You don’t have time for mistakes, and you have to move quickly. Patients are depending on you.
Because the costs of drug development continue to climb, you have to work fast. The pressure is on to develop safe, effective drugs quickly. Mistakes cause delays. With each delay, you’re less likely to recover costs and make a profit.
The solution is a digital quality management system (QMS) that helps accelerate the drug development cycle.
Stay within budget and even reduce drug development costs.
Rapidly produce safe, effective drugs while maintaining high product quality.
Avoid mistakes that slow the drug approval process.
Ensure your pharmaceuticals get to market on time.
Data issues risk your reputation. Just ask one of the many pharma companies that recently made headlines because their data was inaccurate. You don’t want that kind of publicity. Negative press coverage almost guarantees you’ll lose the trust of your customers.
Regulators are focused on quality data, and you should be, too. If you aren’t prioritizing data, you not only risk your reputation, but you jeopardize compliance as well. The U.S. Food and Drug Administration (FDA) has stressed time and again that accurate data is critical to the development and approval of drugs. And yet, one of the top reasons for warning letters in the pharma industry continues to be incomplete/inaccurate data.
A digital QMS isn’t optional. With a digital QMS, meet the FDA’s expectations that your pharma company will focus on quality data throughout the product life cycle – from new drug research through post-market safety monitoring.Learn more about our QMS
Nobody was prepared for a pandemic. When active pharmaceutical ingredients (APIs) were suddenly unavailable, it was hard for the industry to pivot. Changes in the economy forced a few pharma companies to file for bankruptcy while others saw their stock prices soar. The one thing you can count on is that your industry will change. Supply chains get interrupted. Customer needs won’t remain the same. Supply and demand for your products will fluctuate.
Stop struggling with:
Supply chain changes and uncertainty.
Consistency across products.
Long review cycles.
Scaling to meet demand.
To remain competitive in pharma, you have to be agile, and that’s only possible if you adopt the right technology.See our manufacturing solution
MasterControl offers the tools you need to connect quality throughout the full product life cycle – from new drug research to post-market safety monitoring.
"Our streamlined quality process and centralized quality management system (QMS) provides our 1000 users a consistent look and feel that has reduced human errors by an estimated 50%."
Digitize and connect systems. Gain visibility into lines, batches, or lots. Easily find what you need without rifling through paper.
Enforce data limits and automatically reject incorrect entries on batch records.
Track and manage suppliers. Improve accountability, communications, and governance.
Achieve right-first-time production, improve data integrity, and shorten review times.
You need system specifically designed to meet the regulatory requirements in pharma.
Have information readily available to help you make data-driven decisions.
Store digital information in a secure, central location. Remote teams can access it anytime, from anywhere.
improvement in right-first-time metrics
Fagron, a 503B pharmaceutical outsourcing company, implemented MasterControl. They eliminated errors and improved right-first-time metrics while standardizing quality across global sites.
MasterControl solutions are designed to help you develop safe, effective drugs quickly. Finally, be able to scale as needed, and be agile enough to respond to the inevitable changes in your industry and market.
Our cloud-based solution with flexible plans ensures you get all the tools you need to get the job done.
Any Business Size
MasterControl can accommodate small startups, global organizations, and everything in between.
Grows with You
As you grow, you can seamlessly upgrade and meet increased demand.