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Predicting Drug Development in 2023
Posted by:
Sandra Acosta
2022 Breakthroughs
Posted by:
Sandra Acosta
The Future of Biotech and Pharma Manufacturing: Part 2
Posted by:
Sandra Acosta
Vendor Audit: What It Is and What to Expect From It
Posted by:
Nagadip Rao
Warp Speed, Vaccines, and Agile Practices
Posted by:
EG Life Sciences
Tactics for Agile in Biopharma Research & Development
Posted by:
EG Life Sciences
Waterfall or Agile: Wrong Question!
Posted by:
Bob Ellis
The Future of Biotech and Pharma Manufacturing
Posted by:
Sandra Acosta
Scrumming Scientific Project Management
Posted by:
EG Life Sciences
Pharmaceutical Innovation and Agility
Posted by:
EG Life Sciences
Behind the Scenes: The Production of Viral Vector Vaccines
Posted by:
Sandra Acosta
What are Viral Vectors and How Do They Work?
Posted by:
Sandra Acosta
Cell Gene Therapy and Viral Vectors: How Can They Be Effective for Compromising Diseases and COVID-19?
Posted by:
Sandra Acosta
Automation for Continuous Compliance in BioPharma and Life Sciences
Posted by:
Jim Damato
Viral Controls and Prevention of Cross-Contamination in the Vaccine Industry
Posted by:
Sandra Acosta
Celebrating Eliassen Group’s Brand Evolution and Expanded Service Offerings
Posted by:
EG Life Sciences
Sources of Cross-Contamination in Vaccine Production
Posted by:
Sandra Acosta
What if Continuous Compliance were possible in the Drug Industry?
Posted by:
Jennifer Mariani
EU IVDR Requirements for Certification
Posted by:
EG Life Sciences
Is Agile the Answer to Big Pharma's Digital Revolution?
Posted by:
Jennifer Mariani
How to Handle Out of Specification (OOS) Results
Posted by:
EG Life Sciences
Net Promoter Scores: What Do the Numbers Really Mean?
Posted by:
EG Life Sciences
FDA Form 483 vs. FDA Warning Letters: What's the Difference?
Posted by:
EG Life Sciences
The FDA is On-Site! Checklist for FDA Site Inspections
Posted by:
EG Life Sciences
The Risks of Insourcing All of Your Programming & Statistical Analysis
Posted by:
Antony Goncalves
Prepping for a Successful FDA Site Inspection: Readiness Team
Posted by:
EG Life Sciences
Preparing to Comply with the EU MDR
Posted by:
Emad Lababidi & Richard Crowe
Focus on Compliance: Scale Your Drug Manufacturing Capacity to Support the Product Lifecycle
Posted by:
Mandy Gervasio
Beyond "Just Fix It!" Application of Root Cause Analysis Methodology in SAS Programming
Posted by:
Nagadip Rao
A Total Error Approach for the Validation of Quantitative Analytical Methods
Posted by:
Anagha Kakade
Attend "Core Components for Contamination Prevention & Control in Biopharma Manufacturing Operations"
Posted by:
Stephen Fochios
Data Visualization: The Epilepsy Story
Posted by:
Surabhi Dutta
Who's leading in biotech in 2017? East Coast vs. West Coast
Posted by:
Stephen Fochios
The Process Validation Life Cycle
Posted by:
Alan Greathouse
How to Handle Out of Specification (OOS) Results
Posted by:
Stephen Fochios
Critical KPIs for a Successful FSP Outsourcing Model
Posted by:
Michael Cox
Dissolution Analyses: Comparison of Profiles Using f2 Analysis Calculation
Posted by:
Anagha Kakade
Preparing for Successful Pre-Approval Inspections (PAI)
Posted by:
Stephen Fochios
An Introduction to the Standard Data Tabulation Model (SDTM)
Posted by:
Anilkumar Jangili
What consultants should look for in a life sciences consulting firm
Posted by:
Dana Tarlow
A Look Back at FDA Approvals in 2016: The Downturn
Posted by:
Alan Greathouse
Become a Life Sciences Quality Assurance Consultant: What are the skills required?
Posted by:
Adam Holmes
Life Sciences Clusters
Posted by:
Stephen Perez
Are you attending PhUSE in Deerfield, IL?
Posted by:
EG Life Sciences
7 Common Phone Interview Mistakes & How to Fix Them
Posted by:
Melody Lam
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