Clinical Trial Supply Solutions
Born of Decades of Experience and Expertise
For many years, on both sides of the Atlantic Ocean, Caligor Rx and The Coghlan Group shared the vision of mitigating risks in the clinical trial supply chain—delivering life-saving therapeutics faster to patients in need. In 2017, the two organizations combined, forming CalCog.
For nearly three decades, we’ve dedicated ourselves to supporting innovators’ clinical trial supply chain needs, including clinical packaging and labeling services, kit and label design services, global warehousing and distribution, and comparator and commercial drug sourcing.
We also leverage this expertise to support Expanded Access Program (EAP) design and strategy, program management, and drug supply management services.
With the infrastructure, expertise, and quality management systems of a large clinical supply company and the flexible production schedules and client responsiveness of a small company, CalCog is a key resource for small- and medium-sized pharmaceutical and biotech organizations, as well as CROs.
We are driven to find the best ways to support the clinical packaging and label design, clinical packaging and labeling execution, storage, and distribution needs for each of your clinical trials, often overcoming physical and regulatory barriers and responding to the demands of shifting timelines.
Clinical trial packaging and labeling design strategies that help reduce risk in the R&D supply chain and deliver investigational medication to patients faster.
Quality, compliant, responsive, and on-time secondary packaging and labeling services, including specialized capabilities like ultra-low temperature, wallet cards, just-in-time, and controlled substance packaging services.
Global GMP facilities complemented by comprehensive import/export expertise to ensure your clinical supply chain runs efficiently.
An extensive network of global innovators, wholesalers, and suppliers to meet your comparator, ancillary supplies, and other commercial drug sourcing needs.
The Coghlan Group
Headquartered in the United States, The Coghlan Group offered a responsive source for the preparation, clinical secondary packaging and labeling, and global distribution of clinical trial materials.
Headquartered in the United Kingdom, Caligor Rx offered rich logistical expertise in the movement of clinical trial supplies, specializing in comparator sourcing and Expanded Access Program services.
- US & UK GMP facilities with access to 35+ global depots
- Clinical packaging & labeling design services
- Secondary packaging & labeling services
- Global warehousing & clinical trial logistics
- Clinical trial returns & destruction
- Comparator & commercial drug sourcing
- Early & Expanded Access Program support
- Importation management services
- UK & EU Qualified Person services
CalCog is dedicated to increasing the efficiency and effectiveness of the clinical trial supply chain, helping to speed the delivery of life-changing therapeutic innovations to patients around the world.
CalCog is rooted in critical characteristics that combine to facilitate the success of our clients’ programs.
We understand that program timelines change due to unforeseen upstream delays, and we adapt with them. CalCog’s flexible planning model helps keep your program goals on track.
We know any delay or interruption in the supply chain can impact patient safety and compromise the integrity of your clinical trial. CalCog promptly addresses and manages any delays and challenges.
Clinical trials require significant resources. You can rely on CalCog for transparency from the initial budget to monthly tracking of consumption to overall clinical supply budget management.
Let our experienced team work for you. Each CalCog program team is comprised of industry experts with years of clinical trial supply, expanded access program, comparator sourcing, and ancillary supply sourcing experience.
CalCog commits to a 24-hour response from our program team, and our executive leadership team proactively ensures each program’s objectives are met and client expectations are exceeded.
Clinical supply chain success depends on the involvement of a diverse range of expertise allowing for better decision-making, problem-solving, and study execution. At CalCog, we are here to collaborate with you along your clinical journey.
CalCog is a steering committee-led organization supported by a dynamic team of quality, compliance, operations, and business development professionals. This collaborative approach to corporate leadership has allowed CalCog to be highly flexible and responsive.
Executive Vice President and Chief Business Officer
Kerry is responsible for driving CalCog’s business growth strategy and overseeing CalCog’s commercial, operations, and client services functions. Kerry’s leadership success in industry-leading organizations such as Quest Diagnostics, Allergan, and Pfizer gave her the needed experience and expertise to lead the growth and ongoing success of the CalCog organization.
Executive Vice President and Chief Financial Officer
Matt is responsible for overseeing and managing CalCog’s financial & IT functions and developing and maintaining CalCog’s annual operating plan and budget. Matt’s extensive experience in corporate financial management and leadership allows CalCog, its partners, and suppliers to thrive within a responsibly and effectively managed organization.
Executive Vice President and Chief People Officer
MaryNic is responsible for developing and engaging CalCog’s skilled workforce, optimizing training, professional development, and performance management to support CalCog’s growth. MaryNic is an experienced, passionate human resources professional. Before joining CalCog, MaryNic spent over a decade in human resources in the manufacturing sector and 20+ years as general counsel specializing in ethics and human rights.
Advisory Board Members
Looking for Clinical Trial Supply Services You Can Count On?
Leverage CalCog’s almost three decades of clinical trial packaging, labeling, warehousing, and distribution expertise to advance your clinical trial.