Clinical Research & Clinical Trials
Site Management Organization (SMO) services, protocol development, trial coordination, ethics committee compliance, and patient recruitment across partner multispecialty hospitals.
Advancing Research. Transforming Healthcare.
Bridging Academia, Clinical Research & Global Healthcare Innovation
Clinovia Research & Innovations LLP is a quality-driven clinical research, healthcare services management, and academic organization committed to delivering high-quality, ethical, and evidence-based solutions across the healthcare, research, and education ecosystems.
7 Multispecialty Corporate Hospitals collaborations for Clinical trials — and number is growing
25+ Globally and Nationally Renowned Faculty Members from Industry
ICH-GCP & CDSCO Compliance
Clinical Trials | Pharmacovigilance | CDM | Education | Training
Dedicated to Excellence in Clinical Research, Safety, Data & Education
CIN: Registered LLP
Standard: ICH-GCP E6(R2)
Collaborations: 7 Multispecialty Hospitals
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Corporate Hospital Collaborations (Growing)
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Globally & Nationally Renowned Faculty
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Advance Diploma Programs
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Students & Clinicians Trained
The RIDET Foundation
Our Holistic Methodology
The core philosophy powering our clinical solutions and educational programs.
R
Research
I
Innovation
D
Data Mgmt
E
Education
T
Training
Comprehensive Solutions
What We Do
Providing end-to-end clinical research support, workforce upskilling, regulatory documentation, and healthcare data integrity.
Professional Courses & Training
Advance Diploma programs in Clinical Research, Pharmacovigilance, CDM, and Medical Coding delivered online and offline with real hospital exposure and placement assistance.
Clinical Data Management (CDM)
Electronic Data Capture (EDC) design, case report forms (eCRF), discrepancy management, medical coding reconciliation, database lock, and audit-ready data-quality assurance.
Pharmacovigilance & Drug Safety
Comprehensive Adverse Event (AE) / Serious Adverse Event (SAE) management, ICSR processing, narrative writing, signal detection, and regulatory safety reports.
Medical Coding & Billing
Expert ICD-10-CM, CPT, and HCPCS coding services, clinical chart audit, medical record abstraction, documentation review, and revenue cycle claims management.
Medical Writing & Scientific Communication
Authoring Clinical Study Reports (CSRs), clinical protocols, Investigator Brochures (IB), systematic literature reviews, biostatistics, and peer-reviewed journal manuscript publishing.
Our Educational Philosophy
Discover the Clinovia Difference
Learn. Apply. Innovate. Grow.
Most training institutes stop at classroom certificates. At Clinovia, our students train directly within real clinical research sites and multispecialty corporate hospitals.
1
Learn
Master ICH-GCP, regulatory guidelines, and modern software tools from global corporate experts.
2
Apply
Experience real trial coordination, patient consent, and CRF documentation across 7 partner hospitals.
3
Innovate
Engage in evidence synthesis, research analytics, and protocol optimization methodologies.
4
Grow
Graduate as an industry-ready professional directly hireable by global CROs and pharma companies.
Live clinical trial site execution & hospital floor coordination at our partner multispecialty centers in Nagpur.
Key Differentiators
Why Clinovia
How our integrated research and training model sets a new standard for clinical education and industry collaboration.
01
Research Site to Training Ecosystem
We operate active clinical research trial sites ourselves. Training isn't theoretical; students learn on the exact infrastructure where trials take place.
02
Industry-Ready, Not Certificate-Ready
Curriculum focused on operational competencies, trial audits, software navigation, and regulatory compliance that companies test during hiring.
03
Real-World Exposure from Global Faculty
Learn directly from seasoned leaders working inside top multinational corporations including TCS, IQVIA, Novartis, and international research universities.
04
Deployment at Clinical Research Sites
Formal MOUs with 7 multispecialty corporate hospitals provide guaranteed on-site rotations, investigator shadowing, and live trial participation.
05
Talent Pipeline for Pharma & CROs
We serve as a verified recruitment hub, hosting pool campus drives (e.g. Advantmed India) to place qualified life science and medical graduates.
Our Process Line
Our Evidence-Driven Approach
A rigorous 4-stage pipeline translating scientific curiosity into tangible clinical transformation.
1. Research
Identification of clinical gaps, protocol formulation, feasibility assessment, and regulatory approval planning.
2. Evidence
Patient recruitment, standardized data capture, GCP trial monitoring, and biostatistical verification.
3. Innovation
Integration of electronic data management, AI-assisted coding, and modernized study workflows.
4. Impact
Peer-reviewed publications, therapeutic validations, improved clinician practices, and superior patient care.
Strategic Direction
Our Vision
To emerge as a trusted global platform for clinical research, professional education, healthcare innovation, and evidence generation — recognized for uncompromising scientific rigor and human-centered healthcare advancement.
Our Commitment
Our Mission
To advance scientific research, develop skilled healthcare professionals, enable high-quality clinical research, and deliver innovative evidence-based solutions that contribute to better healthcare outcomes and therapeutic excellence.
25+ Globally & Nationally Renowned Faculty Members from Industry
Learn from Renowned Industry Leaders
Our honorary academic advisors bring extensive expertise and experience from leading multinational pharmaceutical companies, premier CROs, and internationally recognized research institutions.
Mr. Akash Dhokne
GermanyClinical Research Professional
Dr. Vishal Pendharkar
Cambridge, UKDrug Discovery Leader & Research Scientist
Mr. Onkar Rathod
Glenmark PharmaceuticalsDy. GM – Clinical Research & Regulatory
Mr. Chetan Ingale
TCSGeneral Manager (Pharmacovigilance)
Mr. Adarsh Sharma
IQVIASr. GM – Clinical Trials & Global Operations
Mr. Rahul Dhamat
NovartisSr. Manager – Clinical Data Management
Irene Uclés
Barcelona, SpainCRA – Early Clinical Development
Jasmina Deisting
GermanyCRA & Certified EU Clinical Trials Project Manager
Client & Student Feedback
Reviews & Testimonials for Our Services
Insights from life science graduates, clinicians, and partner hospital coordinators collaborating with Clinovia.
Connect With Us
Start Your Research Career or Partner with Clinovia
Whether you are a student exploring Advance Diplomas, a clinician aiming to publish, or a pharmaceutical sponsor seeking trial sites in Central India, our experts are here to assist.
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Nagpur Headquarters
Clinovia Research & Innovations LLP
Wardha Road, Medical Corridor, Nagpur, Maharashtra 440015, India -
Phone Support
+91 712 299 8877 -
Official Email
contact@clinovia.in
Operating Hours: Monday – Saturday, 9:30 AM – 6:30 PM IST
Request Consultation or Information
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