FTI Incorporation

Quality control is the backbone of any manufacturing process. In industries where precision and reliability are paramount, such as electronics, aerospace, and pharmaceuticals, certified particles and defect kit preparation play a vital role. In this blog, we will explore the significance of certified particles and   Defect Kit Preparation   and introduce you to FTI Incorporation (www.ftinfsu.com), your trusted partner in achieving and maintaining the highest quality standards. Certified Particles: Precision at Its Finest Certified particles are microscopic standards used for calibration and quality control. They serve as reference materials to ensure that instruments and processes perform with utmost accuracy. Here’s why they are essential: 1. Calibration:  Certified particles allow manufacturers to calibrate instruments, ensuring that measurements are precise and consistent. 2. Quality Assurance:  They are indispensable for quality control, helping manufacturers det...

In the world of pharmaceuticals and healthcare, compliance with industry standards is non-negotiable. When it comes to vial manufacturing, meeting the requirements of USP 1790 is of utmost importance. This blog will delve into the significance of   USP 1790 Compliance   and the role it plays in ensuring defect-free vials. We’ll also introduce you to FTI Incorporation (www.ftinfsu.com), your trusted partner in achieving and maintaining this compliance. USP 1790 Compliance: A Pillar of Pharmaceutical Quality USP 1790, also known as the United States Pharmacopeia Chapter 1790, sets forth rigorous standards for the quality and integrity of pharmaceutical packaging components, including vials. Compliance with these standards is crucial for several reasons: 1. Drug Integrity:  Vials serve as primary containers for various pharmaceutical products. Compliance with USP 1790 ensures that the drug remains uncontaminated, potent, and safe for patient use. 2. Patient Safety:  Non...