The Enterey Blog

Do You Dumbo Double Dare Us?

Combination Products: Adapting to a New Mindset

Employee Spotlight

Reframing Human Error

4 Rules to Facility Start-up. Check Out Rule #1

Let It Run: Project Portfolio Management

Disaster Recovery Plan: Ready, Set, Recover

Meet With Enterey's Quality Experts at 2014 PDA/FDA Conference

Enterey Helps in the Fight Against Childhood Cancer

Cloud-Based Solutions for Effective Project Management

Modern Rules of Quality Management

Supply Chain Management: How Globalization is Affecting Your Business

Risk Management. Get Your Head in the Game

Enterey's On Cloud 9. Happy Friday!

2 Reasons Why Life Sciences Should Adopt Lean Six Sigma

5 GREAT Ways to Get Rid of Conflict in Project Management

ENTEREY LIFE SCIENCES CONSULTING WELCOMES BACK A FORMER CONSULTANT

ICH Q8 through Q10 Guidances on Quality Impact CMC

Enterey Launches LTAC's Lean Six Sigma Program for the Life Sciences

The PRO Dilemma: Part 1

Enterey News September 2012

PROACTIVE COMPLIANCE. How Does Your Organization Define it?

Laboratory Management System "LIMS" - Lessons Learned

Utilization Maximization in Biotechnology

A Closer Look at Spend Analysis and Biotechnology

Enterey Consultant Saves Biotech Millions in Two Ways

Top Priorities of a Successful Inspection by Mark Tucker

Process Improvement Award Winner with Global 500 Biotech Company

The Five Critical Areas of Project Management

Agency Inspections Are on the Rise

Behind the Scenes of a Facility Maintenance Shutdown

Why Inspection Management Systems Matter

The Importance of Scheduling Facility Maintenance Shutdowns

4 Rules to Facility Start-up. The Final Rule of Facility Start-up.

4 Rules to Facility Start-up. Looking Deeper Into Rule #3

4 Rules to Facility Start-up. Looking Deeper Into Rule #2

4 Rules to Facility Start-up. Check Out Rule #1

Facebook and the Pharma Industry

Pharma, Social Media and the FDA's Delay

Where Do We Go From Here With Our Process Validation?

What Are the Differences in the New Process Validation Guidances?

Key Points & Concepts: FDA’s New Guidance Docs for Process Validation

3 Simple Steps for Successful Process Validation Gap Analysis

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