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Our R&D Pipeline

Discover our robust scientific pipeline. Dhanova Healthcare is dedicated to developing high-quality, innovative formulations across General Medicine, Neurology, and Cardiovascular Care to meet critical patient needs.

Discovery Phase
Phase 0

Discovery & Preclinical

Target identification and extensive laboratory testing. Evaluating new chemical entities (NCEs) for initial safety, stability, and therapeutic efficacy in cell models.

Phase I
Phase I

Safety & Dosage

First-in-human testing conducting safety assessments on small groups of healthy volunteers. Focuses primarily on tolerability, pharmacokinetics, and safe dosing scales.

Phase II
Phase II

Therapeutic Efficacy

Testing the drug on a larger cohort of patient volunteers suffering from specific conditions (e.g., Hypertension, Chronic Neuropathy) to validate clinical performance.

Phase III
Phase III

Comparative Studies

Large-scale multi-centric trials to confirm therapeutic benefit, monitor side effects in diverse populations, and compare efficiency against standard existing treatments.

Regulatory Filing
Filing Stage

Regulatory Approval

Submission of comprehensive technical dossiers and New Drug Applications (NDA) to regulatory authorities like DCGI for review and marketing authorization permissions.

Phase IV
Market Release

Post-Market Monitoring

Continuous pharmacovigilance and surveillance after commercial rollout to evaluate long-term safe usability, drug interactions, and optimizing production scales.