Our Headquarters
Superior U.S. cGMP Facilities for Development and Manufacturing
At our state-of-the-art cGMP headquarters in Cranbury, NJ, Experic offers customized pharmaceutical development, manufacturing, and clinical trial supply solutions. Designed with leading engineering, architectural, and construction partners, our facility is purpose-built to provide flexible and scalable capabilities for a variety of filling, packaging, and labeling needs. We also offer room for expansion to accommodate bespoke manufacturing equipment and processes.
Our fully redundant mechanical systems, including a backup generator, allow for a range of storage conditions and uninterrupted operations, ensuring minimized downtime and optimal product integrity. Nearby, in the same office park, our analytical laboratory supports development activities with testing services, stability studies, and in-process and release testing.
Key Features of Our cGMP Facility
Our Cranbury facility is designed with precision and flexibility, ensuring we can handle every aspect of pharmaceutical manufacturing and clinical trial supply packaging, storage, and distribution. Here’s how we support your product’s life cycle, from first-in-human investigational medicinal products (IMPs) to commercially marketed products:
Advanced Equipment and Processing Technologies
With industry-leading technology from our partner Harro Höfliger, we deploy the latest equipment for:
- Precision filling and handling of cohesive powders and inhalation products
- Spray drying for clinical and commercial-scale needs
- Comprehensive processing, storage, and distribution of controlled room temperature (CRT), refrigerated, and frozen materials
Environmental Monitoring and Security
- Continuous 24/7 environmental monitoring and security ensure product integrity
- Full temperature-controlled storage capabilities
- Redundant systems for uninterrupted operations, minimizing risk and downtime
Transparency and Collaboration — Monitor Your Product in Real Time
At Experic, we value transparency and collaboration. Our facility design includes a viewing corridor, allowing clients to monitor their products in real time as they are being manufactured. This unique feature fosters a collaborative, customer-centric approach to every project, ensuring complete visibility and peace of mind.
Facility Specifications
Our facility has ample space and the latest processing technologies to support every stage of pharmaceutical development and clinical trial supply.
Facility Highlights
- Eight primary processing rooms (Class 100,000)
- Three secondary packaging and assembly rooms
- Controlled environment storage, including:
- Controlled room temperature (15–25 °C)
- Refrigerated (2-8 °C)
- Frozen (-20 °C and -80 °C)
- DEA-controlled substance vault
- 28,000 ft² expansion space for future growth
Customizable and Scalable Space
- Build-to-suit areas for customized solutions and immediate expansion
- Priority access to design, engineering, and architectural services
- On-campus GMP construction resources to support rapid expansions
- Seamless commissioning and support for long lead-time items (HVAC, mechanicals)
- Expansion flexibility for control and monitoring systems
- Dedicated client offices for on-site projects and collaborations
Advanced Equipment for Superior Manufacturing
We deploy the latest technology to ensure precision, quality, and flexibility for every project. Our equipment includes:
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- GEA MOBILE MINOR®
- Buchi B-290
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- Equipment capable of high-shear and low-shear blending for various formulations
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- Harro Höfliger capsule filling machines for high precision
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- Suitable for various formulations, including highly potent drugs
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- Cold and thermo-formed blistering capabilities for diverse product types
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- Advanced bottling equipment with clinical serialization and track-and-trace capabilities
Supporting Every Step of the Product Life Cycle
From clinical trials to commercial production, Experic provides comprehensive support for your product’s entire life cycle. Our facility is equipped to handle a range of pharmaceutical products, from early clinical development to large-scale commercial manufacturing. With flexible expansion capabilities and an expert team on hand, we’re here to meet your project’s evolving needs.
Key Features:
- Real-time environmental monitoring and secure vault storage
- Flexible production rooms for process development and large-scale manufacturing
- Controlled storage for DEA-regulated substances (Schedules II–IV)
Specialist Services
Experic offers bespoke development, manufacturing, and clinical packaging, labeling, storage, and distribution services to meet your product's unique needs.