Quality Control Solutions
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Designed For Inhalation: Pulmonary And Nasal Delivery
Our newly expanded in-house capabilities span clinical and commercial scale manufacturing for DPIs, unit-dose, bi-dose and preserved multi-dose nasal sprays.
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Biopharmaceutical Isolators And RABS
6/14/2023
Ensuring Aseptic Conditions and Containment in Pharmaceutical Industry Processes.
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Feasibility Studies For Container Closure Integrity Testing Applications
7/9/2020
PTI Inspection Systems are scientific instruments being deployed for high risk packaging applications. The environments in which these systems operate is often highly regulated with test results having a significant impact on operational decisions. The reliability and sensitivity of a CCI test method is critical to assure that correct decisions are made to maintain product quality and patient safety. If PTI’s equipment is going to test your packaging, we aim to deliver the most effective solution. Feasibility studies offer a detailed glimpse into the technological capabilities ahead of critical purchasing decisions. Feasibility studies can also act as a preliminary test method for an application. The results from feasibility or method development testing can be rolled out to the production environment for rapid validation and deployment.
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Pharmaceutical Stainless Steel Glovebox For Cytotoxic Drug Development
4/3/2019
Stainlees Steel Glovebox for Cytotoxic Drug Development designed to provide personnel protection while working with powder substances.
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Powder Rheology Accessory
4/6/2023
The Powder Rheology Accessory expands the DHR’s capabilities to powders, enabling the characterization of behaviors during storage, dispensing, processing, and end-use.
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Thermal Analyzers For The Most Demanding Biopharma Applications
5/17/2023
Measure heat flow, weight loss, dimension change, or mechanical properties as a function of temperature.
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API/HPAPI Containment Solutions For Pharmaceutical Manufacturing
3/27/2019
Solve your containment challenge by working with a company that understands your process, CPT, expectations, facility allowances and restrictions as well as specific equipment specifications.
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HPAPI Package Inspection Enclosure
3/26/2019
The HPAPI Package Inspection Suite is designed to provide personnel and product protection down to a respiratory exposure of at least 100 micrograms per cubic meter air (100 ug/m3). Package inspection operations involve manipulation of highly potent pharmaceutical ingredients (HPAPI), such as fentanyl.
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Biologics Quality Control: A Critical Component Of Development And Production
Quality control is a critical component for ensuring safety, efficacy, and consistency in the development and production of biologics. This comprehensive list of strategies, techniques, workflows, and best-in-class products for developing biopharmaceuticals can help you navigate the complexities of biologics and simplify the manufacturing process. Improve your quality control procedures and optimize your biologics production process with tools and expertise relied upon by researchers worldwide.
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R&D And Analytical Services
3/4/2022
Our team of analytical experts provides experience, efficiency, and technical proficiency in the development/validation of analytical methodology and GMP testing support for your project.