Life sciences professionals need to be informed of training requirements. For compliance, records must document that their training is complete. Manual tracking, follow-up and escalation processes are slow and prone to error. Employee training software for pharma and medical device companies resolves these issues by automating all training coordination tasks.
Process changes in life sciences often require document updates and new training. Connecting documentation and training processes keeps employees' procedure training up to date. This prevents the risk of staff performing their jobs based on outdated standard operating procedures (SOPs), work instructions, or other critical documents in pharmaceutical and medical device manufacturing.
Never worry about your current good manufacturing practice (cGMP) training being up to date. With MasterControl's training management software for life sciences, your training data and documents are stored and easily retrieved from one place. You are always ready for audits and inspections in the highly regulated life sciences industry.
The U.S. Food and Drug Administration's (FDA) current good manufacturing practices (cGMP) are in place to ensure that patients have safe and quality products. Employee training is an essential part of cGMP compliance and maintaining quality in life sciences. MasterControl's training management system helps your employees succeed with their FDA cGMP training for pharmaceuticals and medical devices.
