Our Facility

Our New Jersey facility reflects our dedication to excellence and compliance.

Designed to meet the highest industry standards, it provides a modern environment for efficient, scalable production.

Key Highlights:

45,000 sq. ft. FDA-registered, cGMP-compliant site.

Our facility is more than just a building—it is the foundation of our clients’ trust, enabling us to produce nutraceuticals at the highest level of quality and compliance.

25,000 sq. ft. warehouse space for secure, efficient storage.

15,000 sq. ft. cleanroom environment for precise and compliant manufacturing.

Strategically located near major airports and seaports, ensuring smooth distribution for both domestic and international markets.

Our Team

Behind ZivaQ Pharma is a team of passionate professionals with over 50 years of combined expertise in pharmaceuticals, regulatory affairs, and chemistry.

Our team brings:

Deep scientific knowledge across all stages of product development.

This unique blend of skills ensures that every project is managed with care, foresight, and uncompromising attention to detail.

We don’t just deliver manufacturing services—we deliver peace of mind.

Hands-on experience navigating complex regulatory environments worldwide.

A culture of innovation, precision, and client-focused collaboration.

Manufacturing Capacity

ZivaQ Pharma is built for scale. Our facility and processes are designed to handle projects of every size, from small pilot runs to large-scale commercial production.

Our capabilities include:

Tablets – Production capacity of up to 10 million units per shift.

This capacity allows us to meet the needs of both emerging brands that require smaller, tailored runs and global companies seeking reliable, high-volume production.

Capsules – Production capacity of up to 11 million units per shift.

Powders – Processing capacity of 15,000 kg per shift.

Liquids – Flexible batch sizes with strict quality and consistency controls.