Experic
2 Clarke Drive
Cranbury, NJ 08512
T: 609.537.4040
E: info@expericservices.com
W: https://expericservices.com/
LinkedIn: https://www.linkedin.com/company/expericservices/
Twitter: https://twitter.com/ExpericServices

 

COMPANY DESCRIPTION

Experic, a contract development and manufacturing organization (CDMO) and clinical trial supply services company, supports every phase of a product’s life cycle from conception to clinical and commercial scale, across a range of dosing and packaging formats. While being a specialized inhalation CDMO, we provide drug product development and manufacturing expertise across a variety of modalities from early phase development to clinical and commercial packaging and labeling. Leveraging our state-of-the-art cGMP facility, we manage global delivery of the highest quality products and services, even for expedited projects, while providing unparalleled knowledge, expertise, and customer service.

FACILITIES

Experic operates two facilities in the US and one in Europe. Our headquarters and cGMP facility located in Cranbury, NJ, offers development, manufacturing, packaging, storage, and clinical trial supply services and has expansion space for bespoke manufacturing solutions. Nearby, Experic’s analytical laboratory provides services for method development and validation, in-process testing, release testing, and stability studies. While in Europe, our new 10,000-sq-ft warehouse space in Ireland will provide secure, monitored storage, and logistics services, including cold storage and re-labeling capabilities, for the rapid and reliable distribution of Investigational Medicinal Products (IMPs) and comparators across Europe.

SERVICES & CAPABILITIES

At Experic, we ensure you receive the exceptional, timely service you deserve. From clinical development to market, our goal is to make outsourcing pharmaceutical process development, manufacturing, packaging, and logistics efficient and worry-free.

Our in-house team — which has decades of experience — provides cost-effective and customized solutions to meet your requirements and timelines. Our robust quality management system complies with industry standards and applicable regulatory requirements.

 Comprehensive Services for Oral Solid Dose (OSD) & Inhalation Products

• Drug Product Formulation
• Spray Drying Services
• Drug Product Process Development
• Clinical and Commercial Scale Manufacturing*
• CMC Regulatory Support
• Analytical Testing Services
• Serialization/Aggregation

Clinical Trial Packaging & Labeling Services for All Product Types

• Sourcing of Packaging, Ancillaries, Comparators, and Comedications
• Primary and Secondary Packaging, Labeling, and Kitting
• Clinical Returns, Reconciliation, and Destruction

Validated & Secure Storage & Global Clinical Logistics

• +15°C to +25°C
• +2°C to +8°C
• -25°C to -15°C
• -40°C to -80°C
• Controlled Substances
• Global Clinical Distribution

Specialized Capabilities

• Best-in-Class Harro Höfliger Filling Equipment
• DPI / Dry Powder Inhalation Product Expertise

ADDITIONAL RESOURCES

Whitepaper – Making Key Decisions for Efficient & Cost-Effective Drug Development Programs 

Whitepaper – From Spray Drying to DP – Managing Particles for Optimal Delivery to the Lungs

Webinar – Constructing a Pharma Development & Manufacturing Project Plan: Steps to Evaluate Risk & Find Efficiencies