Our packaging, labeling and distribution capabilities
Primary and secondary packaging
Packaging of clinical materials including bottles, blisters, vials and patient kits, tailored to your dosage form, study phase and protocol.
Clinical kit design and assembly
Bespoke kit configurations designed around patient use, ancillaries and trial workflows, including blinded and randomized studies.
In-house labeling
Single-panel and booklet labels, multilingual formats and trial-specific labeling managed under GMP controls and quality assurance oversight.
Cold chain and controlled distribution
Distribution solutions designed to maintain product integrity, including temperature-controlled logistics and direct-to-site delivery.
Why SGS?
As the world's leading testing, inspection and certification company, we combine local clinical supply expertise with a global infrastructure for testing, certification and regulatory compliance. Our packaging, labeling and distribution capabilities are embedded within our wider clinical trial services, allowing you to work with a single, trusted partner from manufacture through to site delivery.
With integrated quality systems, international reach and proven experience supporting complex clinical programs, we help you deliver clinical supplies with confidence – on protocol, on time and in compliance with regional regulatory expectations.
Fully dedicated program manager
Your dedicated SGS PACE program manager provides coordination and milestone review points with the relevant subject matter experts, including:
- An initial clinical development consultancy plan
- Preclinical formulation and bioanalysis (to ensure you are FIH ready)
- Clinical formulation/analysis/manufacturing
- FIH dosing
- Bioanalysis and data analysis and reporting
- Evaluation and optimization of the formulation in clinic, based on human data
- Hybrid FIH including POC in a small patient population
- Phase II clinical development approach and management
Deliver clinical supplies with confidence
- Ensure compliant clinical supplyGMP-controlled processes and quality oversight applied to packaging, labeling and distribution help you meet regulatory expectations across regions.
- Reduce trial delays and riskIntegrated planning, in-house labeling and coordinated logistics help minimize errors, rework and supply interruptions.
- Support complex trial designsWe handle blinded, multi-country and cold chain studies with packaging and labeling solutions aligned to randomization and protocol requirements.
- Protect product qualityPackaging configurations and distribution approaches are selected to support stability, handling requirements and shelf-life performance.
Charles LY WA HOI
We're delighted to unveil this service, aimed at enhancing efficiency and streamlining the clinical development journey for our valued customers.
At SGS, innovation is at the heart of everything we do. This initiative is a testament to our commitment to pioneering solutions that allow our clients to gain competitive advantage.
Bringing an investigational product to patients requires more than manufacturing alone. Clinical supplies must be packaged accurately, labeled correctly and delivered on time, while meeting strict regulatory, quality and protocol requirements. Errors or delays at this stage can disrupt studies, increase risk and impact patient safety.
We support your clinical programs with integrated packaging, labeling and distribution capabilities designed to ensure accuracy, traceability and compliance at every step. As part of our clinical trial services, we manage packaging and supply activities in line with your protocol, stability needs and regional requirements – helping you deliver clinical materials safely and reliably.
