Your Clinical Trial Partner

Streamlined clinical
trials, powered by data.

By leveraging the world's largest clinical trial dataset, we streamline clinical trial design — and match you with the right partner from our 20,000+ global life science service provider network.

730,000+
Clinical trial records

20,000+
Global life science service providers

AI-powered
Protocol curation engine
Company

Your clinical trial partner —
from first idea to final protocol.

MEDIAIPLUS turns the world's largest clinical trial dataset into clear decisions. We streamline trial design and connect you with the right partner from a 20,000+ global life science service provider network — breaking bottlenecks to drive a virtuous cycle in clinical trials.

What drives us

A single decision surface
for clinical trials.

Scattered intelligence, brought into one place — so your experts spend their time on judgement, not legwork.

01

Data, not guesswork

Every recommendation is grounded in 730,000+ clinical trial records and 1.2M+ FDA records — the world's largest clinical trial dataset.

02

The right partner, faster

A curated network of 20,000+ CROs, CDMOs, SMOs, and Tech/AI vendors, matched to your trial objectives in days — not weeks.

03

AI that does the heavy lifting

Curation and drafting that cut labor-intensive prep time, without cutting rigor or traceability.

Testimonials

Why they chose MEDIAIPLUS.

Operators and partners across pharma, biotech, and government on what changed after working with us.

I'm happy to pay for more CRO information. Until now I've relied on my personal network, but it had its limitations. MEDIAIPLUS offers a much broader and more reliable resource.

Dom Messerli CEO · LENOSSS MEDICAL

MEDIAIPLUS's team and service is revolutionary. Many clients have lost money searching for a CRO only to find it's not a good fit. MEDIAIPLUS's network of global CROs will help you complete your goals anywhere in the world.

Sean Yoshikawa CEO · Decoto International

MEDIAIPLUS's network of over 29,000 CROs is extensive. Collaboration with the Belgian biotech industry is already underway, and we look forward to seeing even more global partnerships in the future.

Adrien Lacroix Trade & Investment Counsellor · Embassy of Belgium
Solution 01 · FiCRO

Match with the right life science partner.

FiCRO connects you with the right partner from a curated network of 20,000+ life science service providers — CROs, CDMOs, SMOs, and Tech/AI vendors — matched to your trial objectives.

FiCRO FiCRO partner matching dashboard
The old way was hard

Finding the right partner through analog channels takes weeks — and often misses fit.

Our network spans every therapeutic area and region. Submit your trial parameters once and FiCRO narrows the field for you, with verified capability records and direct introductions from our team.

  • 20,000+ vetted CROs, CDMOs, SMOs, and Tech/AI vendors
  • Filter by therapeutic area, modality, region, and scale
  • Direct introductions from the MEDIAIPLUS team
Solution 02 · MediC

AI-powered clinical trial curation.

Access all protocol design essentials in one place: drugs, diseases, modalities, guidelines, similar trials, and competing drugs.

MediC MediC clinical trial intelligence dashboard
Trial intelligence

"MediC has drastically reduced the time spent on labor-intensive tasks."

— Life Sciences Professional, CSO Tarik S. Chaudhry

Bring drugs, diseases, modalities, guidelines, and similar trials into one workspace, and let AI surface what matters for your next protocol.

  • One-click access to 730,000+ clinical trial records
  • Side-by-side competitor and guideline review
  • Drugs, diseases, modalities, and similar-trial lookups in one workspace
Solution 03 · MedidraftAI

From product idea to protocol draft in 10 minutes.

MedidraftAI analyzes 730,000+ clinical trial records to recommend a regulatory path, benchmark similar devices, and auto-generate an evidence-based protocol draft — complete with source citations.

MedidraftAI MedidraftAI protocol drafting workspace
Trial preparation

Cut weeks of protocol prep down to a single afternoon.

Built on a RAG architecture over 730,000+ clinical trials and 1.2M+ FDA records, MedidraftAI handles the labor-intensive groundwork — so your experts can focus on the judgement calls that actually move the trial forward.

  • Regulatory path matching: 510(k), PMA, De Novo
  • Similar-device benchmarking and approval probability
  • ICH-GCP–ready protocol drafts with full source traceability
Literature review
4 weeks 1 hour
Protocol draft
8 weeks 3 days
Solution 04 · MediScholar NEW

MediScholar — an evidence-grounded research copilot.

Clinical evidence is scattered across trial registries, literature, patents, and guidelines. MediScholar unifies them into a single knowledge graph and drafts a purpose-aligned report — where every claim, number, and conclusion traces back to its source.

MediScholar MediScholar — evidence report, live knowledge graph, and analytics dashboard
Knowledge-graph RAG

From a question to a cited, review-ready draft.

MediScholar's KG-RAG engine interprets your intent, searches the connected sources, and cross-checks every statement against the original before assembling a structured draft. Passages that need human judgment — off-label use, dosing, regulatory interpretation — are flagged for expert review rather than stated as fact.

  • Hybrid retrieval — BM25 + dense vector search, re-ranked by a biomedical cross-encoder
  • Self-correcting drafts (CRAG) — unsupported claims removed before you ever see them
  • Trust-tiered, fully cited output with inline source traceability
  • Domain adapters — oncology, medical-device & patent landscapes, competitor and patent-expiry monitoring
Try MediScholar
By the Numbers

Breaking bottlenecks to drive
a virtuous cycle in clinical trials.

Clinical trials are complicated and challenging. Delays in development can result in significant financial loss. MEDIAIPLUS turns scattered intelligence into a single decision surface.

730,000+
Clinical trial records (as of Jun 2025)
20,000+
Global life science service providers
100%
Focus on clinical trial intelligence
Get Started

Take the first step toward
a successful clinical trial.

Tell us about your pipeline and the trials you're planning. We'll come back to you within a working day.

Contact Us