Dewetec Training Centre
Mastering pharmaceutical compliance engineering. Dewetec Training Centre equips its own team and industry professionals with hands-on expertise in validation, QA and regulatory standards.
Internal Excellence
GxP mastery for Dewetec's own engineers. Structured mentoring, hands-on validation projects and certification paths that turn talented staff into compliance engineers.
Learning Tracks
Our training centre welcomes both Dewetec employees and external professionals. Courses cover essential foundations as well as advanced compliance engineering topics.
Corporate Compliance
Build a strong foundation from day one with our Onboarding Training Track. New engineers gain practical knowledge of pharmaceutical compliance, GxP principles, quality systems and validation through real-world examples and exercises. The track supports confident, consistent performance from the start and includes assessment and certification.
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External Specialized
Specialist pathways for external engineers who want to advance in areas such as GxP compliance, validation, data integrity, quality systems, or computerised system validation. Each pathway includes practical learning, expert guidance, assessment, and certification to strengthen your professional credentials.
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Onboarding Training track
A structured learning path that takes new engineers and specialists from day one to confident, compliant contributors in pharma and life sciences. Each stage builds on the last, combining theory with hands-on practice so your new hires arrive on projects ready to add value. The programme covers seven focused modules, followed by testing and certification to confirm each learner’s knowledge and practical readiness.
01 Foundations
The pharmaceutical lifecycle, regulatory landscape, historical background and key terminology.
02 GxP
GMP, GDP and GLP principles, EU GMP and FDA expectations.
03 Quality Systems
Deviations, CAPA, change control and documentation practice.
04 Validation &
Qualification
V-model, URS, IQ/OQ/PQ and risk-based approaches.
05 Data Integrity
ALCOA+, computerised systems and audit trails.
07 Progression
Assessment, certification and a clear path to advanced modules.
06 Practical Applications
Real case studies, protocol writing and exercises.
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Specialisation Modules
Targeted, stand-alone modules for consultants and engineers who want to deepen their knowledge in a specific area of pharmaceutical compliance. Choose the modules that match your next assignment, learn from practitioners and earn a certificate that proves your expertise to clients.
01 Computerised System Validation
GAMP 5, CSA, risk-based testing and supplier assessment.
02 Advanced Data Integrity
ALCOA+ in depth, audit trail review and remediation planning.
03 Process & Cleaning Validation
Lifecycle approach, PPQ, continued process verification and cleaning limits.
04 Audits & Inspection Readiness
Supplier and internal audits, mock inspections and handling findings.
05 Quality Risk Management
ICH Q9(R1), FMEA and risk-based decision making on projects.
06 Freelance Certification
Assessment per module and a recognised certificate to share with clients.
No standard price
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Every client is different, so we don't offer a standard price. We tailor each programme to your organisation, team size, objectives, format, duration and certification needs. Contact us to discuss your requirements, preferred delivery format and learning goals. We will review your needs with you and prepare a quotation for the training package that best fits your team.
Start Your Training Journey
Build the knowledge and confidence you and your team need to succeed in pharmaceutical compliance. Explore our onboarding track, specialist pathways and certification-focused training designed for practical application.