How CRM Can Help Medical Device Manufacturers With CAPA Procedures

The FDA’s Title 21 CFR 820 Regulatory Requirement means that manufacturers of medical devices that are subject to FDA regulation need to establish and maintain procedures for implementing corrective and preventive action (CAPA) related to device non-conformity. These procedures must provide for control and action to be taken on any distributed or not yet distributed […]

Salesforce Validation Rule Bypass Using a Custom Permission

Salesforce Validation Rules ensure that business processes are adhered to and that data is entered in a consistent format. Validation Rules run when a record is saved. A user is notified of invalid or missing data entry after clicking the Save button. Custom text instructs the user as to what needs to be changed. What […]