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Central Safety Lab

Home / Central Safety Lab
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Central Safety Lab

Home / Central Safety Lab
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Welcome to the QPS Central Safety Lab: Your Trusted Partner for Safety Testing in Clinical Trials

At the QPS Central Safety Lab, we specialize in providing comprehensive safety testing services tailored specifically for small and mid-sized pharmaceutical and biotech clients across the United States. Our mission is to streamline and support your clinical trials by managing every aspect of safety testing, allowing you to focus on what matters most: advancing your research.

What We Do

Our service offers a full suite of safety lab testing solutions, ensuring that your clinical trials are compliant, accurate, and efficient. From sample collection to lab testing, we handle it all. We understand that safety testing is critical in clinical research, and our experienced team ensures your trials proceed smoothly with the highest standards of accuracy and compliance.

All-Inclusive Testing Services

Through these diverse tests, the QPS Central Safety Lab provides comprehensive safety monitoring, ensuring that all potential risks are identified and addressed throughout the clinical trial process. We provide an all-encompassing range of safety testing services, including:
  • Hematology and biochemistry analysis, which assess blood and organ function to detect potential adverse reactions to investigational drugs.
  • Immunogenicity testing to evaluate whether a patient's immune system is producing antibodies in response to the treatment
  • Urinalysis, hematology, toxicology, biochemistry, serology, and female health testing that play key roles in monitoring how the drug behaves in the body over time.

Full Service, Zero Hassle

One of the key advantages of partnering with QPS Central Safety Lab is our commitment to handling all aspects of the testing process for you, including:
  • Shipping: We manage all logistics, ensuring that test kits (hyperlink to Clinical Trial Kit page) are shipped directly to your sites, on time and without delay.
  • Kit Contents: Each test kit is fully equipped with everything needed for sample collection, ensuring there are no gaps or uncertainties during the collection and testing process.
  • Order Management: We take care of the ordering and delivery process, freeing up your time and resources so you can focus on the clinical trial conduct.

Why Choose the QPS Central Safety Lab?

Our service offers a full suite of safety lab testing solutions, ensuring that your clinical trials are compliant, accurate, and efficient. From sample collection to lab testing, we handle it all. We understand that safety testing is critical in clinical research, and our experienced team ensures your trials proceed smoothly with the highest standards of accuracy and compliance.

Focus on Trials:

By taking care of all logistics, shipping, and kit contents, we allow you to focus your energy on the important aspects of your trial — improving efficiency and reducing your workload.

Simplified Process: :

With our all-inclusive service, there’s no need for you to manage multiple vendors or services. We handle the entire safety lab testing process for you, from ordering to reporting. Using the QPS Central Safety Lab significantly simplifies the clinical trial process by consolidating all safety testing needs into a single, streamlined service. With us managing every aspect—from sample collection and testing to shipping and kit contents—you eliminate the complexities of coordinating multiple vendors or handling intricate logistics.

Our all-in-one approach ensures that test kits are delivered on time and with all necessary components, allowing your clinical team to focus on the critical elements of the trial, such as data collection. By taking care of the administrative and operational tasks, we reduce your workload, improve efficiency, and ensure a smoother trial experience, ultimately accelerating the path to valuable insights and successful outcomes.

Quality and Compliance:

Our services are designed to meet the highest industry standards for quality, compliance, and accuracy, ensuring your clinical trials remain in full regulatory adherence. At the QPS Central Safety Lab, we place the highest priority on maintaining stringent quality and compliance standards across all of our services. Our lab operations adhere to the latest industry regulations, including Good Clinical Practice (GCP) and College of American Pathologists/Clinical Laboratory Improvement Amendments (CAP/CLIA) ensuring that every test is conducted with precision and in full alignment with regulatory guidelines.

Our experienced team employs state-of-the-art technologies and robust quality control procedures to guarantee accurate, reliable results that meet the highest standards of safety and integrity. By consistently delivering high-quality data, we help our clients maintain the trust of regulatory bodies and ensure their clinical trials progress smoothly, with full confidence in the safety and efficacy of their products.

Focused on Small to Mid-Size Biotechs and Pharmaceutical Companies

For small biotech companies, navigating the complexities of safety testing during clinical trials can be particularly challenging. The QPS Central Safety Lab offers a tailored solution that allows these companies to streamline their processes without the need for large-scale infrastructure. By providing comprehensive testing services, including shipping, kit contents, and order management, we eliminate the burden of logistics and administration. This enables small biotech firms to focus their time and resources on innovation and trial progression, rather than managing the intricacies of safety lab operations. With a cost-effective and scalable approach, Central Safety Lab ensures that your clinical trials are safe, compliant, and efficient, helping you advance your groundbreaking therapies with confidence.

The QPS Central Safety Lab also understands the unique needs of mid-sized pharmaceutical companies. Our flexible, scalable solutions are designed to support growing organizations without the complexity or cost associated with larger safety testing providers. Whether you’re running a small, early-phase trial or a larger-scale study, we provide the expertise and resources to ensure your safety testing needs are met.

Links to Relevant Documents

  • Efficiently Performing Two Global Approval Studies in Prostate Cancer Patients
  • Phase II-IV Clinical Overview
  • Phase II-IV Clinical Services & Locations
  • Early Phase Clinical Overview
  • Expedited Study Delivery – Logistics
  • Expedited Study Delivery – Pharmacy
  • Studying Sedatives in Phase I Studies
  • Pharmacokinetic Studies in Patients
  • Corporate Overview Clinical Sites

Testimonials

Thank you very much for delivering the QC’ed data by timeline. It is great to work with you and your team.
LEI L.
Thank you again for the very nice draft report.
KAREN V.

Time is of the essence in Drug Development.

Contact the QPS Business Development Team Today!

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Clinical Services

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  • Early Phase Clinical Trials
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Headquarters Location

Delaware Technology Park,
3 Innovation Way,
Newark, DE 19711

  • +1 512 350 2827
  • +1 302 369 5602
  • info@qps.com

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