Among the many good things automation has enabled, such as improved efficiency across operational areas, better access to data is one of the most important. Data can provide insights that can help in developing focused strategies, be it in improving production, controlling costs or increasing customer success. However, organizations are not necessarily reaping these benefits.…
By Feb 28, 2019, medical device manufacturing companies should have completed their ISO 13485 transition to 2016 to maintain their certification. The transition brings with it several challenges requiring changes in processes and documents, introducing new ones being, and ensuring not to lose the momentum that could risk current certification. Improvements All Around The implementation…
What difference does it make to build and run an Enterprise Quality Management System (EQMS) on Salesforce.com (Force.com) platform? In brief? A lot. You see, as in Genetics, the qualities of the parent platform are bound to reflect on the apps built on it. That is why an EQMS built on Force.com will deliver to…
Unlike the traditional audit approach where employees are instructed to address only questions asked and refrain from volunteering any extraneous details, the new FDA appraisal model relies on collaboration with employees to discover what’s happening inside the organization relative to best practices. The interactions take place between the appraisal team and “doers” who are responsible…
