Experic, LLC
About Experic, LLC
Certifications
Categories
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US
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2020On CPHI since
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2Certificates
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50 - 99Employees
Company types
Primary activities
Products from Experic, LLC (4)
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Product Process Development and Support Services
Experic offers a consultative and collaborative approach to technical transfer, formulation, and process development based on a foundation of deep scientific knowledge, the ability to solve problems, and facilitate scale-up. Process development activities are augmented with expert technical project mana... -
Product Clinical Trial Supply Services
Experic provides comprehensive solutions to support clinical trials from study planning to close-out, including clinical trial supply management services, commercial drug sourcing, and clinical-scale manufacturing services. Manufacturing services include powder blending; powder, pellet, or tablet fil... -
Product Specialty Commercial Manufacturing Solutions
Experic provides a variety of services to support Phase 3 to commercial-scale process transitions to create a customized solution for your specialty, niche, orphan, or combination product. Build-to-suit dedicated suites, a flexible solution available for immediate expansion, enable us to customize... -
Product Analytical Services
With a team of experienced scientists and a robust toolbox of analytical techniques and equipment, Experic can support the life cycle of your oral solid dose and/or inhalation pharmaceutical products. Our laboratory staff provides comprehensive analytical solutions to support the formulation, development, ...
Experic, LLC Resources (2)
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News Enhanced Protection for Manufacturing Highly Potent Pharmaceuticals Introduced at New Jersey Facility
Experic Expands Capabilities to Manufacture Highly Potent Drug Products -
Whitepaper Making Key Decisions for Efficient and Cost-Effective Biopharmaceutical Drug Development Programs
In today’s biopharmaceutical landscape, financial markets are tighter while speed to market remains a critical factor when making development decisions. Increasingly, biopharmaceutical companies are having to make tough choices when prioritizing development of investigational products in their pipelines. Working with a contract development and manufacturing organization (CDMO), however, can help stakeholders ensure that the design of a product’s development program is efficient and appropriate for the stage/phase of development. This article will address how a biopharmaceutical company can leverage the collaborative efforts with their CMDO partner to understand the implications of certain key development decisions. We will also discuss a few types of decisions companies may want to avoid which may preserve cash or reduce costs in the short term but can have unwelcome effects later.
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