What is the role of the Quality Assurance department in pharmaceuticals? This section ensures that medicines and healthcare products being manufactured in Pharmaceuticals are of the highest quality. They monitor multiple steps to ensure the safety and efficacy of pharmaceutical products.
Let us now discuss everything related to the Quality Assurance department. These articles provide information about the critical role of Quality Assurance in the pharmaceuticals. Quality control, testing procedures, regulatory compliance, and other subjects are covered. Reading these articles will help you understand the significance of Quality Assurance in ensuring that the medicines we use are safe and effective for our health.
- ISO 14644‑1 Overview and Recent Revision
- Top 10 Common Audit Findings in Pharmaceutical Manufacturing
- Why-Why Analysis | 5 Whys with Examples
- Non-Conformance Report (NCR) and Their Handling in Pharmaceuticals
- Procedure for Handling of Deviations (SOP)
- List of Stamps, Colors and Types of Document Copies (Master, Controlled, and Obsolete Copy)
- Technology Transfer Checklist For Sending Plant
- Understanding Temperature Mapping of Storage Areas: Procedure and Guidelines
- A Example of Product Investigation and Root Cause Analysis and its Report Preparation
- Way to Improve Investigation Report in Pharmaceuticals
- List of Potential Areas of Deviations in Pharmaceutical
- Audit Check List for Quality Assurance Pharmaceuticals
- Difference between Humidity and Relative Humidity
- List of Quality Assurance SOPs in Pharmaceuticals
- Role of IPQA during Line Clearance
- Quality Assurance Checklist for BMR Release
- Recall And Complaints Procedure for Pharmaceutical Products
- Pharmaceutical Sampling, types, tools ( Guidelines)
- CAPA Corrective and Preventive Action in Pharmaceutical
- User Requirement Specification (URS) in Pharmaceutical
- Cleaning Method Validation in Pharmaceutical by FDA
- 4 Types Process Validation in Pharmaceutical and Protocol