Compliance Group is proud to be a part of Veeva Summit 2025 as a Silver Partner. Connect in Boston, Sept 2–4, to explore ...

Description: As industries in the Life Sciences undergo digital transformation, moving away from traditional Computer System ...

In this session, Compliance Group (CG) will showcase a Siemens ISV low-code Mendix mobile app enabling Manufacturing and Quality leadership to answer questions they have struggled with for years – ...

In today’s fast-evolving life sciences industry, leveraging Veeva’s cloud-based solutions is critical for maintaining a competitive edge. To drive long-term efficiency, the Veeva Services team ...

Organizations must develop a written method to approve papers for sufficiency prior to issuance. Documents should be reviewed, updated as needed, and re-approved. Determine the changes and the current ...

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 ...

The US Food and Drug Administration (FDA) is responsible for protecting public health by ensuring medical devices’ safety, efficacy, and quality. The agency has developed a rigorous medical device ...

Packaging and sterilization validations are a critical step in the development and manufacturing of medical devices, as they ensure patient safety, regulatory compliance, product quality, and the ...

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