Webcasts
Webinar Date/Time: Thu, Mar 14, 2024 2:00 PM EDT
Join this webinar and discover how Corium Innovations, a commercial-stage biopharmaceutical company, revolutionized its approach to compliance and maintenance management using Blue Mountain RAM's cutting-edge features. Gain practical strategies for enhancing operational efficiency while navigating the evolving landscape of the Life Sciences industry.
Register Free: https://www.pharmtech.com/pt_w/concept-to-culture
Event Overview:
In the rapidly evolving landscape of the Life Sciences industry, achieving and maintaining GMP compliance while embracing digitalization has become more essential than ever before. Join us for an insightful webinar where we delve into the intricate balance between regulatory compliance and digital transformation, featuring real-world insights from Corium Innovations, a leading commercial-stage biopharmaceutical company.
In the past year, Corium Innovations has utilized Blue Mountain RAM to boost compliance and forge a new culture around maintenance management. Their approach involves fostering a culture of compliance at the technician level, which has significantly enhanced their operational efficiency and regulatory adherence. In this webinar, we explore Corium Innovations' journey, showcasing practical strategies for leveraging Blue Mountain RAM's compliance features to enhance operational efficiency, foster a culture of compliance, and navigate the evolving landscape of the Life Sciences industry.
Key Learning Objectives:
Who Should Attend:
Speakers:
Shane McGrath
Validation Manager
Corium Innovations
Shane McGrath is a highly experienced professional in the Pharmaceutical Industry, with a decade of experience in various roles such as Quality Lab Technician, Metrologist, Quality Engineer, and Validation Engineer. He holds a BS and an MBA with a focus on Managing Technology, both from Grand Valley State University. Currently, he manages the Validation at Corium Innovations, where he is responsible for Equipment, Facilities, Utilities, and Computerized Systems. Shane has led the implementation and validation of multiple enterprise-level validated systems, including the successful deployment of Blue Mountain RAM R4 for his site.
Jennifer Chang
QA Intelligence Specialist
Blue Mountain
Jennifer Chang is a seasoned quality professional with over a decade of experience in pharmaceutical manufacturing, bringing specialized expertise in quality systems, regulatory compliance, software quality assurance, and risk management. Through her role as QA Intelligence Specialist, Jennifer leverages profound industry knowledge to promote ongoing compliance and continuous improvement at Blue Mountain. Jennifer employs a practical approach to decrypt intricate regulatory guidance and assists customers in navigating a complex and evolving compliance landscape.
Ginny Lee
Executive Director of Global Services
Blue Mountain
Ginny Lee, the Executive Director of Global Services at Blue Mountain, possesses over 20 years of experience in the Life Science industry. She is responsible for developing strategies and operations to deliver best-in-class services in implementation, project management, and educational services, focusing on GMP compliance and customer satisfaction. Ginny's diverse background in the pharmaceutical industry, including roles at companies such as MPI Research, Merck, and Amgen, brings a unique perspective and skill set to her leadership at Blue Mountain.
Register Free: https://www.pharmtech.com/pt_w/concept-to-culture