Do you work in drug development, R&D, pharmaceutical quality assurance and quality control or in regulatory affairs? Join the EDQM virtual training programme comprising nine independent modules on the Ph. Eur., reference standards and the CEP Procedure designed to enhance your expertise.

The training modules will focus on chemically defined active substances and medicinal products.

🗓️ Dates: 01-12 December 2025

🌍 Location: Online

🗣️ Working language: English

VISIT THE EVENT PAGE

Register now to attend all or a selection of modules:

Module 1: General methods, general chapters and general monographs - REGISTER NOW

Module 2: Individual monographs – focus on chemically defined active substances and medicinal products containing them – REGISTER NOW

Module 3: Impurity control in the Ph. Eur. – REGISTER NOW

Module 4: Ph. Eur. reference standards – REGISTER NOW

Module 5: Fundamentals of the CEP Procedure - REGISTER NOW

Module 6: Building successful CEP dossiers: new applications – REGISTER NOW

Module 7: Building successful CEP revision applications - REGISTER NOW

Module 8: Control of impurities: CEP approach – REGISTER NOW

Module 9: The EDQM inspection programme – REGISTER NOW

See also:

• European Pharmacopoeia
• Reference Standards
• Certification of suitability (CEP)
• LinkedIn