28
Oct
2025

Avema Pharma Solutions

Exhibitor at CPHI Frankfurt 2025 stand 4.1L1, Contract Manufacturing and Services
About Us

Avéma Pharma Solutions is a true CDMO for Rx and OTC supporting your product from concept to commercialization. We develop and manufacture oral liquid dose and solid dose units, including: suspensions, solutions, tablets and capsules. Delivery technologies include:

  • immediate release systems,
  • modified release systems, 
  • delayed-release and extended-release, 
  • chewable tablets,
  • quick dissolve tablets,
  • two-piece hard-shell capsules and taste masking, 
  • extended release using
...

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  • US
  • 2017
    On CPHI since
  • 1
    Certificates
Company types
Contract Service
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Event information
CPHI Frankfurt 2025
  • 28 Oct 2025 - 30 Oct 2025
  • Messe, Frankfurt
  • Visit us at stand 4.1L1, Contract Manufacturing and Services

Products Featured at CPHI Frankfurt 2025

  • Commercial Manufacturing

    Product Commercial Manufacturing

    Covering a 135,000ft² area, our Miami facility is registered with the FDA and complies fully with current good manufacturing practice (cGMP) guidelines. It has the capacity for R&D, process development and small-scale launches, including pilot-scale cGMP manufacturing and packaging to support pilot pharmac...
  • Formulation Development

    Product Formulation Development

    Avéma has an extensive library of formulations and more than 40 years of Rx formulation development experience.
  • Gummy Manufacturing

    Product Gummy Manufacturing

    Avéma Pharma Solutions and PL Developments has responded to the increasing demand for gummies by adding gummy manufacturing capabilities, including a small line for R&D and scale up, as well as four additional commercial lines with an anticipated capacity of 1.2bn gummies annually. Commercially available p...
  • Laboratory & Analytical Services

    Product Laboratory & Analytical Services

    Avéma has a full analytical lab, staffed by experienced professionals with more than 200 years of method development and validation experience.
  • Packaging & Serialization

    Product Packaging & Serialization

    Avéma can help you improve patient compliance with innovative packaging solutions for solid and liquid dose productions. Our facilities offer flexibility to accommodate run size and interchangeable tooling for line flexibility and cost efficiency – so, we can provide support for all products at all stages ...
  • Pilot Scale Manufacturiing

    Product Pilot Scale Manufacturiing

    To ensure the seamless transition from pilot manufacturing, Avéma starts with small-scale production equipment in the development process that has identical operational attributes to what will be used in full-scale commercial manufacturing all under the supervision of a single project manager to ensure tha...
  • Regulatory Support

    Product Regulatory Support

    Avéma Pharma Solutions can help guide your product successfully through NDA, ANDA, CBE 30 and 505(b)(2) filings with the FDA.
  • Solid & Liquid Dose Drug Manufacturing & Development

    Product Solid & Liquid Dose Drug Manufacturing & Development

    From OTC and Rx to diagnostics and dietary supplements, Avéma manufactures a full range of solid and liquid dose products, all manufactured under strict FDA guidelines and cGMP compliance. With an ever-growing portfolio of innovative formulas and a diverse mix of state-of-the-art equipment, our offerings a...
  • Research & Development

    Product Research & Development

    Avéma offers formulation, process and analytical development support of new or existing products using the most current and effective active ingredients and delivery systems. Our team of scientists bring decades of pre-formulation development expertise to your products, combined with the knowledge of how t...
  • ANDA and NDA Technical Support

    Product ANDA and NDA Technical Support

    As part of its commitment to full service support, Avéma Contract Services is pleased to offer our customers support with ANDA and NDA applications, including bio equivalency studies, collecting background data, supervising technology tranfers and reviewing applications to make sure that companies com...