Simplifying Global Compliance
Increase Compliance, Reduce Risk with Integrated Digital Solutions – Webinar Recording/ Transcript
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Increase Compliance, Reduce Risk with Integrated Digital Solutions: Create a Connected System and Streamline Your Operations
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Life sciences companies are far behind other industries when it comes to using digital solutions.
While individual SOPs and systems are each valuable alone, when targeted digital tools are integrated they offer you benefits that are exponentially powerful. Early adopters of interconnected technologies designed for the nuances of the pharmaceutical and device industries give you the best opportunity to be first to market.
Your connected technology — the integration of your electronic document management, training management, risk mitigation, risk management, deviation and CAPA management, and audit management systems — will trigger the kinds of checks and balances across systems that increase compliance and reduce risk.
After all, if you don’t know there’s a problem, you can’t address it.
Presentation Takeaways:
- Save time and money by streamlining processes, automating and consolidating tasks
- Build a robust risk management protocol that automates vital actions in other systems
- Optimize your document controls to automatically trigger important updates that might otherwise take weeks to notice
- Implement a learning management system that goes beyond “read and understood” to ensure compliance
- Ensure your audit tools are flexible and powerful enough to capture compliance issues meaningfully, both internally and externally
- Create an integrated document control and training management strategy to take advantage of automation features of technology
- Incorporate business processes into technology to automate tasks and reduce risk of critical tasks being missed
Win that coveted first-to-market spot. When you integrate your digital solutions you’ll streamline operations, improve quality and mitigate risk. First to market is just around the corner.
- Vice President of Quality
- Vice President of Clinical Quality
- Vice President of Clinical Research
- Vice President of Medical Affairs
- Head of Quality
- Head of Clinical Quality
- Head of Clinical Research
- Head of Medical Affairs
- Director of Quality
- Director of Clinical Quality
- Director of Clinical Research
- Director of Medical Affairs
Meet Your Presenter
Patricia Santos-Serrao, RAC, is Director, Product Strategy at MasterControl. She has been with MasterControl for the past eight years. Prior to that, Ms. Santos-Serrao spent six years with QUMAS. She came from the clinical and regulatory side with companies including Schering-Plough and Boehringer Ingelheim. As such, she has experience as both a customer and a solutions provider. MasterControl has over two decades’ experience bringing quality management solutions to life sciences organizations, from large medical device companies to small biotech start-ups. Both FDA and NIH use MasterControl solutions to help ensure and enforce quality.
