Cleaning Validation Seminar for the Pharmaceuticals Industry
Quality
Engineering & Validation
Starts at: 09:00
Duration: 1 Meeting
Language: Hebrew
The seminar will review the regulatory requirements and guidelines of the cleaning validation lifecycle.
In the seminar, we will learn about examples of authorities' observations, how to avoid common mistakes, and practice.
The topics of the seminar:
-Details of the regulatory requirements
-The lifecycle of cleanliness verification
-How to calculate the cleaning limits
-Risk management for worst-case selection
-Validation of the analytical method
-Microbiological considerations in cleaning
-Validation of the cleanliness of biotechnological products
-Examples of comments from regulatory authorities
-How to avoid common mistakes
-Case study practice
Seminar date - 05/05/2025
Seminar Hours - 09:00-17:00
Location: TLV
Registration Fees:
- Early Bird Rate (until May 20, 2025): 1,200 NIS + VAT
- Standard Rate (starting May 21, 2025): 1,500 NIS + VAT
Secure your spot at the discounted rate before the price increases!
About Iris Shamir, M.Sc.
More than 20 years of experience in the pharmaceutical Industry in various Management QA, Compliance and QC roles.Leading sites to successful FDA and other Authorities inspections. Medical Device and combination products experience. Strong leadership and change Management capabilities.Former GMP Inspector at the Pharmaceutical Israeli GMP Inspectorate (ISCP, Israeli Ministry of Health).
Contact Us
Thank you for registering to the course!
We will contact you soon in order to complete the registration procces.
In the meantime, the course details have been emailed to you.
