Starting Point for Drug Discovery.


For decades, drug development has often searched for treatments that work across large groups of patients diagnosed with the same disease.

But people with the same diagnosis are not biologically identical.

They differ in their genetics, immune responses, treatment histories, health conditions and many other measurable biological characteristics. These differences may help explain why one patient responds to a treatment while another does not.


Cancer research makes this challenge especially clear.

A large share of the biological material requested from First Choice Bio supports cancer research. Yet cancer is not one uniform disease, and patients with apparently similar diagnoses may respond very differently to the same treatment.

This raises a fundamental question:


Should research begin with the diagnosis alone, or with a better understanding of the biological differences among the people who share that diagnosis?


First Choice Bio is building its approach around the second possibility.

Instead of treating every donor within a diagnosed population as biologically  

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History

History

   

  

  

 interchangeable, researchers could define smaller and more relevant groups using biomarkers and other donor information.


A treatment that works within one group could then be studied across related groups to understand where it continues to work, where it does not and which biological differences may help explain the outcome.


This d

   

  

  

 interchangeable, researchers could define smaller and more relevant groups using biomarkers and other donor information.


A treatment that works within one group could then be studied across related groups to understand where it continues to work, where it does not and which biological differences may help explain the outcome.


This does not guarantee that a treatment will succeed.


It does provide researchers with a better-understood biological starting point.


First Choice Bio’s role is to make human biological samples more knowable by connecting them with:

  • broader biomarker information;
  • relevant health and treatment history;
  • collection and processing details;
  • repeat collections from the same donor;
  • and the biological context researchers need for their specific question.


The researcher determines which information matters.

First Choice Bio makes that information available and connects it to the biological material used in the investigation.


This can help researchers select samples more deliberately, investigate why results match or differ and preserve information that may help   explain unexpected findings later.   

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History


 

  

Many drug candidates fail because laboratory findings do not reproduce or translate successfully into patients. In some cases, potentially useful treatments may also be abandoned because the biological differences behind mixed results were not sufficiently understood.


Better characterization cannot eliminate biological variability.

But 


 

  

Many drug candidates fail because laboratory findings do not reproduce or translate successfully into patients. In some cases, potentially useful treatments may also be abandoned because the biological differences behind mixed results were not sufficiently understood.


Better characterization cannot eliminate biological variability.

But it can make more of that variability visible, and therefore available for scientific investigation.


Our objective is to help move research beyond observing and managing symptoms and toward investigating disease mechanisms and causes.


First Choice Bio, Inc. is raising capital to establish integrated collection centers and laboratories, beginning in the San Francisco Bay Area.


These centers will connect donor recruitment, biological characterization, sample collection, processing, storage, delivery and repeat-donor information within one operating system.


Better-understood biological starting material may help research ask better questions, interpret results more clearly and move from symptoms toward causes.


We invite you to review our Pitch Deck and Executive Summary, and to join us in building that capability.

Connect with us:

+1-707-333-0902 jan@firstchoicebio.com

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Executive Summary

Steering Research from Symptoms Toward Causes
Human biological starting material connected to deeper donor information, biological context and the longitudinal history.


Prepared August 2026

   

Confidential and forward-looking
This document contains management information and forward-looking assumptions. 

Projections are planning estimates, not guarantees. Scientific performance, customer adoption, donor availability, facility timing and   financing outcomes remain subject to validation.


Investment Overview


First Choice Bio, Inc. (FCBio) is a Delaware C-corporation building an integrated human biological-supply operation for discovery, translational and preclinical research. The company will supply conventional human samples while developing SMART Samples: biological assets connected to deeper donor information, standardized collection and processing records, repository history and, where available, repeat collections from the same donor.

   

The central opportunity

Advanced laboratory models are only as interpretable as the biological material introduced into them. FCBio gives researchers a choice: continue using conventional blind or random samples when appropriate, or select better-understood samples when additional biological context can strengthen design and interpretation.

    

Company:          First Choice Bio, Inc.

Market entry:     Conventional human samples and related services

Differentiation:  SMART Samples and connected donor/asset history

Financing:         $7.5 million seed round


The Problem and FCBio’s Response


Much research still begins with samples for which basic information - such as sex, age, basic health status and collection details - may be known, while other biological differences that can affect an experiment remain unknown. Donor shortages can narrow the choices further.


Random selection may be scientifically appropriate; lack of knowledge is a separate issue.


FCBio integrates donor recruitment, qualification, biological characterization, collection, processing, quality control, repository management, fulfillment and repeat-donor follow-up. Researchers define which information matters and whether selection should be random, matched or specific. FCBio’s role is to preserve and make reliable information available.

· Conventional samples remain available for broad research use.

· SMART Samples add deeper donor information, screening, matching and interpretive context.

· Repeat collections can build longitudinal donor histories.

· Repository and donor-recall decisions are informed by observed RFQs, orders and inventory use.

· AI can support matching and pattern recognition, while the connected operating dataset is built through real collections and customer demand.


Products, Customers and Revenue


Initial offerings include whole blood, bone marrow, apheresis material, separated cells and related frozen products for research use. Target customers include biotechnology and pharmaceutical companies, life-science tools and diagnostic developers, contract research organizations, precision-medicine programs and academic or governmental research institutions.

