Quality Assurance

The following are valuable topics that can benefit professionals, whether they are new to the field or have years of experience. This website is regularly updated, so be sure to revisit and share it with others for optimal results in your professional endeavors.

ALCOA++: Data Integrity to the Next Level

Vendor Development in Pharmaceuticals

GMP Audit Checklist for Pharmaceutical Industry

Transportation Vendor Audit Questionnaire

Pre-audit questionnaires for Raw Material Suppliers

Questions and Answers about GMP in the Pharmaceutical Industry

Vendor Audit Checklist in Pharmaceutical Industry

Initiate Quality Risk Management (QRM) Process

Why are SOP's Important in the Pharmaceutical Industry?

What is Root Cause Analysis (RCA) in Pharmaceuticals?

Audit Checklist for Engineering Department

Audit Checklist for Purified Water System

Audit Checklist for Production Department

Control of Nonconforming Products

Root Cause Analysis (RCA) and Tools in Pharmaceutical

Vendor Audit for Validation

Deviation Management - Pharmaceutical Industry

Difference Between Deviation and Incident in Pharmaceutical

Capsule Failing In-Process Weight Variation Test

Root Cause Analysis in Pharmaceutical Industry

Root Cause Analysis and its Implementation

Checklist for OOS Investigations in Pharmaceutical Industry

Audit Checklist for Quality Control Department

Audit Checklist for Store Department

Failure Investigation and Root Cause Analysis

Out of Specification & Out of Trend Investigations

Factory Acceptance Testing and Site Acceptance Testing

Interview Questions and Answers for Quality Assurance

What are Reworking and Reprocessing?

Roles, Responsibilities and Job Description of QA Manager

Validation of CAPA through Risk Management

Roles and Responsibilities of Quality Assurance Officer

Data Integrity Checklist for Pharmaceutical Industry

What is Data Integrity and Why is it so Important?

Quality Assurance Vs Quality Control

Concept of Electronic Record and Electronic Signature

Frequently Asked Questions (FAQ): Data Integrity

How Long Can We Use API and Excipients after Retest?

User Requirement Specifications in the Pharmaceutical Industry

What is Deviation in Pharmaceutical Industry?

Factory Acceptance Test Protocol

Use of In-house Reference Standards Beyond Pharmacopoeial Standards

Interview Questions and Answers for Quality Assurance

Audit Checklist for Data Integrity

Common cGMP Violations in the Pharmaceutical Industry

Importance of Electronic Records and Signatures in the Pharmaceuticals

Skip Testing in Pharmaceutical Industry: Where to Apply?

Contamination and Cross-Contamination in Pharmaceutical Manufacturing