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Services >> Clinical Trial Material, Packaging & Logistics >> Secondary Packaging & Labeling

Secondary Packaging & Labeling

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Tailored Clinical Packaging and Labeling for Your Trials

Eurofins CDMO (Contract Development & Manufacturing Organization) network of companies takes pride in offering an extensive array of services for clinical supply manufacturing and management. With a focus on accelerating time-to-market for (bio)pharmaceutical companies, we understand the criticality of efficient and customized clinical packaging and labeling. Our expertise extends to phase I, II, and III studies for both sterile and non-sterile dosage forms, including blisters & blister-cards, bottles, pre-filled syringes (PFS) and pens, medical devices, infusion kits, and small packaging vials. We provide a wide range of label types, such as single panel, tear-off, black-out, flag, and booklet labels, ensuring the perfect fit for your unique clinical trial design.

Optimizing Clinical Trial Supply Management

At Eurofins CDMO, our experienced project manager team collaborates closely with you to design the optimal patient kit according to your protocol. We understand that efficient clinical trial supply management is vital to the success of your trials, and we go the extra mile to handle various additional activities with precision and care. Our services include randomization list creation, text translation, comparator sourcing, double-blinding, ancillary kits management (perfusion materials), leaflet printing, and more. With our seamless approach to clinical trial supply management, you can focus on your research, knowing that every aspect of packaging and labeling is in expert hands.

Partner with Eurofins CDMO for Streamlined Clinical Trial Supply

When it comes to clinical trial packaging and labeling, Eurofins CDMO is your reliable partner. Our comprehensive range of services and expertise in clinical supply manufacturing ensures that your trials run smoothly and efficiently. From designing patient kits to handling complex logistical challenges, we are committed to meeting your specific needs and timelines. Our dedication to excellence and attention to detail make us a preferred choice for (bio)pharmaceutical companies seeking streamlined clinical trial supply management.

Elevate Your Clinical Trials with Eurofins CDMO

Ready to experience seamless clinical supply manufacturing and management for your clinical trials? Choose Eurofins CDMO as your partner and unlock the full potential of your research. Our expert team is here to guide you every step of the way, ensuring that your clinical packaging and labeling align perfectly with your trial design. Fill in the contact form below to get started on your journey towards efficient clinical trial supply management.

 

 

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