QuVa Pharma


QuVa Pharma is a leading FDA-registered 503B outsourcing facility specializing in high-quality sterile compounding. The company is committed to providing reliable, safe, and compliant compounded medications to healthcare facilities across the United States. With a focus on quality, safety, and regulatory adherence, QuVa Pharma supports hospitals and health systems in addressing drug shortages, reducing costs, and improving patient care through its extensive portfolio of ready-to-administer sterile products and innovative manufacturing capabilities.

Industries

health-care
manufacturing
medical
medical-device
pharmaceutical

Nr. of Employees

large (251-1000)

QuVa Pharma

Sugar Land, Texas, United States, North America


Patents

Ready to use liquid formulation

US-11642308-B2

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Ready to use liquid formulation

US-10952962-B1

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Ready to use liquid RECK formulation

US-10952963-B2

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Products

Prefilled syringes (non-opioid periarticular injection formulation)

Ready-to-administer prefilled syringe formulation intended for periarticular injection in surgical settings to reduce opioid use.

Buffered lidocaine + epinephrine prefilled syringes

Ready-to-administer buffered local anesthetic prefilled syringes intended to simplify local anesthesia preparation and use.

Topical gels and solution ready-to-administer products

Ready-to-use topical gels and solution formulations supplied in standardized packaging for clinical use.

Dextrose prefilled syringe offering for shortage response

Prefilled dextrose syringes produced to address critical shortages and restore supply to hospital customers during supply disruptions.


Services

Batch production and supply of ready-to-administer sterile injectables and other compounded sterile preparations for hospitals and health systems under 503B regulatory framework.

Formulation, development, scale-up and technical support for novel sterile drug products intended for hospital use, including support for patenting and commercial launch.

Data-driven supplier resiliency scoring and dashboards that combine upstream manufacturer, CMO and API source signals with contracting and inventory data to predict supply risk.

Analytical and microbiological testing to support release, stability programs, and regulatory compliance for compounded sterile products.

Consultative assessments to align product portfolios, compounding strategies, and inventory planning with hospital clinical needs and regulatory requirements.

Expertise Areas

  • Sterile compounding and compounded sterile product (CSP) manufacturing
  • cGMP pharmaceutical manufacturing and FDA 503B compliance
  • Supply chain resiliency and drug shortage response
  • Stability testing and beyond-use date (BUD) extension
  • Show More (4)

Key Technologies

  • Aseptic/sterile compounding
  • cGMP manufacturing systems
  • ISO-class cleanroom engineering (primary engineering controls, RABS)
  • Stability testing and stability-indicating assays
  • Show More (5)

News & Updates

Partnerships with Leading Hospitals

QuVa Pharma partners with major health systems to provide reliable sterile compounded medications, supporting clinical needs and drug shortage mitigation.

Expansion of Manufacturing Capacity

The company has added significant new space and capabilities, including 44,000 sq ft of 3PL space and increased BUDs, to enhance supply resilience.

Industry Leadership in Quality and Safety

QuVa Pharma is recognized for its adherence to cGMP standards, FDA compliance, and innovative manufacturing practices.

Addressing Drug Shortages with 503B Outsourcing

QuVa Pharma plays a critical role in mitigating drug shortages by providing ready-to-use sterile medications and developing new formulations.

The Future of Hospital Pharmacy Supply Chains

The company emphasizes proactive strategies, technological advances, and strong partnerships to ensure continuous medication supply.

Regulatory Updates and Industry Standards

QuVa Pharma stays at the forefront of compliance with evolving USP and FDA regulations, supporting hospitals in maintaining high standards.

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