EBR (Electronic Batch Records) are more cost-effective and capable. Global pharmaceutical companies are confronted with issues related to rising operating costs and stricter regulatory and safety guidelines. Pharma company also deal with a variety of product portfolios, which means that accurate and complete documentation is essential to complying with regulatory regulations and standards.
ProcessXE® provides time-tested and results-oriented EBR solutions that enable paperless production while conforming to regulatory requirements.
Why EBR?
Main reason for choosing Electronic Batch Records is that it speeds up documentation and reports. EBR guarantees that process data is thoroughly recorded, collects real-time data and insights, and provides continuous feedback on mistakes and deviations, among other benefits. ProcessXE®, a leading provider of EBR solutions, can help you go paperless while ensuring thorough, error-free procedures. Our EBR system removes variation, reducing costs and increasing efficiency in your production process.
EBR and Quality Assurance
Everyone in the industrial and pharmaceutical sectors stands by the word quality. A departure from the desired level of quality might be disastrous. MBRs trust on quality control staff to check each step mandated by regulatory agencies with solid focus and unblinking eyes. Such a method is prone to mistakes. Errors are eliminated from electronic batch records by integrating automatic quality checks into their digital structure.
Unique Features of EBRs:
- It breaks down topographical obstacles, allowing teams in different parts of the world to work together.
- Provides a comprehensive audit trail to streamline production processes.
- Creates a log for every action taken and every change made, creating traceable records.
- The system ensures security through authentication, authorization, and backup procedures.
- Automated processes help organizations satisfy regulatory standards such as CGMP, 21 CFR Part 11, and FDA.
Benefits of EBR
Advantages of Electronic Batch Records are visible. They help you save time and effort by eliminating the need for data entry, modification, maintenance, and storage. Paper documentation is a labor-intensive task prone to human mistake. EBRs decrease paperwork and reduce mistakes associated with manual work.
Advantages of Using ProcessXE® EBR
Compliance is a term in the pharmaceutical and other manufacturing sectors. Deviation from compliance rules can result in not just costly penalties, but also the firm being prevented from functioning. It can be time-consuming and difficult to keep track of ever-changing regulatory requirements. The most major benefit of using ProcessXE® EBR management is that it is entirely compliant with the FDA, CGMP, GMP, and CFR. Simply said, ProcessXE® EBR fulfils all current pharmaceutical production regulations in the India and across the world.
Batch manufacturing processes are optimized, and resource and equipment allocation is made simpler and more efficiently planned for improved outcomes. It removes human mistake by making Standard Operating Procedures easier to obtain. It is adaptable enough to meet the particular requirements of manufacturing firms with a wide range of products.
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