Audit

US FDA Inspection and SMEs Role

US FDA Inspection and SMEs Role

Before Inspection During Inspection Key Phrases Best Practices Common FDA Inspection Questions After Inspection Additional Tips By following these guidelines, SMEs can effectively communicate with US FDA inspectors. Read also: Resource Person: Rajesh Jain
Internal Audit Process in the Pharma Industry

Internal Audit Process in the Pharma Industry

In the ever-evolving landscape of the pharmaceutical industry, the role of Quality Assurance departments has never been more critical. As professionals committed to ensuring the highest standards of product quality and patient safety, we often find ourselves at the heart of rigorous internal audit processes. But what makes these audits ... Read More
Audits and Inspections in Pharmaceutical Industries | Similarities and Differences

Audits and Inspections in Pharmaceutical Industries | Similarities and Differences

Audit: ensure quality and compliance with systematic, independent examination and documented process Inspection: determination of conformity to specified requirements “Audit” can be seen as an umbrella term, whereas “inspection” is one concrete type of audit. Similarities 1) Both involve a review of processes, procedures, and records.2) Both aim to determine ... Read More
Vendor Audit in Pharmaceutical Industry

Vendor Audit in Pharmaceutical Industry

Vendor audit is an evaluation of a vendor manufacturing process, practices, documentations and quality compliance by offline (physical) or online (desktop). Conducting a vendor audit in the pharmaceutical industry is an essential process to ensure that suppliers and vendors meet the required standards and regulations. Vendor Audit Process Define Audit ... Read More