2022 State of Medical Device True Quality Summit (Free Event)
Important Event Details: Exemplar is sponsoring the Greenlight Guru 2022 [...]
Download Free Slides: Implementing ISO 14971:2019
ISO14971:2019 Webinar. This Webinar was presented December 16, 2021. Did [...]
Join Our Webinar: Effectively Implement ISO 14971:2019 & Maintain Your Risk File
Join internationally esteemed industry experts Audrey Prosser and Rebecca Waterbury as they discuss [...]
Greenlight Guru Partners with Exemplar Compliance
Exemplar Compliance Partnership Announcement Exemplar Compliance, LLC is excited to [...]
Inspection Readiness: 10 Things To Avoid During Your Next Inspection
Inspection Readiness is an important element to any quality [...]
Celebrating 10 Years with 10 Free Webinars
Pharmaceutical and Medical Device Quality Training. Exemplar Compliance is giving [...]
10 Years and Counting!
Exemplar Compliance Celebrates 10 Years Exemplar Compliance, LLC [...]
Supply Chain Management
Understanding Supply Chain Management There is more to Supply [...]
United States-Mexico-Canada Agreement (USMCA)
Preparing For The USMCA On April 24, 2020, the [...]
Company News Update
Exemplar Compliance, LLC announces new CEO PRESS RELEASE Release Date: [...]
U.S. FDA Pre-Approval Inspections (PAI)
If you have worked in this industry for at least a few years you have probably heard the phrase “PAI” thrown about. What is a PAI? Why is it important? And how can I best position my company and our product?
BioPharma & Medical Device Manufacturers Annual Checklist
Quality checklists are a great way to make sure you don’t forget the important things that keep your process and products in compliance. Here is a list of helpful items for Biopharm and Medical Device companies to consider annually. #QualityMatters