Discover the advantages of electronic batch records (EBRs)
Manufacturing health care products, such as biologics and personalised medicines, requires a delicate balance between speed and safety. To get therapies approved and out to patients faster, your clinical manufacturing efforts must comply with good clinical practice (GCP) guidelines and current good manufacturing practices (cGMPs).
Electronic batch records (EBRs) help you ensure accuracy, safety, and quality, which are essential to clinical manufacturing.
Clinical manufacturing software integrates processes and gives you real-time visibility of all records, clinical trial materials (CTM), quality, etc. throughout all clinical manufacturing activities.
Your clinical manufacturing software needs to include data capture, sharing, and knowledge transfer in real time. It also needs to provide complete visibility into all your manufacturing processes for quick, informed decisions.
In a cloud-based clinical manufacturing system, clinical processes are automated and managed on a single platform. This allows stakeholders to focus more on their core functional areas.
To integrate your clinical manufacturing software, it’s important to partner with the right organisation. Work with your partner to identify your goals, desired configurations, and integration scenario based on your specific infrastructure.
Learn how MasterControl's electronic batch records (EBRs) software helps your clinical manufacturing achieve compliance and remain competitive.
Learn MoreElectronic batch records (EBRs) streamline and speed up batch record processes by reducing the potential for errors.
Eliminate the long review times and extensive corrections on paper batch records. EBRs save time, elevate performance, and improve quality.
Satisfy regulatory demands by ensuring clinical documents and other artifacts are complete and accurate.