Centralize maintenance activities, inventory, and compliance.

Automation in the pharmaceutical industry involves using software, equipment, and processes to enable efficient and reliable pharmaceutical production. This includes using equipment and software to automate processes like blending, granulation, and packaging. It also includes automating equipment maintenance tasks. For example, tools like Alldevice can be used to schedule maintenance, create work orders, and automate spare parts management.

Planned preventive maintenance (PPM) is a type of proactive maintenance that involves regular inspections, repairs, and spare part replacements to prevent equipment breakdowns. In the pharmaceutical industry, this includes using a CMMS like Alldevice to plan, schedule, and track maintenance tasks for pharmaceutical equipment. Pharmaceutical companies use PPM to keep production lines operating, maintain drug quality, and ensure compliance with equipment regulations.

Alldevice is the best CMMS for maintenance automation in the pharmaceutical industry. With our user-friendly CMMS, it’s easy to schedule maintenance of medical laboratory equipment, create work orders, and track all your maintenance activities. Alldevice is the preferred choice for laboratory automation in the chemical industry across many EU countries, including Poland, Latvia, Lithuania, and Estonia.

Yes, Alldevice can calculate the overall equipment effectiveness (OEE) of pharmaceutical equipment. OEE is a key metric for measuring equipment performance, availability, and quality. With Alldevice, you can measure pharmaceutical equipment effectiveness, identify areas for improvement, and optimize your manufacturing processes.

Title 21 of the Code of Federal Regulations (CFR) outlines the rules and regulations for the Food and Drug Administration. Pharmaceutical products must comply with CFR guidelines in order to meet quality and safety standards. According to 21 CFR Part 11 guidelines for pharmaceuticals, electronic records must be reliable, authentic, and equivalent to paper records. 21 CFR Parts 210 and 211 set the requirements for the methods, facilities, and controls used in the manufacturing, packing, or holding of pharmaceuticals.