**Joel Russo – Pharmaceutical Microbiologist, Manufacturing & Lab Compliance Senior Consultant, Russo Consulting Group, LLC**
Joel has 30 years of Microbiology experience including nearly 25 years of experience in pharmaceutical and other areas of GMP Manufacturing Quality, Compliance, and GLP Quality Laboratory Processes and Systems, specialised in Microbiological Control, Aseptic Processing, FDA Remediation, Quality Systems remediation in response to regulatory actions, 483’s Warning Letters, Consent Decrees, other regulatory reporting. Leading, mentoring and supporting investigation / CAPA committees and workgroups. Support of multiple PAI and FDA Product Approval efforts. Joel is currently the President of Russo Consulting Group which specialises in microbiological contamination control, laboratory and lab system architecture, lab compliance, manufacturing compliance, and validation efforts.
**FAQs**
**Is the panel discussion free?**
Yes – there is no charge to watch the panel discussion, either live or on-demand.
**When will the panel discussion take place?**
27 February at 3pm GMT.
**Can I watch it later?**
The panel discussion will become available to watch on-demand shortly after the live webinar takes place.
**What are the benefits of attending live?**
You’ll be able to ask the speakers your questions, which will be answered live in the Q&A towards the end of the session.
**How long will the panel discussion be?**
This panel discussion will last up to an hour.
**What do I need to watch this panel discussion?**
All you need is a computer with an internet connection. We recommend using headphones if possible if you’re in an office environment.