Medivaanta offers advanced formulation and product development solutions designed to meet evolving therapeutic and market needs. Our development process focuses on safety, stability, efficacy, and scalability.
Innovative and stable dosage form development.
Scale-up ready formulations for commercial use.
Compliance with regulatory stability guidelines.
We provide GMP-compliant contract manufacturing services with scalable capacity, ensuring consistent quality and timely delivery across product categories.
Manufacturing aligned with national standards.
Flexible batch sizes for growing brands.
Reliable production timelines and dispatch.
Our quality assurance systems ensure strict control over every stage of manufacturing, guaranteeing product safety, consistency, and compliance.
Continuous monitoring during production.
Comprehensive quality and safety evaluation.
Complete batch records and audit readiness.
Medivaanta provides end-to-end regulatory support to ensure smooth product approvals and compliance with applicable regulatory requirements.
Accurate and compliant regulatory submissions.
Support for licenses and registrations.
Ongoing support for guideline adherence.
Our R&D initiatives are driven by innovation and continuous improvement, aimed at developing better, more effective therapeutic solutions.
Research-based product enhancement.
Validated methods and testing protocols.
We ensure efficient supply chain and logistics management to deliver pharmaceutical products reliably and on schedule.
Optimized stock and demand planning.
Reliable logistics and delivery channels.
Medivaanta offers private labeling solutions that enable pharmaceutical partners to launch products under their own brand identity.
Partner-specific labels and packaging.
Quick turnaround for brand launches.
Our pharmacovigilance services ensure continuous monitoring of drug safety throughout the product lifecycle.
Ongoing adverse event surveillance.
Regulatory-compliant safety reporting.
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