Category 01
For Students & Admissions
Eligibility, batch timings, hospital site rotations, and placement assistance.
Graduates and post-graduates in Pharmacy (B.Pharm, M.Pharm, Pharm.D), Medicine (MBBS, BDS, BAMS, BHMS, BUMS), Life Sciences (BSc / MSc in Biotechnology, Microbiology, Biochemistry, Zoology, Botany), Nursing, and Physiotherapy (BPT) are eligible to apply. Final year students awaiting final semester results may also register on a provisional basis.
Unlike purely theoretical institutes, Clinovia maintains formal MOUs with 7 multispecialty hospitals in Nagpur. During the second half of the diploma, students spend allocated clinical rotation days shadowing active Clinical Research Coordinators (CRCs) inside hospital research units, learning patient consenting procedures, Investigational Product (IP) cold-chain storage, and trial master filing.
Yes. We offer both Weekday Full-Time batches and Weekend Executive Hybrid cohorts. Weekend cohorts attend live interactive masterclasses on Saturdays and Sundays led by our global and corporate mentors, complemented by flexible virtual lab access and scheduled hospital rotation slots.
We provide complete end-to-end placement support including resume re-engineering, domain-specific technical mock interviews, LinkedIn branding, and direct access to exclusive corporate recruitment events—such as our recent Pool Campus Drive 2026 with Advantmed India LLP.
Category 02
For Pharma, CROs & Hospitals
Site Management Organization (SMO), IEC timelines, and corporate recruitment.
Clinovia manages Phase II to IV interventional drug and device trials, post-marketing observational registries, and comparative efficacy studies. Therapeutic areas covered across our 7 partner hospitals include Oncology, Cardiology, Endocrinology/Diabetes, Rheumatology, Gastroenterology, Dermatology, and AYUSH formulations.
Our affiliated partner hospitals maintain active, CDSCO-registered Institutional Ethics Committees meeting on predictable monthly schedules. Full protocol reviews typically conclude within 3 to 4 weeks from dossier submission, with expedited review pathways available for non-invasive or observational registries.
Yes. We regularly host co-branded recruitment drives (such as the Advantmed India LLP Medical Coding Drive). We manage student sourcing across Central India colleges, conduct preliminary technical aptitude screening, and provide on-site interview and computer lab infrastructure.
Category 03
For Doctors & AYUSH Practitioners
Investigator eligibility, evidence documentation, and medical publishing.
Clinovia operates on a turnkey research coordination model. We assign a dedicated, trained Clinical Research Coordinator (CRC) to your clinic or hospital unit. The CRC handles informed consents, patient scheduling, electronic CRF data entry, and lab tracking. You provide clinical oversight and treatment decisions.
Absolutely. Global medical journals welcome evidence on complementary and traditional medicine, provided the study follows standardized GCP protocols, validated biomarker endpoints, and rigorous statistical analysis. Clinovia's biostatisticians and medical writers specialize in structuring AYUSH studies for international peer review.
Category 04
Regulatory & Compliance Standards
CDSCO, ICH-GCP E6(R2), 21 CFR Part 11, and data privacy.
All training curricula and trial management operations adhere strictly to the Central Drugs Standard Control Organisation (CDSCO) New Drugs and Clinical Trials Rules (2019), the International Council for Harmonisation (ICH) GCP E6(R2) guidelines, ICMR Ethical Guidelines for Biomedical Research, and US FDA 21 CFR Part 11 requirements for electronic records.
Yes. All clinical registries, electronic CRFs, and research archives use pseudonymized subject identification, encrypted cloud data repositories, and role-based access control, complying with India's Digital Personal Data Protection (DPDP) Act and HIPAA standards.
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Our academic counsellors and clinical coordinators are available to answer your specific queries.