Pharma Manufacturing and Quality Management
When patients depend on you, you don’t have time for mistakes. Your therapies need to get to market – stat.
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MasterControl Offers
4 Key Advantages for Pharma Companies
Optimized Pharma Production
Error-prone manual processes put you at risk. With the ability to digitally update, review, and maintain batch records, you can minimize production errors and delays and vastly improve manufacturing efficiency and throughput. Discover what enhanced process control and real-time monitoring of pharma production operations can do for you.
Faster Time to Market
Paper-based documentation and processes create bottlenecks that slow down product delivery. MasterControl’s seamlessly integrated pharma quality management and manufacturing solutions reduce the risk of missing tight deadlines or pharma production targets by removing the need for manual management of documentation and eliminating errors and inefficiencies.
Maximized Data Integrity
Missed signatures, incorrect calculations, and illegible entries are inevitable when pharma production records are manually maintained. With MasterControl solutions, you can avoid the issues that create rework, extend cycle times, and negatively impact product delivery and quality. Plus, you can prevent discrepancies that may jeopardize compliance or cause delays.
Enhanced Visibility
Pharma manufacturers need clear visibility into their production processes. Automating your processes with our paperless pharma quality management and manufacturing solutions eliminates data visibility gaps and provides total transparency into statuses, helping you reduce deviations and compliance risks while always keeping your organization audit ready.
Pharma Manufacturing Trends Unveiled
From AI-driven process automation to personalized medicine manufacturing, the pharma industry is evolving rapidly. Explore the transformative trends reshaping pharma manufacturing this year and beyond. This comprehensive guide delves into the latest industry-shifting technologies, pharma production advancements, economic shifts, regulatory changes, and therapeutic innovations. Stay ahead of the curve and position your organization for success in the dynamic, ultra-competitive pharma industry.
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Learn the State of Digital Maturity in Pharma Manufacturing
MasterControl recently conducted a study to learn why so many companies in one of the world’s most innovative industries are still functioning with manual, paper-based processes — and the results are in. Read the report to find out how your competitors are implementing digital manufacturing solutions and gaining an edge in the market. Learn about the impact modern pharma software is having across the industry.
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Pharma Quality and Manufacturing Solutions
Ensuring proper documentation and quality management should be the goal for all pharma manufacturers from day one. You can start product development on compliant footing with MasterControl Development Excellence, part of the fully integrated MasterControl platform.
In the production and distribution of pharmaceuticals, product quality is always the top priority. The industry’s #1 quality management system (QMS), MasterControl Quality Excellence, provides automated document control, change control, training management, audit management, corrective action/preventive action (CAPA) management, and unparalleled process connectivity. By automating version control, audit trails, and signoffs, the Quality Excellence pharma quality management solution optimizes pharma production and eliminates the discrepancies that increase regulatory scrutiny.
Everyone involved in any aspect of pharma production bears the responsibility for ensuring quality consistency. MasterControl Supplier Excellence helps ensure quality alignment throughout your entire ecosystem of suppliers by combining supplier quality management (SQM), approved vendor lists (AVL), and supplier corrective action requests (SCAR) within the same unified platform.
Pharma manufacturers often struggle to connect quality and manufacturing processes, and too many production lines are still reliant on paper. MasterControl Manufacturing Excellence eliminates paper dependency and automates the last mile of the pharma manufacturing production process.
Once a pharmaceutical product is on the market, its performance must continually be monitored. MasterControl Postmarket Excellence helps pharma manufacturers track customer complaints and resolve issues efficiently, making it easier to sustain product quality and safeguard consumer trust throughout the entire lifecycle of your products.
Resources for Pharma Companies
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GxP Lifeline Blog Posts
How to Reduce Human Error on the Pharmaceutical Manufacturing Floor
CAPA’s will be effective when we can eliminate conditions (causes) that make people deviate from the expected outcome. Therefore, CAPA effectiveness should be measured by root cause recurrence and event recurrence.
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7 Key Concepts in the FDA’s Quality System Guidance for Pharma
These seven concepts are critical to understanding the U.S. Food and Drug Administration’s guidance “Quality Systems Approach to the Pharmaceutical Current Good Manufacturing Practice Regulations.”
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Deviation and Change Control in Pharmaceutical Manufacturing
In pharmaceutical manufacturing environments, strict compliance to approved policies and procedures is essential to keep manufacturing operations in a state of control. Uncontrolled changes like deviations can affect the safety and reliability of products, not to mention the regulatory status of products, directly affecting public health and safety. This is what makes change control – and a paperless system – crucial.
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Case Studies
Getting Global Quality Teams on the Same Page
See how a global pharmaceutical compounder has embraced advanced pharma software solutions to streamline employee training, reduce confusion, and deliver personalized medicine to millions of patients, faster.
Fueling Growth Through Digital Transformation
See how connecting batch records and quality processes within an integrated platform has enabled an FDA-registered 503B compounding facility to increase visibility into actionable data, maximize efficiency with automation, and put controls in place to ensure processes remain compliant at every step.
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Speak with one of the expert consultants at MasterControl to know how.
