Register Now: Beyond EDC: Designing a Connected Data Strategy for Predictive Clinical Development
News|Articles|June 12, 2026

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

Listen
0:00 / 0:00

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.
SHOW MORE

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
  1. 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/

Related to this article

© photon_photo - © photon_photo - stock.adobe.com
Standardized measurement across five oncology centers found that clinical research coordinators rated eSource-enabled workflows positively (Overall Mean Satisfaction 5.79 of 7), with reduced manual entry and electronic data transfer earning strong marks, while perceived reduction in sponsor and monitor queries lagged as the one domain below threshold.
Where the Industry Is Headed as Clinical, Operational, and Real-World Data Connect
In this video interview, Rajneesh Patil, global head of AI, digital, and innovation in clinical development at Syneos Health, describes the industry’s trajectory toward a unified intelligence orchestration environment—and explains why the future isn’t one model that knows everything, but a trusted system that brings the right evidence to the right human decision.
What Expanding AI Ecosystems Mean for Sponsor Complexity and Oversight
In this video interview, Rajneesh Patil, global head of AI, digital, and innovation in clinical development at Syneos Health, argues that CROs must act as orchestrators rather than aggregators—and that the real test of any AI ecosystem is whether it reduces sponsor coordination burden or just hands it back to them.