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Installation Qualification (IQ): Everything About Equipment Qualification

Discover the significance of Installation Qualification (IQ) in the pharmaceutical industry. This process ensures compliance, optimal equipment performance, and effective risk management, playing a pivotal role in the success of pharma organizations.
Pharmacopoeias are essential references that ensure the quality, safety, and efficacy of medicines worldwide. They harmonize drug standards across different regions, ensuring consistent criteria for purity and potency.
Navigating IT change management within the regulated pharmaceutical sector involves a meticulous approach to ensure compliance, data integrity, and system effectiveness. This blog explores steps, key strategies, challenges and best practices to master this complex process.
Cleaning validation is crucial for FDA compliance in pharmaceutical and food industries, ensuring equipment cleanliness to prevent contamination. It involves meticulous planning, execution, and documentation to verify effectiveness and consistency. Failure to comply can lead to compromised product quality, recalls,
Medical device complaints? Don't sweat it! They can actually be a goldmine for improvement. An effective complaint handling system safeguards patients by identifying and addressing potential risks. It also helps improve devices by providing valuable data for future iterations.
Discover the essential guide to navigating notified body inspections for medical devices with our 10 easy steps. Ensure compliance, streamline the process, and achieve success with expert insights and actionable strategies.
Complaint handling is an integral part of medical device companies’ Quality Management System (QMS). It involves receiving, investigating, and resolving customer complaints related to medical device products and services provided by an organization. Such complaints are related to the safety,
The FDA’s Bioresearch Monitoring Program (BIMO) is critical for maintaining the integrity of clinical trials. In this blog, we explore the nuances of BIMO inspections and offer detailed guidance for clinical researchers to navigate these complex evaluations.