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Get help quickly for any GxP regulatory issue
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Optimize your quality system with our eqms solution
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Taking care of your third party audit requirements worldwide
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(Contract) manufacturers, importers and MIA or MAH holders
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Distributors, wholesalers and WDL holders
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Popular solutions
EU GMP certification
Achieve GMP certification/a MIA faster
GMP for medicinal cannabis
EU GMP compliant medicinal cannabis products
In-house training
In-company training for pharma & biotech
QMS Software
GMP document management software solutions
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Training
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Seminars / Hotel Courses
Discover our offer of seminars, open registration courses.
In-house training
In-company training for large groups and optimal interactivity.
eLearning
Short and interactive eLearning courses for pharma
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Quality Course Modules
Quality Management in Pharma and Biotech
Four modules offering an integrated approach to qua...
Quality Management - The role of the Qualified Person
Quality Management - exploring the role of the Qua...
Quality Management in Drug Development
Three days of training. Date: 20-22 September 2022...
Quality Management in Sterile Manufacturing
Three days of training on sterility assurance chal...
Quality Management in Manufacturing of Biopharmaceuticals
Three days on manufacturing biopharmaceuticals & q...
Featured courses
Quality Management in Pharma and Biotech
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Pharma Training
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Quality Management - The role of the Qualified Person
,
Pharma Training
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Review van Batchdocumentatie
,
Pharma Training
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Customers
About us
Department Contacts
PCS Academy (training)
+31(0)182503280courses@pcs-nl.com
PCS Canada
blake.bissonnette@pcs-nl.com
Sales
+31(0)182503280sales@pcs-nl.com
Finance
+31(0)182503280invoices@pcs-nl.com
Information
About us
Our team, philosophy and mission
Team
Meet our team of consultants & trainers
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Frequently Asked Questions about GMP & GDP
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Resources
GxP Guidelines
A handy tool to find industry & regulatory guidelines
Popular Posts
Responding to Inspection Observations
QP Training Module 1 - Information
The Importance of Uniform Audit Terminology
Contamination Control
GMP OOS - the OOS Procedure
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