Excelion Research CRO Platform
Clinical research (CRO) website presenting trial services and global compliance to pharma sponsors.
Project snapshot
Excelion Research is an international Contract Research Organization (CRO) headquartered in India, delivering clinical trials, bioanalytical studies, and regulatory submission support for global pharmaceutical and biotechnology innovators. Visionite Tech built a website that shows Excelion's trial network, therapeutic breadth and regulatory experience (CDSCO, US FDA, EMA).
- Our role
- Clinical Research Portal, Trial Feasibility & Regulatory Showcase
- Client
- Excelion Research
- Industry
- Life Sciences
- Year
- 2024
Tech stack
Next.js
TypeScript
Tailwind CSS
Vercel
The story
From challenge to result
- 01
The challenge
Global pharmaceutical sponsors and clinical investigators require verified audit metrics, therapeutic area capacity, clinical site readiness data, and Indian regulatory approval roadmaps before committing to multi-million dollar trial programs.
- 02
Our approach
We organized the site around the therapeutic areas, clinical site infrastructure and bioanalytical laboratories that sponsors ask about first. The design puts regulatory compliance front and center.
- 03
The results
- Showcases 250+ clinical trials supported across therapeutic areas
- Showcased 30% faster Indian clinical trial regulatory approval pathways for international sponsors
- Supports outreach to sponsors from North American and European biotech firms
- Built for accessibility, with responsive typography and fast page loads for sponsors worldwide
Features
What we built
Global sponsors see every Excelion service and compliance standard at a glance.
Seven Service Divisions, One Clear Map
Site management, GCP audits, monitoring, regulatory, pharmacovigilance, biostatistics and system validation, each with its own profile and proof points.
Global Compliance Framework
Clear coverage of USFDA, EMA, CDSCO, WHO and MHRA requirements, so sponsors see audit readiness at a glance.
Sponsor Feasibility Questionnaire
Confidential protocol feasibility intake funnel enabling global sponsors to rapidly evaluate site capacity.
Regulatory Approval Desk
A dedicated profile for structured global approval processes, from submission planning to sign-off.
What the client says
“Sponsors judge a research partner in minutes. Visionite gave each of our seven divisions a clear profile and put our USFDA, EMA and CDSCO readiness front and centre.”
Viral SavaliyaClinical research, Excelion ResearchStart a project
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