Explore how digital transformation is revolutionizing the life sciences industry. Learn how Compliance Group Inc ensures ...

Explore how a risk-based validation approach enhances regulatory compliance and reduces costs. See how the combination of CG ...

Discover how a risk-based CSA approach combined with paperless validation streamlines compliance, boosts efficiency, and ...

Also meet our experts Caroline Honold and Swati Amanabolu onsite to discuss AI Validation, CSV/CSA, Veeva Vault, Polarion ALM, and the upcoming ISPE Digital Validation Tool (DVT).

Change management is when an organization creates a step-by-step protocol to manage and implement modifications to products and processes. A change management plan is a protocol that implements and ...

So, Quality Management System has produced a step-by-step process to help companies handle the CAPA process to get satisfactory results in adherence to ISO (International Standards Organization) FDA ...

Companies in the life sciences, food, and cosmetics industries are all too aware of how fickle the market is, how dynamic their studies and those under investigation are, as well as their timelines ...

Quality Records and Documents – Non-Conformances (NC), Corrective Actions and Preventive Actions (CAPA), Change Requests (CR), Bill of material (BOM), Complaints, SOPs, Work Instructions, ...

In the life sciences industries, documentation plays a crucial role in proving the product’s effectiveness and safety. Furthermore, it discusses the processes and practice’s dependability, ...

The development of new medical devices or any new project brings a new set of risks. A Risk Management Plan (RMP) must be developed at the start of the Risk Management Process for a new project or ...