Ananth K - CodonLIMS Blog

ISO 17025 Inventory Vendors VendorValidation

Vendor Validation in LIMS: Ensuring Quality and Compliance Across the Supply Chain

In today’s regulated laboratory environments, maintaining consistent quality standards goes beyond internal operations—it also depends heavily on the reliability of external vendors. Whether it's sourcing reagents, lab consumables, instruments, or even third-party services, ensuring that your suppliers meet strict quality and compliance standards is essential. That’s where

ISO 17025 Consumables Automotive Component SOP Automobile Testing

Automotive Component Testing with LIMS

What is it?Across automotive supply chain, validating the physical behaviour and performance of automotive components is key to safety of customers and will also improve driving experience. Measuring various parameters like compression, resistance, lamps, pedal se sensors, tension, strength etc. on individual components and sub assemblies in accordance to

AAS Air Quality Air Sampling Carbon Monoxide LIMS Particulate Matter

Air Quality Monitoring with LIMS

Why is it important?Air quality can affect every individual and could manifest in either short term or/and long term illnesses. This topic garners more significance in and around industrial neighbourhoods to monitor particulate matter that is part of air. Because of the health concerns there are effective compliance

Consumable History Expiry Date

Consumable Management System

WhatThis system provides options to track availability, expiration, usage and their respective work performance records in a secure and convenient package. With the help of this information, the management can reach the annual goal with low-cost efficiency and an effective outcome. WhyBy using the Consumable Management System, the management can

GMP Instrument Management Personnel Training

Good Manufacturing Practices (GMP)

What is GMP?Good Manufacturing Practices (GMP) is a system that ensures manufacturing products such as food, cosmetics, and pharmaceutical goods which are consistently produced and controlled according to set quality standards. GMPs examine and cover every aspect of the manufacturing process to guard against any risks that can be

Environment Air Sampling Microbilogical effects Surface Sampling

Environmental Monitoring

What is Environmental Monitoring?Environmental Monitoring is defined as the observation of the presence of harmful factors such as toxins, bacteria, chemicals and other pollutants in a specific location. In other words Environmental monitoring describes the processes and activities that need to take place, to characterize and monitor the quality