ABOUT EXPERIC
Experic is a contract development and manufacturing organization (CDMO) and clinical trial supply services company dedicated to revolutionizing pharmaceutical development, manufacturing, and clinical trial supply. Established in 2018, Experic offers a comprehensive suite of services, including process development, analytical and formulation development, clinical and commercial manufacturing, and clinical packaging and logistics. Specializing in challenging powders and inhalation products, our expertise encompasses tablets, pellets, capsules, and low-dose dry powder inhalation therapies.
Operating from our state-of-the-art, Class A cGMP facility in Cranbury, New Jersey, we manage the global delivery of high-quality products, even for expedited projects. Our team of industry leaders brings decades of experience in pharmaceutical product development and clinical trial supplies, ensuring strategic vision and execution for every project.
At Experic, we are committed to delivering innovative, client-focused services that accelerate the development and commercialization of life-changing therapies. Our flexible, customer-oriented approach addresses the growing needs of the biopharmaceutical industry, making us a trusted partner in bringing innovative products to market.
INDUSTRY INSIGHTS
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Manual assembly plays a vital role in early‑phase combination product development. Learn how strong process design, collaboration, and quality controls help teams reduce risk, improve consistency, and move confidently toward later‑stage manufacturing.
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Coordinated expertise, real‑time visibility, and clear communication support smoother development, manufacturing, and clinical supply. Strong alignment improves predictability and lowers risk.
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Efficient analytical development speeds decisions and improves risk visibility. Using QbD, digital tools, and strong communication helps teams accelerate timelines while maintaining rigor.
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Rising trial complexity demands agile supply built on integrated operations, solid planning, and fast issue resolution. Lean teams gain from partners providing flexibility, control, and global reach.
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Advanced cGMP facilities deliver control, expertise, and reliable processes that protect quality and support smooth progress to market. Strong partnerships help reduce risk in complex programs.
CONTACT INFORMATION
Experic
2 Clarke Drive
Cranbury, NJ 08512
UNITED STATES
Phone: 609 537 4040
Contact: Antonino Fiorica
SOLUTIONS
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Flexible primary and secondary packaging supports efficient shifts from clinical trials to commercial supply, with scalable infrastructure and expert teams ensuring compliant, reliable solutions.
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End-to-end development, manufacturing, packaging, and logistics streamline complex drug programs and support efficient progress from formulation to global clinical supply.
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Integrated analytical, manufacturing, packaging, and distribution capabilities streamline development and supply. Broad expertise and flexible services reduce handoffs and support efficient progress.