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Resource Center

Conferences & Events

Events: Find out where we are presenting.

Conferences & Events

ESTECH 2023 Training Course – Developing Your Roadmap to Annex 1 Compliance — May 10 in St. Paul, Minnesota

Amanda McFarland, Senior Consultant QRM and Microbiology and James Wamsley, Consultant - Microbiology will be presenting this course.

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INTERPHEX 2023 — April 25-27 at the Javits Center in NYC

No matter where you are in the pharmaceutical supply chain, INTERPHEX delivers relevant solutions through curated education sessions, networking and over 500 global suppliers to source quality product and services.

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PDA Contamination Control Strategy (CCS) Workshop — April 6-7 in New Orleans, LA

Join ValSource instructors, Marc Glogovsky, Amanda McFarland, Patrick Mains, and James Wamsley.

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PDA Annual Meeting — April 3-5 in New Orleans, LA

Join Amanda McFarland, ValSource Senior QRM Consultant and PDA co-chair at the 2023 PDA Annual Meeting in New Orleans, LA — April 3-5.

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PDA West Coast Chapter: Cell and Gene Therapy-Panel Discussion — March 23 in Foster City, CA

Whether you are producing biologic drug substance, conducting sterile fill-finish operations, or entering into cell and gene therapy, this meeting will provide the latest information to help your organization have the knowledge and agility needed to meet the needs of the patients we serve.

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ISPE Aseptic Conference — March 6-7 2023 in North Bethesda, MD

Amanda McFarland, Senior QRM Consultant at Valsource is speaking at the 2023 ISPE Aseptic Conference, March 6-7 2023 in North Bethesda, MD.

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2023 PDA Contamination Control Strategies Workshop — March 1 & 2 in Raleigh, NC

Join us for the 2023 PDA Contamination Control Strategies Workshop — March 1 & 2 in Raleigh, NC.

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2023 PDA Annex 1 Workshop — Feb 27 & 28 in Raleigh, NC

You're invited to the 2023 PDA Annex 1 Workshop — Feb 27 & 28 in Raleigh, NC.

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ISPE CaSA 30th Annual Life Sciences Technology Show – Feb 28, 2023 at the Raleigh, NC Convention Center

See you at the ISPE CaSA 30th Annual Life Sciences Technology Show - Feb 28, 2023 at the Raleigh, NC Convention Center!

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2023 Pharmaceutical Conferences — San Diego, CA

Our very own James Vesper, PhD, MPH, Director Learning Solutions discusses "Human Error as a Root Cause" as part of the "Current Hot GMP Topics

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2023 CURT National Conference — San Antonio, TX

This year's theme: “Construction in a VUCA World: Volatility | Uncertainty | Complexity | Ambiguity.

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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.

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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

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“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

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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.

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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.

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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.

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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.

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“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.

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“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.

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Continued Process Verification – 2021 PDA

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

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Valid Insights

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Annex 1 revision experts.

Our consultants are highly-recognized for their Annex 1 knowledge and expertise. We provide a plan forward through Annex 1 updates, today and into the future.