Secondary packaging & clinical trial kit assembly

Secondary packaging plays a critical role in clinical trial execution. Beyond protecting the product during storage and distribution, it is designed to support protocol compliance, facilitate product handling at clinical sites and ensure the integrity of study operations.

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We develop and manufacture customized secondary packaging solutions tailored to the specific requirements of each study, including patient kits, carton boxes, pouches and other dedicated packaging formats. Our services are adaptable to a wide range of investigational products and study designs, from simple packaging configurations to complex, multi-component kits.

To simplify site management and patient administration, we can assemble complete clinical trial kits incorporating investigational products, comparator drugs, ancillary supplies and study-specific materials. Packaging configurations can also be designed to support blind or double-blind studies while maintaining operational efficiency throughout the supply chain.

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Our capabilities include: 

  • Custom patient kit design and assembly 
  • Cartons, pouches and study-specific packaging formats 
  • Multi-component kit assembly 
  • Packaging solutions for blind and double-blind studies 
  • Integration of investigational products, comparators and ancillary supplies 
  • Flexible solutions adapted to study-specific requirements 

This tailored approach helps ensure smooth study conduct, improved logistics management and enhanced compliance throughout the clinical trial lifecycle.

Clinical labelling: design, printing & GMP application

Accurate and compliant labelling is essential to the successful conduct of clinical trials. Our dedicated clinical labelling team designs, prints and applies labels that provide clear instructions to patients and clinical sites while preserving study requirements and regulatory compliance.

Working within GMP compliant environments, we manage the entire labelling process from concept development through final application, ensuring that each project's specific requirements, including storage conditions and study design constraints, are fully respected. 

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Design & prototyping

We develop tailored labelling solutions adapted to your clinical trial requirements, ensuring ease of use for both clinical site personnel and patients.

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Our design services include: 

  • Custom label and treatment unit design 
  • User friendly layouts to support study compliance 
  • Artwork development and review 
  • Prototype and demonstration kits upon request 
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Printing capabilities

We offer a wide range of label formats to accommodate the needs of global and multicenter clinical studies.
Our printing capabilities support booklet labels containing up to 40 languages, enabling efficient management of international clinical trials.

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Available label types include: 

  • Single-panel labels 
  • Flag labels 
  • Tear-off labels 
  • Standard and blackout labels 
  • Multilingual booklet labels 
  • Expiry date extension labels 
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GMP compliant labelling operations

All labelling activities are performed by trained specialists in dedicated GMP areas, following approved procedures and project-specific documentation.

By combining regulatory expertise, flexible design capabilities and GMP compliant execution, we provide an end-to-end clinical labelling solution that supports the efficient and compliant supply of investigational products worldwide.

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Key services include: 

  • Label artwork and print proof preparation 
  • Label specification and issuance management 
  • Development of project-specific Master Batch Records 
  • GMP compliant labelling and packaging operations 
  • Full traceability and quality control throughout the process 
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