Process Validation with focus on Quality Aspects for the pharmaceutical industry
Starts at: 09:00
Duration: 1 day Seminar
Language: Hebrew
This course offers an in-depth overview of process validation in the pharmaceutical industry, following FDA and EMA regulations. It covers key regulatory terminology, validation approaches, Quality by Design (QbD) principles, investigation methodologies, and continuous process verification. Designed for professionals in QA, regulatory affairs, manufacturing, and development, it equips participants with essential validation knowledge for compliance and efficiency
Date and hours:
26/5/2025
09:00-17:00
Haifa Matam
Price: 1,200 NIS + VAT
15% early registration discount until 15.05.25
About Maya Gefen
QA manager to work with vast experience working with industry standards and compliance with regulatory requirements.Proven experience in creating procedures and workflows as well as improving existing processes.Management Cleaning validation field; Process Validation field, including regulatory issues for new preparations and manage changes to existing products (by Change control system).Dealing with suppliers of raw materials and packaging materials.Approving process validation...
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