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 Nagpur-based, technology-driven organization delivering advanced clinical research training, trials management, and evidence-based solutions for students, clinicians, pharma, and hospitals.
7 Partner Multispecialty Hospitals
14+ Global & National Faculty
ICH-GCP & CDSCO Compliance
Nagpur-Based Clinical Research, Site Network Management & Healthcare Innovation Hub
CIN: Registered LLP
Standard: ICH-GCP E6(R2)
Sites: 7 Nagpur Hospitals
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Partner Hospitals (MOUs)
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Int'l & National 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.
Global Faculty Network
Learn from Renowned Industry Leaders
Our advisory and teaching faculty brings rich experience from multinational pharma leaders, premier CROs, and international research institutes.
Mr. Chetan Ingale
TCSGeneral Manager (Pharmacovigilance)
Mr. Adarsh Sharma
IQVIASr. GM – Clinical Trials & Global Operations
Mr. Rahul Dhamat
NovartisSr. Manager – Clinical Data Management
Dr. Vishal Pendharkar
Cambridge, UKDrug Discovery Leader & Research Scientist
Kate Savenko
UkraineExpert – Clinical Data Management & EDC
Iva Sabeva
BulgariaClinical Research Coordinator
Irene Uclés
Barcelona, SpainCRA – Early Clinical Development
Jasmina Deisting
GermanyCRA & Certified EU Clinical Trials Project Manager
Student & Partner Voices
What Our Community Says
Insights from life science graduates, clinicians, and partner hospital coordinators trained at Clinovia.
Got Questions?
Frequently Asked Questions
Find answers regarding our courses, hospital internships, corporate SMO capabilities, and placement assistance.
Our programs are open to graduates and postgraduates from Pharmacy (B.Pharm, M.Pharm, Pharm.D), Medicine (MBBS, BDS, BAMS, BHMS, BUMS), Nursing, Physiotherapy, Biotechnology, and Life Science disciplines.
Through our active MOUs with 7 multispecialty corporate hospitals in Nagpur, enrolled candidates participate in site rotations, learning trial coordination, patient consent documentation, eCRF logging, and GCP monitoring firsthand.
Yes! We offer flexible weekend and weekday hybrid cohorts. Theory lectures and software sessions are hosted interactively online, while hands-on clinical rotations are coordinated on-site.
We provide complete site feasibility, Principal Investigator (PI) liaison, institutional ethics committee (IEC) submissions, clinical study coordinators (CRCs), patient recruitment, and certified CDM/Safety reporting.
We train clinicians to become GCP-compliant Principal Investigators, design scientific clinical trials around their therapies, and publish observational or interventional studies in indexed international medical journals.
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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Headquarters
Clinovia Research & Innovations LLP,
[Building / Floor Name], [Street / Area],
Nagpur, Maharashtra, [PIN CODE], India -
Phone Support
+91 98765 43210 (Template Placeholder) -
Official Email
info@clinovia.example.com (Template Placeholder)
Operating Hours: Monday – Saturday, 9:30 AM – 6:30 PM IST
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