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FDA Form 483 and Warning Letters: What's the difference?

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Data Falsification in Life Sciences: Absolutely Not!

7 Common Phone Interview Mistakes & How to Fix Them

Single-Use Technologies in the Biotech Manufacturing Process

Medical Device Hacking: The Real Risks

Streamlining Data in Pharma & Biotech

Regulation of Mobile Medical Apps

Always Be Networking – 4 Easy Tips to Advance Your Career

Combination Drug-Device Products

Observations from the 24th Annual ISPE Boston Area Chapter Product Show 2015

Root Cause Analysis (RCA)

EG Life Sciences to Exhibit at Boston Area Chapter Of The International Society of Pharmaceutical Engineers ISPE 2015

Targeting the Same Rare Diseases With Different Approaches

Google’s Big Life Sciences Bet

Helpful FDA Material for cGMP Inspections of Biologics Facilities

Customer Complaints: Why They Matter

Life Sciences Clusters

Finding Talent

Mergers and Acquisitions

Remediation - A Delicate Balance

PAI - Pre Approval Inspection

Validation of Electronic Records

A Shifting Landscape of Medical Device Regulation in Europe

How does the FDA ensure Drugs Work and are Safe?

Now is the time to go Electronic

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The Many Faces of Biotech Manufacturing

The Quality Assurance (QA) Unit

Orphan Drugs

The Subject Matter Expert Advantage

Change Controls in the Pharmaceutical and Biotechnology industry

Quality System Backlogs

Post Market Surveillance and the FDA

The Biotechnology industry has experienced explosive growth over the last 10 years

Did you attend Interphex 2015?

Why cGMPS Are So Important!

Do you have the necessary team in place to produce your product to meet FDA regulations?

The importance of a robust CAPA and Deviation System

Taking the Risks out of Responding to FDA Observations

EG Life Sciences New Site

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