Martín L. Molinari Palacios’ Post

Enhance your quality assurance with virtual reality cleanroom training! Increased Awareness: By showing and explaining what can go wrong in the clearnoom, our #Innerspace Simulator increases your personnel’s awareness for everyday work reality. 👉 Increased Quality Assurance: Understanding consequences in the cleanroom leads to behavior adaption and increased quality culture on operator level. Discover how our Simulator can enrich your training initiatives for effective #contaminationcontrol #training #pharma #cleanroom #annex1

🔎 Are you still searching for effective training methods to reduce your risk of contamination? Major #pharma companies use our Virtual Reality Simulator for the visualization and explanation of important cleanroom principles! 👉 Train in a risk-free environment, discover what is invisible to the naked eye, increase awareness and learn from mistakes! This approach simplifies complex concepts, making them more accessible and enhancing your operators' understanding of effective #contaminationcontrol #virtualreality #simulators #pharmaceuticalindustry

Stay tuned #lcms

Collaboration is key at CTMC which means we are always learning from each other. Here we have our scientists in Process Development wrapping up training with manufacturing operators in a PD Demo run for a new TIL process. Excellent teamwork!!! #celltherapy #celltherapymanufacturing #TILtherapy #processdevelopment #endcancer

Experience seamless lab management with automated workflows, real-time data visibility, and enhanced traceability. Reduce errors, minimize wasted time, and unlock the full potential of your lab operations all while safeguarding sample integrity. Learn more: www.lis365.com #laboratory #softwaresolutions #lis365 #lis #medicalsoftware #clinicaldatamanagement

Why do we have our own accredited calibration laboratory? The baseplate to a strong medical device packaging validation is a multi attribute calibration from an ISO-17025 calibration lab. If you are an ISO 13485 medical device manufacturer it's vital to begin your DOE (design of experiment) with a pouch sealer with time, force and temperature control systems that are calibrated through an accredited lab. Derisk your medical device packaging validation with compliant packaging machine calibrations through our ISO-17025 accredited laboratories.

American Cleanroom Systems invited talk at Del Mar Manufacturing Show April 24, 2024. Topic: Cleanrooms for Electronics and Medical Device Manufacturing. How cleanrooms are used to raise manufacturing yield, improve quality, and meet FDA controlled environment requirement. #acs #cleanroom #modularcleanrooms

Streamline Your Training Product Validation with VETNexus! Ensure your training products align with the Standards for RTOs 2015 by partnering with VETNexus for a comprehensive validation process. Why Choose VETNexus? - Expert Credentials: Our team holds the necessary credentials to conduct systematic validation, ensuring your training products meet the required standards. - TAE Expertise: We are uniquely qualified to provide independent validation services for TAE-related training products. - Streamlined Process: We can collaborate with your subject-matter experts to efficiently validate your training products within your five-year validation schedule. Don’t delay! Simplify your validation process with VETNexus today! #RTOcompliance #trainingproductvalidation #TAEvalidation #VETexpertise

Do you use a standard test method to test your medical devices? If yes, have you validated it? If the answer is YES: congratulations, you can stop reading here. If the answer is NO: please watch the video to learn why validating your standard test method is so essential. 👇 Mainly, we can say that it is important to validate your test methods for 2 reasons: 1. ISO 11607-2 asks for it. 2. If you validate your test method, you know how good the test method is, i.e., you are in control of what’s happening & the probability that bad parts indeed get recognized during a test is significantly higher => lower risk & safer medical devices. Reason no. 2 is the important one. Always remember WHY we do quality management: not only to satisfy notified bodies but to bring safe medical devices to market. 𝐏𝐒: If you have not validated your test method yet, check out our new online step-by-step guide where I explain how to do a TMV correctly. Currently, we have TMV-Guides for the following standards test methods available: 📘ASTM F1929-23 (Dye Penetration Test) 📒ASTM F88/88M-23 (Seal Strength Test) 📗ASTM F2096-11 (Bubble Leak Test) 📙ASTM F1886-16 (Visual Inspection) Lay the foundation for safe medical devices & validate your test methods now. 💪 📌 Check out https://lnkd.in/eSJT6itV #medizintechnik #medicaldevices #testmethodvalidation #medtech

It is absolutely crucial for medical manufacturing teams to be familiar with IEC60601 and how this standard impacts the development of medical carts. Recently, our medical cart development team paired up with our partners at MECA to get an in-depth refresh and insights into the next edition. Stay tuned to learn more about how IEC60601 is applied for medical carts! 💡💉 Learn more about IEC 60601 here >> https://lnkd.in/g-TuneXe #IEC60601 #MedicalDevices #medicaldevice #SafetyStandards