Pharma Services for JetX™

Let science do the talking.

Let us help you develop robust methods or we can perform method feasibility studies for JetX™ in a fully GMP compliant environment. Whether you are looking for content uniformity 'speed trials' or comprehensive feasibility studies to compare JetX™ results agains your manual method, our experts have a proven track record of finding the most suitable method for products ranging from tablets to APIs, semi-solids and many more.

 

  • SPEED TRIALS – Let us help you to build your ROI case with tangible cost saving potential
  • FEASIBILITY STUDY – Scientific study to prove that comparable results are achieved
  • EXPERTISE – Our pharmaceutical professionals are experienced in mastering all analytical techniques
  • COMPLIANCE – Everything we do is about compliance. From test execution to documentation.
  • CERTIFIED – Three US FDA-inspected labs with cGMP compliant processes

Speed Trials & Feasbility Studies.

Since 1973, SOTAX has focused on in-vitro dissolution testing; nevertheless, we offer much more than "just" dissolution-related pharma services.

Let Science do the talking.

To establish that comparable results are achieved, the JetX™ extraction is performed and compared against your existing manual method in a feasibility study. Receive a detailed scientific report that lists products, reference standards, equipment, reagents, solutions, HPLC / UPLC method parameters (including system suitability assessment), and presents the results of the feasibility experiments.

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Focus on Extraction.

Extraction parameters are the key focus when transferring from a manual method to JetX™. The fast flow rate in the Xtraction Cell provides a simple and efficient mechanical extraction that can rapidly accomplish tablet disintegration, traditionally achieved through sonication, shaking, stirring, or homogenization.

To fully utilise its potential, one must have a solid understanding of the different sectors that affect results, such as API characteristics, formulation composition, manufacturing process, and biopharmaceutical performance prediction.

Keep your validated analytical U/HPLC method.

JetX™ allows you to keep your analytical procedure exactly the same, eliminating the need for analytical method revalidation. This seamless integration ensures compliance and efficiency without disrupting your existing workflows. Keep what works and improve what can be changed.

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Return on Investment (ROI)? Let us help you!

Return on Investment (ROI) calculations can be difficult. Not with JetX™. Simply send us samples of your product and we'll do a content uniformity 'speed trial' for you. Our experts prepare samples using JetX™ and provide you with the results for comparison with your current manual method.

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Three Labs. One Philosophy.

SOTAX operates three labs in Europe, USA, and India – all based on the same proven quality management system for best-in-class services in a FDA-inspected, GMP certified environment. Whether you are looking for JetX™ speed trials, require assistance in method development or would like to outsource routine testing, our local experts are there for you.

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