Products and Pricing
First in Human efficacy data at a fixed price
VC Ready. Proof of Concept. Fixed Scope. Agreed Timelines.
Who are these products addressed to?
B
Biotech startups
M
Medical Device companies
P
Big Pharma new drugs
V
Investment Funds, Venture Capital Companies
U
Universities R&D
Core Products Price List
The following SaaPs Packages cover the core operational execution of the trial.
The studies are performed in ONE COUNTRY ONLY, at Tigermed EMEA selection, fully compliant with the FDA/EMA requirements.
Timelines are depending on the protocols.
- MedTech Velocity
- $ 545,000
-
15-20 Subjects
SSU: 6-7 months Timeline: Depends on the protocol.
Standardized early-phase trial for medical devices (non-implantable).
Delivers full Feasibility/Pilot data.
- Pharma Genesis
- $ 645,000
-
18-22 Subjects
SSU: 6-7 months Timeline: Depends on the protocol.
First-in-Human program for small molecules or biologics.
Phase 1a (SAD Only).
- Cardio Sprint
- $ 645,000
-
16-20 Subjects
SSU: 6-7 months Timeline: Depends on the protocol.
Accelerated First-in-Human trial for cardiovascular innovation
Cardiovascular Phase 1a (SAD Only).
- Neuro Synapse
- $ 695,000
-
16-20 Subjects
SSU: 6-7 months Timeline: Depends on the protocol.
Early-stage evaluation for neurological therapeutics.
Neuro Phase 1a (SAD Only).
- Onco Discovery
- $ 795,000
-
20-24 Subjects
SSU: 6-7 months Timeline: Depends on the protocol.
Oncology-focused First-in-Human clinical trial.
Full Dose Escalation
Should your indication or approach not be encapsulated by our product packages above, we will curate a specific fixed price within the price points above that is specific to your trial.
There are no limitations on indication or phase that we can manage.
Complete Your Mission
Essential Add-On Packs
To ensure true budget transparency and scientific rigor, we offer some standardized add-on packs.
These eliminate the “hidden costs” of traditional CRO contracts by bundling essential exclusions into fixed prices.
- The Regulatory Architect
- $ 45,000
-
Medical Writing & Preparations
Study Protocol development
(Standardized Template)Investigator Brochure (IB)
review/refinement
- The Data Core
- $ 65,000
-
Clinflash or similar (No Medidata)
EDC (Electronic Data Capture) Setup & Licensing
eCRF Design (Standard Library
design)
Scope of Work
and Pricing Framework
Included in the Core Product Price
The following core services are included in our fixed-price model:
Feasibility: Initial assessment of study design, patient availability, and site capability.
Regulatory Start-up: Submission of clinical trial applications (CTA) and ethics approvals.
Site Contracting: Negotiation and execution of agreements.
Project Management: Full oversight and coordination of timelines, communication and status reporting.
Site Monitoring: Continuous supervision of site performance and protocol compliance.
Data Management & Statistics: GDPR and Data Transfer compliant collection, validation, analysis, and reporting of study data. (Open Source EDC – i.e. OpenClinica)
Labor Work Site Fees: Compensation for investigator sites.
NOT Included in the Core Product Price
The following items are excluded from the base price:
Medical Writing (See “The Regulatory Architect” Add-On).
Systems & Platforms (See “The Data Core” Add-On).
Laboratory/Clinical Services: variable cost
Vendor Management: Third-party vendor fees outside the standard ecosystem.
Patient Travel/Reimbursement: Billed at cost
Insurance: variable cost
Payment Schedule
For the 6 core products:
4 installments:
- Up-front payment (50%)
- Ethical Comitee EC and Competent Authority CA approval (20%)
- 100% subjects recruited (20%)
- Trial Master File TMF delivery (10%)
Insurance to be paid upfront.
For Pass-Through Costs
- Up-front payment (20%)
- Monthly payments upon trial kick-off
For Add-On Packages
- "The Regulatory Architect" - 2 installments of 50%
- "The Data Core" - Payment upfront
in partnership with
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