Validation Resources offers both intensive introductory courses and advanced courses in cGxP subject areas. Courses can be delivered both in Ireland and the UK. Popular courses and subjects include validation, Good Manufacturing Practices (GMP), Good Documentation Practices (GDP), medical devices and SOPs.

Course durations are typically 2 - 6hrs and can be delivered on-site or at a venue of your choice.


  • Introduction to Validation
  • This Instructor Led course can be delivered onsite at your manufacturing plant or a location of your choice. It is designed to introduce the subject of validation to Team leaders, QA Inspectors or Engineers that would like to develop their understanding of validation or refresh existing knowledge.
  • €1600
  • 2 - 10 individuals
  • 8 hours
  • Book Now

  • Process Validation Training (Medical Devices)
  • Process Validation is a requirement of the Medical Device Industry. This course will take you through the validation life cycle with particular emphasis on Process Validation. This advanced course reviews regulatory guidance and best practice in Process Validation, Risk Based Validation and FDA databases.

    (Process Validation Training Course, Solo Validation Resources Limited, Waterford City, Ireland. Reg No. 548069)
  • €1600
  • 2-10 individuals
  • 8 hrs
  • Book Now

  • Introduction to GDP
  • For a comprehensive introduction to Good Documentation Practice (GDP) or if you require a refresher, this course is the right solution for your business and is delivered in a practical and energetic approach. 
  • €490
  • 2 - 10 individuals
  • 2 hours
  • Book Now

  • Introduction to Medical Devices
  • An essential course for Engineering Professionals aiming to cross over from more traditional engineering disciplines, to the Medical Device sector. This course will provide you with a comprehensive overview of Medical Device Engineering and practicable know-how to advance your career.
  • €100 per person
  • -
  • 3hrs
  • Book Now

  • Validation for SMEs (Advanced Level)
  • This course will provide Engineers who are responsible for validation in their organisations an advanced understanding of Validation. It is also the perfect refresher course to update existing knowledge.

  • €3500
  • 2 - 10 individuals
  • 6 hours
  • Book Now

  • GMP Training
  •  This course examines the Principles of Good Manufacturing Practices (GMP). It provides a practical and engaging format for Engineers, Supervisors and Managers to get the most out of the training course. The content and delivery can be customised for Medical Device companies or Pharmaceutical companies as required.

    Course Content includes:

    -Review of Regulatory bodies

    -Overview of GMP Requirements

    -GMP Culture and Compliance

    -Current Develops in Legislation and industry

  • €790
  • 2-6 individuals
  • 3hrs
  • Book Now

  • ISO 13485 Medical Device Directive
  • This ISO 13485 training course gives participants a broad understanding of the various requirements outlined in the medical devices standard ISO 13485 requirements
  • €2600
  • 2- 10 individuals
  • 8 hrs
  • Book Now

  • Introduction to Clean-In-Place (CIP) for Pharmaceutical Processing
  • This course reviews the life-cycle and risk based approach to Cleaning Verification and Validation. Typical Cleaning requirements for Pharmaceutical Processes are examined.


    Course content covers:

    Principles of Clean-in-Place

    Principles of Production Line

    Cleaning Design Space

    Risk Based Cleaning Methodologies

    The Life Cycle Approach to CIP

    Cleaning Verification and Cleaning Validation

    Controlling Risks with Production Line Switch and Clean-in-place

    Deficiencies in Cleaning Validation and Internal Auditing Practice’s


  • €1600
  • 2-10
  • 3 hrs
  • Book Now

  • ISO 9001 Quality Management System
  • ISO 9001 is a Quality Management System that is used across various different industries to grow and improve businesses. It fosters continuous improvement and measuring and responding to customer requirements. 

    This course will introduce you to the core principles of ISO 9001 and how to start the implementation process. It contains lots of examples on how to get the best out of ISO 9001.


    Note: Validation Resources Limited also works with companies to take the journey to formal Certification to ISO 9001. We also can offer an Enterprise Software solution provides an integrated Customer Relationship Management (CRM) and Order Processing capability.

    Please contact us for further information.

  • €1,500
  • 2-10
  • 3 hours
  • Book Now

  • Precision Cleaning for Medical Devices
  • This course takes participants through the Validation Lifecycle of a typical Precision Cleaning system*.

    It introduces key terminology and concepts relating to cleaning Verification and Validation and walks through Equipment Qualification, Process Operational Qualification and Performance Qualification.

    *Solvent based system.

     

  • €1600
  • 2-10
  • 3hrs
  • Book Now

 Process Validation Course “I thoroughly enjoyed the course and thought it was well presented”

Karl Walsh, Bsc (Hons) / Waterford City

Process Validation Course -“An insight into the requirements of  medical device manufacturing, practical with real life examples of how to implement the theory discussed.Very professional, I look forward to the next course."

M. Doyle-Kent / Department of Engineering Technology, W.I.T

Process Validation "genuinely interesting and will help me in my future work"

T. Bamboolal / Researcher, University of Leeds