News|Articles|June 12, 2026

PLPS Launches MyClinicalSuite™ to Deliver Faster Clinical Trial Label Turnarounds Without Compromising Quality, Compliance, or Patient Safety

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Key Takeaways

Dedicated clinical-only production segregates trial work from commercial runs, minimizing queue conflicts and helping protect study milestones under compressed timelines.
Accelerated labeling is positioned alongside patient safety and compliance requirements, using robust quality systems to reduce operational and regulatory risk.
Operational features include flexible order sizing, real-time specialist support, and built-in scheduling/accuracy controls to accommodate late-stage protocol-driven changes.
In-house variable data printing and in-line vision inspection with 200% verification validate barcodes and human-readable content to support accurate patient control and administration.
An ISO-certified Lakewood, NJ cGMP facility supports extended content, cryogenic, and pattern-adhesive labels, expanding capabilities across regulated pharma, device, OTC, and specialty packaging.

Premium Label & Packaging Solutions launched MyClinicalSuite™, a clinical-dedicated label and packaging environment that segregates trial work from commercial production to accelerate timelines while maintaining regulatory compliance and data integrity.

Clinical trial sponsors face constant pressure to accelerate study timelines while maintaining strict regulatory compliance and data integrity. As trial designs become more complex and schedules continue to compress, even small delays in label production can impact critical study milestones.¹

To help sponsors meet these challenges, Premium Label & Packaging Solutions (PLPS) has launched MyClinicalSuite™, a clinical-only label and packaging environment that segregates clinical work from commercial production. Because projects don’t compete with commercial runs, its resources are completely focused on maintaining the highest standards of quality, compliance, and data integrity while providing faster turnaround times.

Speed without compromise

Although quick turnarounds are important, clinical trial labels require more than just quick production. Every label must support patient safety, study integrity, and regulatory compliance. MyClinicalSuite™ was developed with the realities of today's trial protocols in mind. By combining advanced production capabilities, industry expertise, and robust quality systems, we’re able to provide accelerated timelines while reducing operational and regulatory risk.

Key advantages of MyClinicalSuite™

Order size flexibility so that large or small batches are treated equally, regardless of size
A responsive team of specialists to provide answers in real time
Built-in accuracy and scheduling so late-stage changes can be executed flawlessly while adhering to timelines
In-house variable data printing to support accurate patient control
In-line vision inspection to ensure quality and secure clinical trial administration

The MyClinicalSuite™ portfolio offers a wide range of clinical trial labels and packaging applications, including booklets, extended content, and specialty labels such as cryogenic and pattern-adhesive. They are manufactured at PLPS's ISO-certified Lakewood, New Jersey facility, which has been producing clinical trial labels and packaging since 2008. The plant follows strict cGMP standards and features Integrated vision systems and 200% inspection processes that can validate both barcodes and human-readable data.

The launch of MyClinicalSuite™ further expands PLPS’s broader healthcare capabilities in pharmaceutical, medical device, OTC, and regulated healthcare markets across pressure sensitive labels, expanded content labels, shrink sleeves, flexible packaging, and specialty packaging applications.

Reference

PLPS Launches MyClinicalSuite™ to Deliver Faster Clinical Trial Label Turnarounds Without Compromising Quality, Compliance, or Patient Safety. News release. PLPS. Accessed June 12, 2026. https://premiumlabelandpackaging.com/myclinicalsuitelaunch/

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