Main Point Systems, Inc. is a custom software development firm located in Santa Monica, California. We specialize in distributed workflow management systems for the health care industry, using state of the art development and management technologies within a robust development process. This process incorporates early and frequent customer involvement to ensure that our software products reflect and address the targeted business domain.
Main Point Systems was originally founded in 1998 as a part of GenSys Software. In 2004, MPS spun out of GenSys as a separate, privately-owned corporate entity. We are located 1 block from the beach in Santa Monica, California.
If you would like to find out more about what we do or inquire about joining our team, don't hesitate to contact us.
Main Point Systems
2434 Main St.
Suite B
Santa Monica, CA 90405
Phone: 310.309.6700
Fax: 310.309.6729
MPS specializes in Java-based enterprise software solutions, incorporating to the extent possible the latest best-of-breed third party infrastructure products to allow us to focus on solving the explicit business needs of our clients. Our current products utilize Spring, Hibernate, Wicket and PostgreSQL.
Main Point Systems uses an Agile development methodology to allow early and frequent software releases and the ability to address new and changing requirements efficiently.
The Main Point approach emphasizes collaboration between all team members in solving client business problems as well as performing software architecture and design. We believe in having our team members contribute in as many aspects of the development process as possible rather than being "pigeon-holed" to a single discipline.
Our flagship product--Pipeline 1.0--is a web-based laboratory workflow management system which allows our client to manage millions of samples annually through their pooling and testing processes. This product manages the entire life-cycle of the received samples, from shipment receipt to customer billing.
Main Point Systems' development process has been created to comply with FDA regulations regarding Current Good Manufacturing Practice (21 CFR Part 820). Our dedicated QA department oversees the process and ensures ongoing compliance issues are addressed and incorporated.