Photostability Analysis by ICH Q1B Standards Satisfy ICH Q1B standards with expert photostability testing for your drug product. Photostability studies are performed as part of forced degradation studies, product development, or product investigation and complaint handling. We employ photostability chambers that are temperature-controlled with calibrated UV and visible light sources. These studies are executed based […]
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Evaluate Package Performance with Simulated Distribution Testing Ensure the reliable and safe delivery of your packaged-products to the end user with our laboratory testing services. From primary packages to pallets of finished goods, we help you demonstrate your packaging system’s ability to withstand common transport hazards, such as drops, vibrations, high altitude, temperature changes, and
Simulated Distribution Testing for Effective Product Delivery Packaged products must be able to withstand the typical events associated with manufacture, storage, and distribution without damage. Our expert team applies test methods from both ASTM and ISTA to support a wide variety of supply chain considerations. We offer both testing and certification to streamline your testing
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CCI Testing to Support Product Packaging Employ our container closure integrity (CCI) testing programs to provide accurate, sensitive, and reliable data regarding your product packaging performance. This information enables you to characterize packages and materials, optimize sealing parameters, evaluate package storage temperature impact, replace sterility tests for product stability batches, screen production lots for faulty
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Pace Life Sciences LLC, a central laboratory and contract development and manufacturing organization, received an “overall positive review” from the Food & Drug Administration (FDA) after a comprehensive three-day inspection of its San Germán laboratory’s quality systems and data delivery processes. Read more here.
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Long-standing reputation for robust quality is confirmed as company enters 2024 SAN GERMAN, PR., March 28, 2024 (NEWSWIRE.COM): Pace® Life Sciences, LLC, a full-service FDA-registered central laboratory and contract development and manufacturing organization (CDMO) announced the receipt of an overall positive review from The Food & Drug Administration (FDA), following a three-day general inspection of
Former Whitehouse Analytical Laboratory is Now Part of the Pace® Laboratory Network Minneapolis, MN [March 14, 2024] Pace® Life Sciences, LLC, a contract development, and manufacturing organization (CDMO), announced today that it has acquired the Lebanon, New Jersey laboratory facility (formerly Whitehouse Analytical Laboratories) from Curia, a global contract research, development, and manufacturing (CDMO) company.
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Von Rohr brings over 25 years of experience to company Pace® Life Sciences, a full-service contract development and manufacturing organization (CDMO) and a Division of Pace®, a Science and Technology Company, announced today that Dawn Von Rohr has been named Division President. Von Rohr will be responsible for driving growth and continued innovations within the Pace®
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Analysis Request Form (ARF) – Samples submitted to the laboratory must be accompanied with appropriate labels, documentation, and instructions for testing. The ARF is used to document each sample submission to our laboratory and must accompany the sample shipment. Please submit samples directly to the laboratory that will be performing the testing. Samples are received
Fulfilling Your Clinical Supply Packaging Needs Safeguard your drug product’s quality and delivery to its end user with our trusted clinical packaging, labeling, and kitting services. With our assortment of advanced technologies and manual capabilities, we ensure that your project seamlessly transitions into the clinic. We treat each product with the time and attention it
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