R0MN D’s Post

The first article detector can ensure the stability and consistency of product quality. By testing the first product at the beginning of the production line, possible problems in the production process can be discovered in time, and corresponding measures can be taken to adjust, thus avoiding the occurrence of batch defects.

[White paper] Implement a 100% quality inspection system. Read the white paper and discover why the vibroacoustic measurements of end-of-line testing offers 100% quality inspection. https://oal.lu/aWY9e

Understanding how to build to the standards in the LABC Warranty Technical Manual means fewer defects, less waste, and faster builds. This three-day course brings your key personnel up to speed on the main areas on site that generate claims (and the costs associated with claims). Learn more or book here: https://bit.ly/3xb0nkp

Stability Testing and Shelf-life Extension Strategies: Ensuring Product Quality #StabilityTesting: Understand the importance of stability testing in ensuring product quality and compliance with regulations. Image: Test tubes… see more

The purpose of the corrective and preventive action subsystem is to collect information, analyze information, identify and investigate product and quality problems, and take appropriate and effective corrective and/or preventive action to prevent their recurrence.

Feeling frustrated with inaccurate pipets? Get peace of mind with Streck’s Pipet Verification Service. Our Pipet Verification Service kits are a convenient and simple way to verify the calibration of laboratory pipets and ensure compliance with federally mandated regulations. Learn more about how our technicians can help verify the accuracy of your pipettes here: bit.ly/3VhG66U

44-Basics-of-Medical-Device-Packaging.pdf AQL's: Acceptable Quality Levels – example of laboratory conclusion of conforming to visual inspection requirements of 3 batches sampled in one site

When it comes to detecting foreign materials in your product, there are various factors that influence how contaminants are found. Olga Pawluczyk, CEO of PPO, shares how background complexity can affect a detection system's performance. Learn more technical factors that can impact detection on our website: https://bit.ly/4cvNfpS

Is it easy for you to find the documentation for your next audit in production? 📑🔍 Is it a challenge to quickly get an overview of which products, goods, and raw materials are affected by production deviations?  📦⚠️ What these questions have in common is the need for traceability. And this is where AROLINK® has a superpower 🦸♂️ Watch the rest of the video and listen to Niels explain how AROLINK®'s superpower can help you with traceability, documentation, troubleshooting, recalls, and audits: https://lnkd.in/duzSHtJU

Q: If the machine is moved from one place to another do we need to revalidate the machine ? Answer: As per CAP accreditation all common checklist Yes, any single movement of the machine, the laboratory is responsible for determining the method performance specifications are not affected by relocation processes. This requirement doesn’t apply to portable equipment used following the manufacturer’s instructions.