Save My Seat

Date: May 23, 2018
Time: 11 AM - 2 PM EDT (UTC-4)

register here

Get practical insights helping you to create an auditable risk assessment. This three-hour online workshop, taught by a professional risk assessment advisor, teaches you basic Risk Assessment principles and processes. An example of a risk assessment of a new clean room with a filling line will be used, showing how to determine sample point locations.

There will be several opportunities to submit questions directly to the risk assessment advisor regarding your application.

Attend this online workshop to:

- Gain a working knowledge of the FMEA process as it is applied to processes and product
- Identify potential failure modes as they relate to risks to product contamination of sterile products
- Use a systematic approach to document rationale for selection of risk levels

Attendees will receive a Certificate of Training for FMEA Risk Assessment Workshop.

Pricing for Online Workshop:

Global Pharma GMP Advisor

Lisa Lawson

Global Pharma GMP Advisor

Lisa G. Lawson has over 25 years’ experience in supporting large and small pharmaceutical companies in contamination control, including cleaning and disinfection strategies, aseptic manufacturing and use of risk-based approaches to microbiological quality challenges. She spent 16 years working for Amgen in microbial and mammalian cell culture manufacturing support and helped gain commercial FDA and international regulatory approval of the EPO/NESP manufacturing facility in Longmont, CO.