Track and trace technologies in pharma help protect people from being exposed to counterfeit medicines. Therefore, traceability in pharma product safety regulations is required in industrialized nations and developing countries.
Although track and trace is a requirement for pharmaceutical product quality, it does pose some challenges for IT, quality assurance, and operational departments that need to integrate the technology into their existing infrastructure and keep it up-to-date.
Failing to keep your IT infrastructure and software up-to-date can potentially lead to critical failures such as data loss and external breaches.
Additionally, outdated technologies and software can impact your OEE, resulting in lost time from system downtime and wasted money on repeating deviations.
Fortunately, you can easily overcome those issues by working with your IT department and other key stakeholders to take advantage of improvements through the following processes:
· Security Updates
· Line Optimization
· Product Upgrades
Join this webinar to learn about key issues impacting your track and trace program and discover the steps you need to take to combat them while improving your Overall Equipment Effectiveness (OEE).
Speaker
Head of Market Management bei Mettler-Toledo International, Inc
Marco Pelka
As Head of Market Management at METTLER TOLEDO PCE, Marco’s main tasks are business development and maintaining market knowledge in Europe and America.
With these responsibilities, he stays up-to-date on all related pharmaceutical regulations, market trends, and the ever-evolving software changes to offer his expertise for expansive global track and trace programs.
Working with our global network of sales, service technicians, and distributors, he helps ensure that traceability is integrated into every project, partnering with the customer for the right solutions that fulfill their business needs.
Webinar Partner
METTLER TOLEDO is a leading global manufacturer of precision instruments and a service provider. The company ranks highly in numerous market segments and is considered a global market leader in many areas.
Join Upcoming Events
The Big Restructure- System Risk Assessment & The Benefits in Application
Free Live WebinarThis webinar will give you an understanding of the purpose of performing a System Risk Analysis (SRA) and its benefits over other risk assessment techniques. ...
Things That Can Go Wrong During a Thermal Validation and How to Avoid
Free Live WebinarThis webinar will help you to take a closer look at what can and will go wrong when performing a validation test. You will also learn all the necessary tips and tricks to minimize the risks when conducting thermal validation. ...
Setting up a Risk-Based Audit Program: What to Consider and Why?
Free Live WebinarGain in-depth knowledge of what to consider when setting up an audit program within a GDP or GMP environment, specifically about factoring in risk analysis methodologies. In addition to understanding ‘what’ is important, participants will understand precisely ‘why’ this is important, why we must consider the wider risk element and why reducing its overall impact is critical to its success. ...
Quality Systems in the Digital Era: Are You Ready for the Future?
Free Live WebinarThis webinar will explore how companies can assess their digital quality maturity and how upgrading to a digital, connected system can provide many benefits. We will examine the latest trends in quality management systems (QMS) and document management systems (DMS) and how they can help companies streamline their operations, improve collaboration, and increase efficiency. Additionally, we will discuss the challenges companies may face when transitioning to a digital system, how to overcome them, and practical next steps. ...
How to Effectively Audit Suppliers and Contractors for Initial Qualification
Free Live WebinarLearn the specific auditing requirements for the initial supplier/contractor qualification and the tools and knowledge you need to plan these audits. We will also cover what to look for throughout the process and when reviewing key documents and quality systems requirements such as SOPs, Validations, Change controls, and investigations. ...