Process Validation with focus on Quality Aspects for the pharmaceutical industry – On-demand
By Maya Gefen, M.Sc
Engineering & Validation
Quality Assurance
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
On-Demand - On-site Training
About Maya Gefen, M.Sc
Maya Gefen is a Quality Projects Manager at Gsap with over 25 years of experience in the pharmaceutical industry. She is a recognized expert in cleaning validation, process validation, and compliance with international regulatory requirements. Maya has successfully managed complex quality projects for leading pharmaceutical and medical device companies, including CTS Industries, Rotem Industries, Dr. Fischer, Trima, BTG, Stratasys, and...
Contact Us
תודה על הרשמתך לקורס
אנו נצור עמך קשר על מנת להשלים את תהליך הרישום
בנתיים שלחנו פרטים למייל שהזנת
Comments
Registration Information
Early Bird Discount: 30 days in advance
Group Rates: Available for 3+ participants
Corporate Training: Custom programs for 8+ participants
Contact: Gstudy@gsap.co.il