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Experic

Specialist powder-handling CDMO with integrated development, manufacturing, and packaging services.

Specialist powder-handling CDMO offering clinical trial supply, development, manufacturing, and packaging services for pharmaceutical products. Headquartered in United States.

Development & manufacturing

Structured CDMO capabilities from verified public sources.

Synthetic chemistry infrastructure

Capabilities
DEA licensed

Fill-finish formats

Regulatory clearances

Services

About this organization

Experic is a contract development and manufacturing organization (CDMO) specializing in powder-handling capabilities. The company provides integrated services across the pharmaceutical development and manufacturing lifecycle, including process development, analytical development, formulation development, clinical manufacturing, commercial manufacturing, dry powder inhalation, clinical trial supply, packaging and labeling, clinical storage and logistics, and specialty manufacturing.

The organization operates with a quality management system (QMS) designed for flexibility and scalable rigor, ensuring compliance with global regulations including U.S. FDA 21 CFR Parts 210, 211, 820, ICH Standards (Q7, Q9, Q10), EU GMP (EudraLex Volume 4), ISO 13485:2016, and DEA Schedules I–V. Experic emphasizes collaboration, transparency, and real-time customer visibility during manufacturing and packaging operations, with dedicated project management teams serving as customer advocates.

Certifications

AuthorityIdentifierSource
FDA21 CFR Parts 210, 211, 820View
ICHQ7, Q9, Q10View
EMAEudraLex Volume 4View
ISO13485:2016View
DEASchedules I–VView

Locations

  • US Facility

    United States

  • EU Facility

    European Union

  • EU Facility

    Europe

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