Product Development

The development of Life Sciences software at Laurus Infosystems is a well defined process that ensures a controlled delivery of your product. As a CMMi Level 3 organisation we have rigorous control systems in place and adhere to all documentation that is required by regulatory bodies like the FDA, EMA and others.

User access control is a very important part of the compliance regulations and essential to comply with guidelines of 21 CFR Part 11, Hazard and Critical Control Points as well as ISO standards.