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Quality Assurance

Quality Assurance

Current Good Manufacturing Practices – CGMP in Pharmaceutical Industries

Procedure for Sampling in Process Validation

Writing Effective SOPs in Pharmaceuticals

Possible Causes of Out of Specification

Requirements of FDA for Training in Pharmaceuticals

Tips to Develop Equipment Cleaning Procedure

Gap Analysis for Regulatory Compliance

Cleaning Validation of Manufacturing Equipment

Quality Inspection in Pharmaceuticals

30 Common Ways to Avoid the Most Frequent GMP Errors

Types of Purified Water Systems in Pharmaceuticals

Top 5 Tips for a FDA Inspection

Why Firms Must Avoid FDA 483 and Warning Letters?

What Does Quality Really Mean for Pharmaceuticals?

Quality System in Pharmaceuticals

How to Write a Validation Master Plan?

Importance of Validation in Pharmaceuticals

Cleaning Validation Procedure for Clean-in-Place Systems

Sampling in Cleaning Validation in Pharmaceutical Industry

Recovery Factor Determination in Cleaning Validation

Purpose of Process Validation in Pharmaceuticals

Three Consecutive Batches for Validation in Pharmaceuticals

Validation of Compressed Air

Contamination Control Strategies for Manufacturing Area

Self Inspection and Its Implementation in Pharmaceuticals

Site Acceptance Test (SAT)

Requirements for Good Documentation Practice (GDP)

Preparation of Master Formula Record (MFR)

Preparation of Batch Packaging Record (BPR)

Cleaning Validation of Pharmaceutical Equipment

FDA Warning Letters for Cleaning Validation

Transport Validation for Pharmaceutical Products

Concept of Revalidation in Pharmaceuticals

Criteria to Choose the Correct Swab for Cleaning Validation

HOW-TO-Write-a-validation-Protocol

Sampling and Testing in Exhibit and Process Validation Batches

Quality Management System (QMS)

Investigation of OOS Results in Analytical Testing

Gemba Walks and Its implementation in Pharmaceuticals

How to Submit a DMF (Drug Master File)

Understanding the US FDA Drug Approval Process

How to Review GMP Documents Like a Pro

Change Control in Pharmaceuticals | Process, Documentation, and GMP Compliance Guide

Deviation Control in Pharmaceuticals | Steps, Documentation, and GMP Compliance

Calibration of Hardness Tester

Best Practices for Drafting a Validation Master Plan

Significance of Validation in the Pharmaceutical Industry

Methodology for Cleaning Validation in Automated Clean-in-Place Systems

Approaches to Sampling in Pharmaceutical Cleaning Validation

Determination of Cleaning Recovery Efficiency through Recovery Factor

Ensuring Product Safety and Efficacy through Process Validation

Pharmaceutical Process Validation with Three Consecutive Production Batches

“Ensuring Quality and Compliance: Validation of Compressed Air Used in Pharmaceutical Processes”

Strategies to Prevent Contamination in Pharmaceutical Manufacturing Areas

Self Inspection and Its Implementation in Pharmaceuticals

Site Acceptance Test (SAT)

FDA Warning Letters for Cleaning Validation

Transport Validation for Pharmaceutical Products

Concept of Revalidation in Pharmaceuticals

Best Practices for Swab Selection in Cleaning Validation

Crafting an Effective Validation Protocol: A Step-by-Step Guide

“Comprehensive Guide to Sampling and Testing in Exhibit and Process Validation Batches”

Quality Management System (QMS)

“Manufacturing Excellence: Distinguishing Process and Product Validation”

“Systematic Investigation of Out-of-Specification (OOS) Results in Analytical Testing”

Driving Operational Excellence in Pharma: The Role of Gemba Walks

Top 10 interview questions about Stability studies.

Top 10 interview questions about GLP , GDP & GMP practices.

Top 10 interview questions about OOS and OOT in pharmaceutical industry .

Top 10 Interview questions about Dissolution apparatus.

Top 10 Interview questions about SOR spectroscopy.

Top 10 Interview questions about UV spectroscopy .

Top 10 Interview questions about HPLC columns.

Top 10 interview questions about GC apparatus .

Top 10 interview questions about HPLC apparatus.

What is equipment capacity and how is it calculated in industrial settings?

What types of filling equipment are used for vaccine production?

What are the six steps involved in the sugar-coating process?

What is tablet twinning, and how does it occur during the manufacturing process?

What regulatory guidelines govern the use of pharmaceutical isolators (e.g., FDA, EU GMP)?

How do the different types of tablets influence the choice and execution of quality control tests in the manufacturing of solid dosage forms?”

What are the steps to calibrate and confirm sieve mesh size?

How is blister foil quantity calculated in pharmaceutical packaging?

Classification of GMP Deficiencies

Interview Questions and Answers for Corporate Quality Assurance

Basic Guidelines for Process Validation in Tablet Manufacturing

Understanding and Managing Out of Specifications (OOS) in Pharmaceuticals: Causes, Actions, and Prevention”

Why Data Integrity Matters in Pharmaceuticals ?

IPQA check points during line clearance

What is a Validation Protocol?

Fishbone Diagram in the Pharmaceutical Industry: A Simple Guide

Why Temperature Mapping is Important in Pharmaceutical Storage Areas

“Why-Why Analysis in Pharmaceuticals: A Step-by-Step Guide to Root Cause Problem Solving”

“The Role of CPPs in Ensuring Drug Quality and Safety”

“Why CQAs and CPPs Matter in Pharmaceutical Quality Assurance”

“Why Critical Quality Attributes Matter in Pharmaceutical Tablet Production”

“Critical Quality Attributes in Pharma: Importance, Impact, and Compliance”

Quality by Design (QbD) in Pharmaceuticals: A Strategic Approach to Enhancing Drug Quality and Efficiency”

“Good Automated Manufacturing Practices (GAMP): Ensuring Compliance and Quality in Pharma Automation”

“Critical Steps for Identifying the Worst Case in Cleaning Validation”
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