Expertise, Reliability, and Strategic Advantage in Worldwide Distribution
When it comes to the global shipment of clinical trial materials, Corealis Pharma stands as a beacon of excellence and reliability. With an unwavering commitment to precision, timeliness, and regulatory compliance, we have earned our reputation as a leading partner for biotechnology and biopharma companies seeking seamless Oral Solid Dose (OSD) formulation development, GMP production and hassle-free shipping to clinical sites across continents.
Unmatched Global Capabilities
Corealis Pharma orchestrates global deliveries of clinical trial materials with exceptional efficiency. By applying our proven logistics infrastructure we consistently ship weekly – without issue – to major clinical trial destinations including Australia, the United States, Canada, and Europe. Notably, Corealis Pharma’s clinical trial material shipments remain unaffected by the U.S. tariff concerns as outlined in the prototyping exemption under subheading 9817.85.01 of the Harmonized Tariff Schedule of the U.S. (HTSUS). Count on your U.S. deliveries to be tariff-free. Whether your project demands rapid deployment across multiple clinical sites or careful coordination of sensitive drug products, our experienced team ensures your clinical trial materials reach their destination safely and on schedule, every time.
Strategic Relationships and Regulatory Expertise
Our longstanding and robust relationships with trusted customs brokers are key to our seamless international shipping operations. By leveraging these partnerships, Corealis Pharma skillfully navigates the complexities of cross-border shipments, minimizing delays and ensuring strict adherence to regulatory requirements worldwide.
For shipments within North America, we streamline your supply chain further by leveraging coverage under the USMCA (United States-Mexico-Canada) free trade agreement and the HTSUS exemption, as mentioned above ensuring duty-free deliveries. This not only facilitates smooth and cost-effective movement of materials across the continent, but also ensures compliance with evolving trade regulations and remaining unaffected by recent trade tariff implications.
Access to Critical Materials for Drug Development
Corealis Pharma’s strategic location in Quebec, Canada, provides unrivaled access to APIs (Active Pharmaceutical Ingredients) and all other materials essential for the development and manufacturing of GMP drug products ready for clinical trials. Our established sourcing networks and proximity to leading suppliers allow us to rapidly procure and deploy critical components, accelerating your project timelines and boosting overall productivity.
We acknowledge effective management and storage of clinical supplies is a critical component of clinical operations. To address this need, Corealis offers a range of clinical material packaging services, including blisters, bottling, and pouching. Additionally, we specialize in blind or double-blind packaging, ensuring the integrity and reliability of the trials.
Corealis also excels in patient kit preparation, meticulously assembling the necessary materials for trial participants. Their clinical supplies management services encompass warehousing, distribution, and reconciliation, ensuring that all clinical materials are handled with the utmost care and precision.
Decades of Experience and Proven Track Record
With a legacy rooted in excellence, Corealis Pharma brings decades of experience to every shipment. Our highly skilled logistics professionals understand the unique challenges of global clinical trial product distribution and are adept at managing every detail, from documentation and customs clearance to specialized packaging and temperature control. We have successfully supported over 700 clinical trials across 28 countries for clients ranging from emerging biotechs to global pharmaceutical leaders.
- Weekly, reliable shipments to Australia, the United States, Canada, and Europe
- Strong, enduring relationships with customs brokers for smooth border crossings
- USMCA coverage & HTSUS exemption for simplified North American shipments.
- Immediate access to APIs from various countries and GMP materials
- Deep expertise in regulatory compliance and logistics coordination
Choose Reliability. Choose Corealis Pharma.
When you partner with Corealis Pharma, you gain far more than an Oral Solid Dose development and manufacturing provider, you gain a committed ally with the expertise, infrastructure, and global reach to ensure your clinical trial materials are where they need to be, exactly when they need to be there. Experience the reliability that comes from working with a team that anticipates challenges, solves problems, and delivers excellence at every step.
Reach out to Corealis Pharma today and propel your clinical development forward with the assurance of world-class logistics and global distribution expertise.
For inquiries, please contact:
Patrick Frankham, VP Business Development
Corealis Pharma Inc.
Email: patrick.frankham@corealispharma.com
Phone: +1 (450) 973-7505
www.corealispharma.com
Contact Corealis
Corealis’ experts are ready to answer any queries about the company’s oral solid dose offering, including its development and manufacturing capabilities.
