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| Name | Summary | Price | Quick View | Registration |
|---|---|---|---|---|
| Data Integrity | Eéndaagse training over het implementeren en naleven van Data Integriteit en het belang van Quality Culture. | € 922 ex. VAT | Quick view | |
| Deviation and CAPA Management | Eéndaagse training over deviatiemanagement, root-cause analyse, impactbepaling en CAPA’s | € 922 ex. VAT | Quick view | |
| EudraLex Volume IV - Licenses & Registrations | Training over vergunningen & registraties in Nederland en de EU. | € 922 ex. VAT | Quick view | |
| External Audits & Self-inspections | PCS certificering voor Lead & Support auditors. Voor externe audits (leveranciers en contractnemers), interne en remote audits | € 1.729 ex. VAT | Quick view | |
| GDP voor de QP/RP Refresher | GDP Refresher | € 922 ex. VAT | Quick view | |
| GDP voor het Middenkader | GDP voor het Middenkader | € 1.729 ex. VAT | Quick view | |
| GMP Basics | Basisprincipes en overzicht van Good Manufacturing Practice (GMP) regelgeving | € 922 ex. VAT | Quick view | |
| GMP for Middle Management in the Pharmaceutical Industry | This training provides an overview of key aspects of quality control for middle management level. | € 1.956 ex. VAT | Quick view | |
| GMP Update Seminar 2023 | Seminar over de wijzigingen in de GMP/GDP wet- en regelgeving in 2023 of die in de nabije toekomst verwacht worden | € 899 ex. VAT | Quick view | |
| Good Distribution Practices (GDP) - also for the Responsible Person (classroom) | PCS certificering voor de Responsible Person (RP) en Aangewezen person (Active Pharmaceutical Ingredient). GDP-richtlijnen en Falsified Medicines voor humane geneesmiddelen en actieve grondstoffen (API’s) | € 1.729 ex. VAT | Quick view | |
| Inspection Readiness | Essentiële onderdelen bij de voorbereiding op GMP- en GDP-inspecties van de overheid. | € 922 ex. VAT | Quick view | |
| Quality Management - The Role of the Qualified Person | Quality Management – exploring the role of the Qualified Person | € 3.225 ex. VAT | Quick view | |
| Quality Management in Drug Development | This three-day training provides insight into the regulatory requirements for drug development from both the viewpoint of regulatory authorities as well as inspection bodies. | € 2.280 ex. VAT | Quick view | |
| Quality Management in Manufacturing of Biopharmaceuticals | Three days on manufacturing biopharmaceuticals & quality aspects | € 2.590 ex. VAT | Quick view | |
| Quality Management in Pharma and Biotech | Four modules offering an integrated approach to quality management in pharma and biotech, and in hospitals, to safeguard the quality of their products. | € 8.550 ex. VAT | Quick view | |
| Quality Management in Sterile Manufacturing | Training on sterility assurance challenges in the pharmaceutical industry and hospital pharmacies. Including new Annex 1 and Contamination Control. | € 2.590 ex. VAT | Quick view | |
| Rootcause Analysis | RCA | € 509 ex. VAT | Quick view |
