Remote audits and inspections are here to stay. But how can pharmaceutical firms prepare for this new reality?

On May 18, three industry experts participated in the Redica Systems virtual panel discussion webinar, “Remote Audits.” Redica Systems Senior GMP Quality Expert Jerry Chapman, Senior GMP Expert Barbara W. Unger, and Pharmatech Associates, Inc. Executive Director of Regulatory Compliance Stephanie Gaulding answered questions about remote audits and inspections based on their expertise and experience.

Their responses were covered in a series of five articles, which are listed below.

If you missed the webinar, you can still access the recording here.

Remote Panel Discussion

Get a Demo

We can show you insights into any of your key suppliers, FDA investigators, inspection trends, and much more.

Request a Demo