Maiva Pharma - Pharma. Made Better.

Maiva Pharma

Pharma. Made Better.

Over 1 Billion vials Delivered

US FDA & EU GMP Approved

Committed to Global Health

Pharma. Made Better.

Maiva Pharma is a trusted global CMO/CDMO with over three decades of expertise in sterile injectable manufacturing. Our US FDA-approved, state-of-the-art facility delivers end-to-end contract development and manufacturing solutions, from formulation to commercial production, ensuring precision, safety, and regulatory excellence. With certifications from US FDA, EU GMP, ANVISA (Brazil), Health Canada, and PIC/S, Maiva Pharma consistently meets the highest global quality standards. Our expert team provides customized, scalable solutions designed to accelerate product development and time-to-market. At Maiva Pharma, we go beyond manufacturing — we create trusted partnerships built on reliability, innovation, and integrity, helping our clients bring life-saving therapies to patients worldwide.
Maiva Pharma — Precision. Reliability. Partnership.

Our Services

CDMO

We providing end-to-end pharmaceutical development and manufacturing solutions with a focus on quality, compliance, and innovation.

CMO

Offering reliable and scalable pharmaceutical manufacturing services tailored to your product and market needs.

Maiva Innovation

Creating high-quality, market-ready products in-house and licensing them to trusted global partners.

Maiva Custom Feature Block

Maiva Innovation

Our in-house R&D creates ready-to-license pharmaceutical products. We focus on innovation, quality, and regulatory excellence. Empowering partners to expand their portfolio faster.

Scale Up & Tech Transfer

We ensure seamless technology and site transfer through structured planning and validation. Our expert team manages every step from process adaptation to regulatory compliance.

Stability Studies

We offer comprehensive stability study services. Equipped with controlled chambers for long-term, accelerated, and intermediate conditions. Ensuring product quality, safety, and efficacy throughout its shelf life.

Regulatory Support

Comprehensive dossier preparation support for global regulatory filings. We ensure all technical, analytical, and compliance data meet submission standards. Helping you achieve faster approvals with confidence.

Contact Us

For more information contact us directly on our email ID

Regulatory Approvals

European Union's Good Manufacturing Practices Approved

Brazilian Health Regulatory Agency (ANVISA)

Contact Us:
No 32, Sipcot Industrial Complex,
Phase I, Hosur, Krishnagiri,
Tamil Nadu, 635 126
India

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