Overview
Event time zones: 10 am EST, NY / 7 am PDT, California / 4 pm CET, Berlin/ 5 pm (UTC +3), Athens & Tel-Aviv / 7.5 pm IST, New Delhi
In the rapidly evolving landscape of the Life Sciences industry, achieving and maintaining Global Good Manufacturing Practice (GMP) compliance while embracing digitalization has become more essential than ever before.
Maintaining global GMP compliance while embracing digitalization poses a complex challenge. Navigating compliance requirements and adapting to digital transformation can overwhelm professionals. And the pressure to meet standards, minimize risks, and accelerate time-to-market adds to the strain.
In this webinar, we will address these challenges. You will gain insight into the interplay between GMP compliance and digital transformation. Also, you will discover actionable practices to confidently navigate regulations, establishing your organization as a compliance leader.
By participating in this webinar, you will:
-Gain a holistic perspective on how GMP compliance and digitalization shape the future of Life Sciences.
-Acquire actionable insights to enhance your company’s compliance strategies and digital transformation initiatives.
-Discover innovative software solutions that effectively address industry challenges and drive growth.
-Network virtually with like-minded peers, experts, and thought leaders in the Life Sciences sector.
-Position yourself and your organization at the forefront of industry trends and advancements.
Don’t miss out on this exceptional opportunity to explore the synergy between GMP compliance and digitalization while discovering the tools to drive your company’s success in modern Life Sciences. Reserve your spot now and embark on a journey toward excellence.
Speakers
-
Ginny LeeExecutive Director of Global ServicesGinny Lee is the Executive Director of Professional Services at Blue Mountain, and with over 20 years of experience in the life science industry, she possesses a wealth of domain knowledge that makes her an invaluable asset to the company.
As the Executive Director of Professional Services at Blue Mountain, Ginny is responsible for developing strategies and operations to deliver best-in-class services in implementation, project management, and educational services to help our customers achieve GMP compliance and maximize profitability.
Ginny focuses on providing world-class onboarding and ancillary services to our large customer base. She leads the Services Delivery and Customer Success teams, both of which are focused on ensuring our customers are incredibly satisfied. Ginny is also responsible for building, leading, and managing an outstanding team to execute these services.
Ginny has been with Blue Mountain for 8 years. Previously, she worked in roles ranging from Quality Assurance Coordinator to Business Analyst Manager. Ginny brings a wealth of experience from her previous roles in the pharmaceutical industry, at a range of companies such as MPI Research, Merck, Tengion, GlaxoSmithKline, and Amgen. With her diverse background in the industry, she brings a unique perspective and skill set to the Blue Mountain team.
Ginny graduated from Penn State University with a Bachelor of Science degree in Microbiology in 2003. Outside of work, she loves spending time with her husband and two daughters.
-
Jennifer ChangQA Intelligence SpecialistJennifer 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 BMQR. Jennifer employs a practical approach to decrypt intricate regulatory guidance, and assists our customers in navigating a complex and evolving compliance landscape.
Partner
Blue Mountain
Website
https://www.coolblue.com/Blue Mountain is the leading developer of asset management products and services designed exclusively for the Life Sciences industry. For more than 30 years, we have worked with 1,000+ customers ranging from niche firms to the Fortune 500. Blue Mountain has helped hundreds of Pharmaceutical, Biotech, Cell and Gene Therapy, Medical Device, and Contract Manufacturing companies achieve GMP compliance and maximize productivity and profitability. In one seamlessly integrated system, Blue Mountain allows you to coordinate calibration and maintenance management, all while ensuring full GMP compliance. Combining the capabilities of a CMMS, EAM, and CCMS, we offer an enterprise-level system that is best-in-class, secure, and scalable. Backed by a proven legacy and built for GMPs, Blue Mountain Regulatory Asset Manager ® (Blue Mountain RAM) enables companies of every size and stage to put best practices in place, achieve compliance, and drive productivity.
-
Who Should Attend:
- Anyone who deals with system validation and qualification, such as ;
Head of Quality, QualityAssurance Manager, Quality Control Manager, Lab Manager, IT specialist, Facility Manager (Validation Engineer)
- Anyone who deals with system validation and qualification, such as ;
- Skill Level: Novice, Intermediate , Expert
-
Topics:
- Unlocking Synergies: Explore how GMP compliance and digitalization can harmonize to elevate operational efficiency and overall performance.
- Navigating Regulatory Landscapes: Stay ahead with a comprehensive understanding of global GMP compliance requirements. Gain insights into the latest updates and best practices for real life case studies that will help you address data integrity issues and operational bottlenecks that hinder progress.
- Digital Solutions for Modern Challenges: Witness firsthand how cutting-edge software solutions seamlessly integrate for GMP compliance and address common challenges faced by Life Sciences companies.
- Our Innovative Solution: Get an exclusive sneak peek into our industry-leading software designed to simplify and streamline GMP compliance and digitalization.
-
Special event information:
- All participants will get a free certificate of attendance courtesy of our event's partner Blue Mountain
What people are saying
Are You Ready To join us?
Share the Event
Related Events
Thursday
August 8
How to Enhance Shop Floor Efficiency with Digital Batch Record Management
Local Time:
Aug 07 2024 |
Thursday
August 29
Drug Substance Freezing Technologies: How to Improve Your Freeze/Thaw Process and ROI
Local Time:
Aug 28 2024 |
Thursday
September 26
Quality Risk Management (ICH Q9): Advanced Practical Applications
Local Time:
Sep 25 2024 |
Tuesday
October 29
Technological Integrations In Pharma Summit
Local Time:
Oct 28 2024 |
No event found!
FAQ
Please check your spam folder. If the email landed in spam, make sure to add us as a contact, so it doesn’t happen again.
If the email is not in the spam folder, please try using a different email address. Sometimes, company security measures intercept email before they get to your mailbox.
If you get an error when clicking the confirmation link, it has probably something to do with a company internal security measures that change the link.
Please try registering again and opening the email on another device or forwarding the email to your private email.
If everything fails, please register with your private email address.
If you attend the live session you will get a digital certificate of attendance emailed to you within 7-working days.
Yes, our event partners will email you the event recording within several weeks.
