20
May
2025
Avema Contract Servies
Exhibitor at CPHI Americas 2025 stand 816
About Us
Categories
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US
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2017On CPHI since
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1Certificates
Company types
Event information
CPHI Americas 2025
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20 May 2025 - 22 May 2025
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Pennsylvania Convention Center, Philadelphia
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Visit us at stand 816
Products Featured at CPHI Americas 2025
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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... -
Product Formulation Development
Avéma has an extensive library of formulations and more than 40 years of Rx formulation development experience. -
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... -
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. -
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 ... -
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... -
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. -
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... -
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... -
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...
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