GMP & Compliance Services

GMP Repackaging & Labelling

Your trusted partner for comprehensive clinical packaging and labelling solutions.

With over 10 years of experience in clinical trial repackaging and labelling, and operations across four strategic locations in Europe, we bring proven expertise and regional agility to every project. Our dedicated teams ensure that your IMPs, NIMPs, and ancillary supplies are handled with precision—fully compliant, clearly labelled, and ready for smooth trial execution.

GMP Repackaging – Tailored Secondary Packaging Solutions for Clinical Trial Integrity

Ensure the integrity and readiness of your clinical trial materials with PHOENIX CTS’s GMP Repackaging Services—designed for precision, compliance, and flexibility. We transform finished medicinal products into trial-ready formats—customized to your protocol, country requirements, and patient needs. Whether assembling patient kits, site kits, or multi-country batches, our GMP-compliant processes and dedicated teams guarantee accuracy, traceability, and speed.

With over 10 years of experience and four strategic locations across Europe, we’re equipped to support your clinical trial logistics with agility and confidence.

Secondary Repackaging Services

Repackaging of finished medicinal products into trial-specific formats

Assembly of patient kits, site kits, and country-specific kits

Inclusion of IMPs, NIMPs, and ancillary items

Temperature-Controlled Packaging

Cold chain packaging under GMP conditions

Integration of temperature monitoring devices

Packaging operations under ambient (15°c-25°c), refrigerated (-2°c - -8°c) and frozen conditions (-20°c)

Labelling – Expert Clinical Labelling Services You Can Trust

Ensure clarity, compliance, and confidence with PHOENIX CTS’s GMP-compliant clinical labelling solutions. We specialize in designing, printing, and applying labels tailored to your trial’s specific needs—whether for IMPs, NIMPs, or ancillary items. From multi-language booklet labels to tamper-evident and temperature-sensitive formats, our services support both global and country-specific requirements.

Our dedicated teams, together with a network of qualified partners, work with precision and speed, offering just-in-time labelling, variable data printing, and full traceability—so your products are always trial-ready and regulatory-compliant.

GMP Labelling Services

Design, printing, and application of compliant clinical labels
Multi-language booklet labels and variable data printing
Tamper-evident and temperature-sensitive labelling
Just-in-time labelling for adaptive trials or late-stage customization

Blinding & Over-Labelling

Blinding of comparator products
Over-labeling for protocol-specific requirements [Comment: Consider using 'over-labelling' for consistency with British English spelling.]
Rescue medication labelling

Regulatory & Translation Support

Label text translation and regulatory review
Country-specific compliance checks
Support for CTA submissions and packaging documentation

Return & Destruction

Managing unused or expired clinical trial materials doesn’t have to be complex with the support of PHOENIX Clinical Trial Services (CTS). Our GMP-compliant returns and destruction services ensure that your Investigational Medicinal Products (IMPs), Non-Investigational Medicinal Products (NIMPs), and ancillary items are handled with full traceability, regulatory compliance, and environmental responsibility.

We coordinate secure returns from trial sites, oversee certified destruction through qualified vendors, and—where applicable—support the re-sale of unused stock to help you recover value and reduce waste. With experienced teams and a trusted European network, we offer a seamless, transparent process that protects your study’s integrity and optimizes your supply chain.

Certified Destruction Services

Destruction of expired, damaged, or unused clinical trial materials
Execution through qualified and licensed vendors
Full documentation and certificates of destruction
Environmentally responsible disposal methods
Compliance with local and international regulatory requirements

Re-Sale of Unused Stock

Identification of eligible products and suitable markets based on regulatory and commercial criteria
Utilization of our own established wholesaler network across Europe to explore re-sale options and meet local
Collaboration with qualified partners to ensure compliant and secure redistribution
Value recovery through sustainable solutions that reduce waste and optimize inventory

By incorporating our GMP Labeling & IMP Repackaging services into a larger suite of solutions, PHOENIX streamlines your clinical trial supply chain, increasing operational efficiency, reducing turnaround times, and thus enhancing overall productivity. This integrated strategy eases the logistical challenges related to IMP preparation, freeing our partners to focus more on the critical aspects of their clinical research.

Power up Your Clinical Journey!

PHOENIX is ready to support your clinical trials, navigating the complex demands and tight schedules of today's pharmaceutical domain.