Biotechnology Engineering Process

The biotechnology engineering process, like so many other regulated processes, requires controlled documentation. From SOPs to quality manuals and from quality manuals to specific procedures, documentation must be controlled for the biotechnology engineering process to function correctly.

MasterControl Biotechnology Engineering Process

Besides providing web-based document control, MasterControl GxP process management solutions also help to streamline biotechnology engineering processes from start to finish.

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Common Headaches of Biotechnology Engineering Process for the Biotech Industry

The biotechnology engineering process often requires scale up tasks from one user or one process to another. For instance, deviation or nonconformance information that should be transferred to those in charge of CAPA investigations or change control orders (within the biotechnology engineering process) will often be managed manually (i.e. with paper-based or hybrid systems) and may become lost or defective due to transcription errors during the manual data transfer from one form to another.

The MasterControl Biotechnology Engineering Process Solutions

With the MasterControl GxP process management software solutions however, the biotechnology engineering process is streamlined so that information such as deviation data is controlled electronically and programmed to trigger subsequent CAPA investigations and/or change control tasks, which in turn may trigger training tasks. The MasterControl GxP process management solution also helps to streamline regulatory compliance documentation and related tasks.

For More Information Contact MasterControl

To learn more about software solutions that help streamline the biotechnology engineering process, please feel free to contact a MasterControl representative.