Clinical Trial Services
safeguarding clinical trial success
Sourcing & logistics for critical study materials fast, compliant and global.
In this section:
explore our Clinical Trial Services
Comparator Sourcing & Procurement
Protocol-specific, cost-effective packaging and labeling solutions that accelerate trial readiness and compliance. by our GMP-certified U.S. facility, we deliver flexible, multi-language capabilities to support global studies efficiently and reliably.
Learn More
Secondary Packaging, Labeling & Kitting
Core Services.
Our framework that enables smoother collaboration, clearer communication, and dependable results for you & your project.
Program Management
find out more
Pharmacovigilance
find out more
Regulatory Compliance
find out more
Quality Assurance
find out more
Supply Chain & Logistics
find out more
-
![Icon of a security badge with a checkmark, a person silhouette, and a shield, indicating security or protection.]()
Trial Integrity
We mitigate risk and control trial costs through rigorous regulatory compliance, consistent supply chain performance and transparent, proven processes—prioritising patient safety by preventing supply errors at every stage.
-
![Icon of a handshake with a network of connected people around it, representing collaboration or partnership.]()
Integrated Partnerships
We reduce lead times through integrated planning and responsive execution, removing unnecessary services, add-ons and terms while working in close partnership to simplify complex processes and create a smoother, more predictable experience.
-
![Outline drawing of two hands holding a diamond gemstone, symbolizing value or luxury.]()
Operational Excellence
We communicate proactively and resolve issues quickly, sharing accountability for trial outcomes and success. By building long-term partnerships—not transactional vendor relationships—we deliver reliable, on-time performance across every project.
-
![Illustration of a test tube with a DNA double helix inside, pills, a molecular structure, and a capsule, representing biomedical research and pharmaceuticals.]()
Pharmacovigilance
In compliance with country-specific PV regulations, we manage spontaneous safety reporting and compliant event capture throughout the CU program lifecycle. Learn more.
-
![Checklist paper with a ribbon badge, indicating certification or approval.]()
Regulatory
Compassionate Use requirements vary by country. Tanner designs CU programs, manages submissions, guides manufacturers through controlled, patient-specific access pathways, and supports scenarios where a product may never receive full commercial authorization. Learn more.
-
![A hand holding a ribbon award with a checkmark in a circle, representing quality or achievement.]()
Medical Affairs
Our team offers scientific and clinical expertise supporting eligibility assessments, HCP engagement, medical inquiry response, and appropriate use of investigational or unapproved products. Learn more.
-
![Icon of a cardboard box with recycling arrows around it, indicating packaging or recycling process.]()
Supply Chain & Logistics
GDP-compliant warehousing, cold chain capabilities, controlled substances handling, and specialty logistics ensure secure delivery of unapproved medicines to sites in high-acuity or resource-restricted environments. Learn more.
-
![Outline of two computer screens, with one showing code and programming symbols.]()
Program Management
A dedicated Program Manager oversees all day-to-day operations, timelines, stakeholder communications, and risk mitigation while our US and EU-based Customer Advocates serve as the primary POC for Tanner customers, pharmacists and physicians.
-
![Illustration of a communication or teamwork cycle with four people, arrows connecting them, and speech bubbles in the center.]()
Program Awareness
We provide guidance on compliant, strategic program awareness to help clinicians, treatment centers and patients effectively discover CU options.
