Subham Patnaik

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Are You at Risk of Losing Traceability in Your Weighing & Dispensing Process

How Critical is BMR Software for Achieving ALCOA+ Compliance in Drug Manufacturing?

In today’s highly regulated pharmaceutical industry, maintaining ALCOA+ compliance is not just a best practice—it’s a requirement. ALCOA+ principles emphasize data integrity, ensuring that all data is attributable, legible, contemporaneous, original, accurate, and accompanied by supporting evidence. Achieving this level of compliance can be challenging, especially when relying on manual processes. This is where BMR […]
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Are You at Risk of Losing Traceability in Your Weighing & Dispensing Process

Are You at Risk of Losing Traceability in Your Weighing & Dispensing Process?

In pharmaceutical manufacturing, maintaining traceability is essential for compliance, quality control, and safety. Losing track of raw materials during the weighing and dispensing stages can lead to batch failures, costly recalls, and non-compliance with stringent regulatory requirements. Without a reliable Weighing & Dispensing Management System (WDMS), the risk of human error, data gaps, and lack […]
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Can MES Be the Missing Link in Your Pharma Manufacturing Success

Can MES Be the Missing Link in Your Pharma Manufacturing Success?

The Gaps in Traditional Manufacturing Systems  In pharmaceutical manufacturing, relying on traditional systems without a Manufacturing Execution System (MES) often leaves critical gaps that hinder efficiency and compliance. Here’s what happens when you don’t have MES in place:    Increased Risk of Errors: Manual data entry in a traditional system opens the door to mistakes, […]
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How Equipment Qualification Enhances Manufacturing Efficiency

Beyond Validation: How Equipment Qualification Enhances Manufacturing Efficiency

Hidden Risks: How Poor Equipment Management Can Compromise Compliance    Frequent Compliance Issues: Regulatory bodies like the FDA and EMA mandate strict guidelines for equipment used in pharmaceutical manufacturing. However, many plants face compliance issues due to inadequate equipment management.   Operational Downtime and Delays: Unplanned downtime due to equipment failure or non-compliance leads to production […]
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Are You Maximizing Maintenance Efficiency with eLogbooks

Are You Maximizing Maintenance Efficiency with eLogbooks?

In the fast-paced world of pharmaceutical and life sciences manufacturing, ensuring that your maintenance processes are both efficient and accurate is crucial. With the increasing complexity of equipment and regulatory demands, traditional methods of tracking maintenance tasks may no longer suffice. That’s where eLogbooks come in—revolutionizing maintenance management by automating processes and enhancing accuracy. But […]
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Is Inaccuracy in Weighing & Dispensing Costing You More Than You Think

Is Inaccuracy in Weighing & Dispensing Costing You More Than You Think?

In pharmaceutical manufacturing, precision is paramount. The very first step in production—accurate weighing and dispensing—lays the foundation for the entire process. However, even a small error at this stage can lead to significant costs, both financially and in terms of compliance. As a digital transformation and automation company with over 25 years of experience in […]
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Why Modern Pharma Relies on eLogbook Software for More Than Just Record-Keeping

Why Modern Pharma Relies on eLogbook Software for More Than Just Record-Keeping

In today’s fast-paced pharmaceutical industry, the shift from traditional paper logbooks to digital solutions has become more than just a trend—it’s a necessity. As regulatory demands and operational complexities grow, the role of eLogbook software has expanded far beyond simple record-keeping. Modern pharmaceutical companies are increasingly relying on eLogbook software to enhance various aspects of […]
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How Electronic Batch Records Are Evolving Trends Every Pharma Manufacturer Should Know

How Electronic Batch Records Are Evolving: Trends Every Pharma Manufacturer Should Know

In the rapidly changing world of pharmaceutical manufacturing, adopting new technology is essential to stay competitive and meet strict regulatory standards. At our company, we focus on digital transformation and automation solutions specifically designed for the pharma and life sciences industry, with a strong emphasis on electronic batch manufacturing records (eBMR). With over 25 years […]
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Function of EBR System

Electronic Batch Records (EBR) systems, including Process XE®, are more than simply a technological advancement in the Pharma manufacturing industry; they are now a crucial component in guaranteeing compliance, preserving the integrity of the production process, and tackling particular problems. Compliance and sterility Sterility is essential in the life sciences production process. The switch from […]
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