Nathan Roman

Nov 14, 2024 | labmanager.com | Nathan Roman

Managing a laboratory involves challenges in maintaining equipment, ensuring quality, and meeting regulatory compliance. Many lab managers are unaware of the full range of services offered by external providers, which can ease their workload and improve operations.

Aug 8, 2024 | ellab.com | Nathan Roman |Victoria Andujar |Zoe Hall |Laura Hatchard

Blog Validation How to Qualify an ... Validation Incubator qualification is a critical process in ensuring that these essential pieces of laboratory equipment are properly installed, operate within specified parameters, and meet both manufacturer and user requirements. This verification process ensures compliance with regulatory standards, protects sample integrity, and maintains accurate experimental conditions.

Jun 26, 2024 | ellab.com | Nathan Roman |Laura Hatchard

The FDA describes data integrity as the completeness, consistency, and accuracy of data through its lifecycle. Data integrity also encompasses the way we capture said data, how it’s transferred and stored, how we back up, archive it or destroy it, and how it’s protected.

May 20, 2024 | labmanager.com | Nathan Roman

Precision and accuracy are both critical in the field of analytical chemistry, especially in techniques like gas chromatography (GC). It is through diligent calibration and quality control (QC) that these factors are maintained, serving as the framework for robust systems that safeguard results and adhere to regulatory standards.

Apr 3, 2023 | labmanager.com | Nathan Roman

In the pharmaceutical and biotech industries, the validation of laboratory instruments and equipment is a crucial part of good manufacturing practices (GMP) and good laboratory practices (GLP). It ensures that equipment functions as intended, delivers precise and consistent results, and meets the defined parameters. Lab managers already know the importance of GMP and GLP requirements and the challenges associated with the validation process.