   

Layered revenue model
Base material + SMART characterization + matching/specificity +   special processing and quality testing + freezing/storage/retrieval +   reserved inventory + delivery + agreed scientific collaboration.


The company will not assume that all material from each donor will be sold. Small-volume or narrowly matched orders may reduce opportunities to combine orders or maximize donor utilization. Each order must therefore remain profitable on its own, and repository inventory must be created under demand-linked rules.


Why the Operating Architecture Matters

    

Conventional supply workflow: A sample and basic donor record

           FCBio intended architecture: The donor, every collection, derivatives, stored aliquots and 

           research requirements remain connected


Conventional supply workflow: Characterization added to existing inventory

          FCBio intended architecture: Donor qualification and demand can influence what is     

          collected, retained and matched

 

Conventional supply workflow: One-time donor relationship

          FCBio intended architecture: Repeat collections create longitudinal biological context

 

Conventional supply workflow: Inventory managed primarily by availability

          FCBio intended architecture: RFQs, fulfillment and utilization inform replenishment and 

          donor recall

 

Conventional supply workflow: Software matching as a feature

          FCBio intended architecture Matching operates on a governed dataset accumulated 

          through collections and orders


Competitors can expand characterization and acquire similar algorithms. FCBio’s opportunity is to compound its advantage through patents, IP and Trademarks, but above all through donor continuity, integrated operations, quality, customer relationships and a connected history of real biological assets and real demand.


Commercial Evidence and Market Context

 

Signal: Historical customers

      Management-reported amount: 130+

            Qualification: Prior distribution and market relationships

 

Signal: Historical sales

      Management-reported amount: $650,000+

            Qualification: Completed distribution activity

 

Signal: Requests for quotation

      Management-reported amount: $4.75 million+\

            Qualification: Demand signal, not booked revenue

 

Signal: Acquisition inquiries

      Management-reported amount: 12

            Qualification: Strategic interest, not a commitment


Market conditions increasingly favor human-relevant research inputs. The FDA’s March 2026 draft guidance for New Approach Methodologies (NAMs) emphasizes context of use, human biological relevance, technical characterization and fit-for-purpose performance. FCBio will not validate customers’ research models; it intends to provide better-characterized, traceable starting material that can support those requirements.


Collection Center 1 and Commercialization


The first San Francisco Bay Area collection center will combine donor operations, collection, instant characterization and laboratory processing, quality control, repository capacity, data systems and fulfillment. It is intended to generate revenue while establishing the reference operating model for further expansion.

1. Re-engage historical customers and convert qualified RFQs.

2. Enter through conventional sample demand and reliable fulfillment.

3. Offer instant SMART characterization and matching when the research question requires it.

4. Measure donor acquisition, order contribution margin, SMART attachment, repository turns and repeat-customer behavior.

5. Expand through frozen products and replicate centers only after Center 1 performance is repeatable.


Financial Plan and Funding

    

$ millions          Year 1        Year 2        Year 3        Year 4        Year 5

 

Revenue            1.544          6.045         18.300        59.700      119.500

Gross profit        0.852          3.416         10.629        35.727        73.540

 EBITDA           (2.265)        (1.515)          1.648        18.321        46.379

 Ending cash     4.631           2.378           1.613          9.803        37.318


FCBio is seeking $7.5 million to fund facility preparation, laboratory equipment, donor recruitment and reimbursement, operational and quality personnel, screening and donor-information systems, repository capacity, AI-supported matching, customer acquisition and operating runway through the center’s commercial ramp.

The reconciled financial model reaches positive EBITDA in Year 3. Year 4 represents a material scale step and must be validated against operating capacity, donor availability, order mix and customer conversion. Projections are conservative management planning assumptions, not guarantees.


Leadership, Governance and Principal Risks

    

Team                                                          Role

Jan (Johannes) Breukers                           Founder and CEO

Sam Vasilevsky, PhD                                 Founder and COO

Kamran Tahamtanzadeh                            Founder and Business Development Officer

Jason Aulenbach                                        Founder and CFO


The five-member advisory board adds life-science, business, automation, AI, CMC, portfolio, licensing and M&A experience. The company plans to add laboratory, donor recruitment, quality, data and commercial personnel through the funding round.


Principal risks


· Donor recruitment, qualification and retention may be slower or more expensive than modeled.

· Customers may adopt SMART services more slowly than projected.

· Narrow matching requirements and repository inventory can reduce material utilization.

· Facility qualification, regulatory interpretation and quality systems may delay launch.

· Larger suppliers may implement limited characterization and matching capabilities.

· The revenue ramp may require more time or capital than the base model assumes.


Investment Conclusion


FCBio’s investment case is a combination of an established market and a differentiated operating model. Conventional samples provide a route to current revenue.

SMART Samples, longitudinal donor relationships and demand-linked repository operations will build a more valuable and increasingly useful infrastructure over time.


The immediate objective is straightforward: finance and launch Center 1, demonstrate disciplined donor and laboratory operations, fulfill customer orders profitably and validate whether better-understood biological assets improve customer decision-making enough to support premium services and repeat demand.


Source / basis: First Choice Bio August 2026 investor presentations; reconciled August 2026 financial model; management-provided commercial and team information; FDA March 2026 draft NAM guidance.

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