Would it shock you to find out you can implement a future-ready quality management software system in only 30 days and with a limited budget?
This free webinar will show you how.
Most manufacturers of drugs, biologics and medical devices find the push-pull between the advantages of automating — including comprehensive document control management and automated/integrated training management — versus the considerable input of time, money and aggravation to be a difficult choice.
Mickey Landkof, general manager and global vice president of sales for Dot Compliance, will share how to choose the right QMS software system for your company and use industry best practices to get it up and running in 30 days.
He’ll share how some life science companies are approaching digital transformations differently: by taking a holistic approach that hyper-scales the power of data and analytics, for a future-ready QMS.
Mr. Landkof will also explain … how cloud-based technology helps keep IT costs down while maintaining the highest levels of data security … why pre-validated quality software can help you minimize the costs and headaches often associated with implementation … and that you can get useful features including electronic forms, binders and batch records — even on a budget.
Webinar Takeaways:
- Why it takes so long for traditional QMS solutions to go live
- The steps required for a 30-day QMS implementation
- How to save time, money and resources, and decrease time to market by doing away with fully customized QMS solutions — all while remaining compliant with industry regulations and standards
- How to build a future-ready strategy
You can implement a QMS in a fraction of the time — and at a fraction of the cost — without sacrificing the features or functions that drive compliance and regulatory adherence. Start with this free webinar. Join us by registering today.
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Who Will Benefit
Managers, directors and vice presidents of:
- Quality management
- Quality assurance
- Regulatory affairs
- IT
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