Continuously monitor your cleanroom 24/7
The LMS Express Software allows you to continuously monitor your Cleanroom 24/7. As an excursion occurs, you will be notified immediately to respond to problems as they occur. The software will allow you to integrate as many sensors as you would like. LMS Express is offered as an out of box pre-configured option.
Simple, Easy to Use, Intuitive
The LMS Express Software is designed to be simple and easy to use. The software has built-in maps, graphs, charts and data tables so that you can easily view the data you have collected.
Validate Your System
Lighthouse is able to offer IQ/OQ Validation Services for the LMS Express Software. Otherwise, we can provide you with self-executable IQ/OQ documents which would allow you to validate the documents on your own. Our Validation Documents are designed to meet the stringent requirements of today’s regulations and guidelines.
The LMS Pharma Monitoring System is designed to analyze and display data for all phases of pharmaceutical operations. Its advanced design provides sophisticated automated alarming, notification, viewing, reporting, and auditing capabilities to any pharmaceutical facility.
Simplified installation, configuration, and validation are key features. Designed explicitly for high-reliability and secure facility monitoring, LMS Pharma contains comprehensive security with a redundant data collection system and an intuitive, easy-to-use interface.
Ease of Use
LMS Pharma was designed with an ICON-driven user interface which greatly simplifies the user experience. Color-coded status and unique shaped ICONS enhance the already intuitive user interface.
Data at Your Fingertips
With LMS Pharma software you can easily access data when, where you want 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.
21 CFR Compliance
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.
Project Management with 100% Turnkey Solutions
Lighthouse Worldwide 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 30 years. With a 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.