June 6, 2013Sterility Failures Within the Pharma Sector

June 12, 2013FDA Audit for Cleaning Process

June 4, 2013Regulated Requirements Management

May 23, 2013Validation Script Errors and Deviations

May 25, 2013Paperless Validation Testing

May 29, 2013Validation Project Deviations

Validation Project Deviations

May 15, 2013Top Tips for Computer System Validation Protocol Execution

May 8, 2013Access Level Testing – 21 CFR Part 11

April 30, 2013FDA compliant computerized system

April 16, 2013Current Good Manufacturing Practices Discussion Forum

April 9, 2013Purified Water Validation Requirements

April 2, 2013The Problems with Risk Assessments

April 3, 2013Reduce Your Validation Costs With Paperless Validation

March 26, 2013Operational Qualifications Mistakes to Avoid

March 13, 2013Yokogawa Chart Recorder Questions

March 18, 2013Validation Book Sale

March 4, 2013The Pharma Tech Trends for 2013

February 13, 2013Thermocouples in Manufacturing Loads

February 19, 2013GAMP 5 Helping to Reduce Validation Costs

February 28, 2013User Requirement Specification for an Autoclave

February 6, 2013Validation Deviations

January 30, 2013Validation Training Checklist

January 17, 2013Master Validation Plans

January 23, 2013Categories for Software Solutions

January 7, 2013Qualification of Equipment

December 4, 2012Supplier Qualification – Top Tips

December 11, 2012US FDA’s Guide to Process Validation

November 28, 2012Computer System Revalidation

November 6, 2012Validation of Air Handling Systems

November 20, 2012Tablet Assay Method

October 24, 2012Managing Regulatory Requirements for Validation

October 31, 2012Audit reporting for software vendors

October 16, 2012Top Tips for Protocol Development

October 9, 2012Contract Manufacturing – Top Tips

October 3, 2012Equipment Qualification Tips

September 25, 2012Challenges in Production Planning and Control

September 17, 2012The Benefits of Validation Templates

September 5, 2012Regulated Alarm Management

September 11, 2012Validating Purified Water Systems – All You Need to Know!

August 28, 2012GAMP 5 Categories

August 15, 2012All You Need To Know About the Regulated Cloud

August 21, 2012Pharmaceutical Quality by Design

August 6, 2012Validation Test Scripts – Time Consuming Tasks

July 10, 2012Engineering with an S88 Approach (Part 2)

July 24, 2012Efficient Software Testing for a Regulated Environment

July 16, 2012Engineering with an S88 Approach (Part 3)

July 3, 2012Top Tips for Cleaning Method Development

June 26, 2012Electronic Records – CSV FDA Warning Letters

June 19, 2012Quality Improvement in Pharmaceutical Manufacturing

June 12, 2012Annex 11

June 5, 2012Challenges in Pharmaceutical Product Life Cycle Management

May 29, 2012CSV Periodic Review

May 22, 2012Cleaning Validation Template

May 15, 2012HVAC Qualification

May 9, 2012Lean Manufacturing

May 2, 2012MS Access Validation – Top Tips

April 25, 2012Spreadsheet or Excel Validation, There is No Risk!

April 18, 2012Levels Of Flexibilities In Flexible Manufacturing Systems

April 11, 2012Outsourcing Challenges and Strategies For Pharmaceutical Manufacturers

April 4, 2012Manufacturing Engineering Systems And The Challenges

March 28, 2012Vendor Audit

March 21, 201221 CFR Part 11

March 13, 2012Vendor Qualification

March 8, 2012Regulated Environment

February 29, 2012The Difference Between a FAT and a SAT

February 22, 2012Constituents And Factors Of Technology Transfer In Pharmaceutical Industry

February 15, 2012An Easy to Understand Guide to Equipment Qualification

February 7, 2012Software Master Validation Plan

February 1, 2012COTS Software – 5 Essential Items to Consider

January 10, 2012A Paperless Manufacturing Environment in 60 Days!

January 25, 2012The A to Z’s of Microbial Control, Monitoring and Validation of Water Systems

January 19, 2012Top Tips for Protocol Execution

January 10, 2012A Paperless Manufacturing Environment in 60 Days!