- Aseptic Manufacturing
- USP 797 Compounding Labs
- Medical Device Manufacturers
- Filling Lines
- 503A and 503B Compounding Labs
- Blood Banks
- Tissue Banks
- Animal Health Facilities
With LMS Pharma software, get data when, where and in the format you need it. Whether you are at your desk, or at any computer on your network, you can access all of the data you need.
View your data in multiple formats:
- Real Time Maps
- Real Time/Historical Graphs
- Real Time/Historical Data Tables
- Grid Tables
- Alarm Logs
- Event Logs
- Compliance Reports.
- Batch and Lot Reports
Environmental monitoring of critical operations is required by various GMP regulations and must occur before and during these operations without exception. With (optional) data collection redundancy your data will be automatically recorded to two databases simultaneously. With mirrored databases if the main computer fails, the secondary will automatically take over data collection, thus providing you with uninterrupted data collections and alarming.
With unique user ID, password protection, a secure database, auto logout, and password aging, LMS Pharma software was designed for 21 CFR Part 11 Compliance. Our LMS Pharma Software is designed for GAMP5 compliance also.
Lighthouse World Wide Solutions offers comprehensive Project Management services for our Monitoring Systems projects. Our Project Managers manage monitoring systems projects 100% of the time and we have been perfecting our project delivery for over 25 years. With dedicated Project Manager you can be sure your Monitoring Systems project will be delivered on time and within budget.
In the pharmaceutical and biotechnology industries, validation refers to establishing documented evidence that a process or system, when operated within established parameters, can perform effectively and reproducibly to produce a medical product meeting its predetermined specifications and quality attributes. Lighthouse offers validation management and documentation for the particle counters and online monitoring systems we provide to our customers. We follow established cGAMP guidelines for system validation.