How Can We Help You?

Not all validation is the same. When you partner with ValSource, you partner with leaders in risk management, process validation, and continued verification. We stand with you every step of the way.

ValSource Corporate Contact Information

  • 610.269.2808
  • 918A Horseshoe Pike,
    Downingtown, PA 19335

Resource Center

Conferences & Events

Upcoming Events: Find out where we are presenting.

Conferences & Events

PDA 490 “Going Deeper than Human Error: Finding More Specific Root Causes to Incidents Involving People” Training with Jim Vesper

In this one-day training course with ValSource's own, Jim Vesper, participants will examine regulatory expectations regarding investigations where people are involved in the deviation, models and tools used in the transportation industry. They will also learn how the brain and certain actions can set up a person to make a mistake.

Read Details Register

2022 Annual Environmental Monitoring Training Program – A Practical Approach to Design, Qualification and Implementation of a Robust and Compliant Environmental Monitoring and Trending Program with Paula Peacos

2022 Annual Environmental Monitoring Training Program – A Practical Approach to Design, Qualification and Implementation of a Robust and Compliant Environmental Monitoring and Trending Program with Paula Peacos

Read Details Click to Register

“Are You Ready for Annex 1? Points to Consider When Doing an Annex 1 Self-Assessment” Presentation with Darius Pillsbury & Stephen Langille, Ph D.

Darius Pillsbury (Senior Consultant) and Stephen Langille (Senior Microbiology Consultant) Presentation: Are You Ready for Annex 1? Points to Consider When Doing an Annex 1 Self-Assessment -- A Comprehensive Review of Annex 1 History, Revisions and the Latest Draft to Ensure Readiness for Annex 1 Compliance & Understanding Its Potential Global Regulatory Impact

Read Details Click to Register

Interactive Training Webinar – “Burkholderia Cepacia Complex Organisms The New General Chapter USP <60> Microbiological Examination of Non-Sterile Products Tests for Burkholderia Cepacia Complex & FDA’s Position on Bcc” with Stephen E. Langille, Ph.D.

Stephen Langille, Ph.D. (Senior Microbiology Consultant) Presentation -- Burkholderia cepacia Complex Organisms: The New General Chapter USP <60> Microbiological Examination of Non-Sterile Products Tests for Burkholderia cepacia Complex & FDA’s Position on Bcc.

Read Details Click to Register

Register to attend “Web of Regulatory Affairs Puerto Rico Edition”

Scheduled December 7 at 10 am PRT/9 am EST, James Vesper a member of the VS consulting team, will be presenting "An Example of Using a Risk-Based Approach for Data Integrity." His presentation will discuss: When do you “verify” an action? What does “verify” really mean? How does verify compare to actions like review or check? This presentation looks at what the US, EU, and PIC/S Good Manufacturing Practice regulations say about confirming that an action or activity has taken place using a risk-based approach that supports data integrity.

Read Details Sign Up

Available Now – New In-Person Training Events

Tired of TEAMS? Zoomed-Out? ValSource’s Training Team is here to connect, face-to-face. You’re ready for real interactions, and we are too. Get to know colleagues, discuss important topics, and learn more – together.

Read Details

4th Annual SMi Pharmaceutical Microbiology West Coast (Virtual) Conference with Stephen Langille

Discover novel approaches and best practices for tackling current industry contamination control challenges at the 4th Annual SMi Pharmaceutical Microbiology West Coast (Virtual) Conference.

Read Details Learn & Register

“Effective Root Cause Analysis and CAPA Investigations for the Life Sciences” with James Vesper, PhD, MPH

Ensure compliance when you transform your root cause analysis and corrective and preventive action (CAPA) investigations. Join James Vesper, Director, ValSource Learning Solutions, on a discussion exploring risk-based alternatives when a definitive root cause can’t be determined.

Read Details Sign Up

“Effective Root Cause Investigation for the Life Sciences” with James Vesper, PhD, MPH

Learn ways to conduct better investigations and corrective actions. This workshop examines a defined, logical process that can be applied to investigations that are performed in the drug, biotech, and medical device industries.

Read Details Sign Up

Continued Process Verification – 2021 PDA

Improving, Modernizing, Transforming – Process Validation Gets a (much needed) Upgrade

Read Details Event Registration

Articles & News

Press, updates, and more important information.

Articles & News

Valid Insights

Read the latest in industry breakthroughs.

Valid Insights

We provide swift, agile solutions to support the end objective.