What you will learn

Computer System Validation

Document required in CSV

QMS system in Pharmaceutical industry

Risk Assessment

Computer System Assurance


The course of Computer System Validation (CSV) is a structured and systematic approach taken to validate computer systems used in regulated industries. The purpose of CSV is to ensure that these systems consistently produce results that meet their intended purpose and comply with applicable regulations and industry standards. It’s important to note that the specific course of CSV may vary depending on the nature of the computer system, the industry, and the applicable regulations. Validation efforts must be tailored to the unique characteristics of each system and its intended use. Additionally, CSV is an ongoing process, and regulatory requirements may evolve over time, requiring continuous monitoring and compliance updates.

Get Instant Notification of New Courses on our Telegram channel.

Quality Management System (QMS) in pharmaceuticals refers to a comprehensive framework of processes, procedures, and practices implemented by pharmaceutical companies to ensure the consistent production of safe, effective, and high-quality products. QMS is designed to meet regulatory requirements, industry standards, and customer expectations while promoting continuous improvement in all aspects of pharmaceutical manufacturing, testing, and distribution. The implementation of a robust QMS is vital for pharmaceutical companies to maintain product quality, safety, and efficacy. It helps build trust with regulatory authorities, healthcare professionals, and patients, as well as safeguards the company’s reputation in the pharmaceutical industry. Continuous monitoring, evaluation, and improvement of the QMS ensure that the company remains in compliance with changing regulations and industry best practices.




Risk in CSV
Warning letters in CSV
Basics of CSV