Our Services
Comprehensive regulatory and academic support tailored for healthcare and research professionals.
DHR Registration Support – End-to-end guidance for Ethics Committee registration with the Department of Health Research.
CDSCO Regulatory Support – Documentation preparation, portal submissions, and regulatory query guidance.
Ethics Committee Setup & Compliance – SOPs, logs, forms, archival systems, member documentation, and audit-ready processes.
NABH Documentation Support – Compliance documentation and ethics committee readiness for accreditation audits.
SOP Development & Review – Drafting and updating SOPs aligned with ICMR, ICH-GCP, CDSCO, and NABH standards.
Clinical Research Documentation – Protocol documents, CRFs, study files, and research documentation support.
Research Protocol Preparation – Structured guidance for clinical research protocol development and formatting.
Academic & Thesis Support – Assistance with literature review, research methodology, thesis preparation, and academic submissions.
Regulatory Query Resolution – Professional responses to CDSCO, DHR, and regulatory documentation queries.
Research Compliance Guidance – Support for maintaining compliant and audit-ready research systems.
Our Mission & Commitment
Supporting healthcare and research with clear, compliance-focused guidance tailored for hospitals, investigators, ethics committees, and students.
150+
15
Trusted Partners
Experts
Clinical Regulatory India's guidance made navigating regulatory hurdles surprisingly simple and efficient.
Dr. Mehta
★★★★★
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