Our Approach
Our Commitment to Quality, Collaboration, and Transparency
At Experic, we don’t just follow a quality system, we embody it as a shared responsibility and a fundamental part of our identity. Our unique commitment to quality, collaboration, and transparency sets us apart, ensuring that every project we undertake meets the highest industry standards, from development to manufacturing and clinical trial supplies.
A Comprehensive Approach to Quality Management
Our quality management system (QMS) is designed with flexibility and scalable rigor, ensuring compliance with global regulations. We follow industry-leading practices and current good manufacturing practice (cGMP) guidelines to maintain inspection readiness at all times. From our standard operating procedures (SOPs) to ongoing employee training, every aspect of our operations is structured to meet the most stringent quality and regulatory requirements.
Key Compliance Standards:
- U.S. FDA: 21 CFR Parts 210, 211, 820, and more
- ICH Standards: Q7, Q9, Q10
- EU GMP: EudraLex Volume 4 guidelines
- ISO 13485:2016
- DEA Schedules I–V Compliance
We prioritize continuous improvement and innovation, ensuring our QMS evolves alongside emerging regulations and technologies to support your product’s success at every phase.
Collaboration That Drives Success
At Experic, collaboration is at the heart of how we work. We understand that developing and manufacturing pharmaceutical products requires teamwork, transparency, and communication. That’s why we’ve designed our processes to keep you informed and involved.
How We Collaborate
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We align our goals with yours, working together to meet project milestones and exceed regulatory expectations.
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Our customers can monitor their products in real-time during manufacturing and packaging, ensuring complete visibility.
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Each project is managed by a dedicated team that serves as your advocate, ensuring seamless communication and timely updates.
Transparency in Action
At Experic, we believe in complete transparency. Whether it’s the real-time monitoring of your product’s manufacturing or open communication about regulatory challenges, we ensure you’re always in the loop.
Our facility’s design allows clients to actively participate in the process, with viewing corridors for real-time observation of manufacturing. This approach reflects our core values of trust, openness, and customer service.
Commitment to Customer Service and Compliance
Quality isn’t just about meeting regulatory standards — it’s about exceeding customer expectations. At Experic, we strive to deliver high-quality, safe, and effective products and services on time, every time. Our commitment to customer satisfaction drives everything we do, from our meticulous product quality to responsive, customer-focused service.
Why Choose Experic for Quality
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Our QMS ensures full compliance with U.S. FDA, DEA, and international standards for controlled substances, drug products, and medical devices.
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We refine our processes and systems to improve quality outcomes and efficiency.
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Continuous training ensures our team stays at the cutting edge of industry practices and innovations.
A Proven Commitment to Quality and Regulatory Compliance
Experic is fully registered with the U.S. FDA and holds a manufacturer registration with the U.S. Drug Enforcement Administration (DEA) for Schedule I through Schedule V Controlled Drug Substances. Additionally, we maintain a certificate of registration for drug and medical devices with the New Jersey Department of Health, ensuring the highest regulatory compliance standards.
Our quality policy is simple: to deliver products and services that exceed customer expectations every time. We continuously monitor performance and enhance our systems to maintain these high standards.
Specialist Services
Experic offers bespoke development, manufacturing, and clinical packaging, labeling, storage, and distribution services to meet your product's unique needs.