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PSI was founded in 2013 in San Juan, Puerto Rico by a Pharmaceutical Industry Team with average 18 years of experience in the industry. The group was formed to design software that was specific for FDA Regulations Compliance in different areas such as management of quality, training, investigations and laboratory management.
We deliver the complete project cycle from design to final implementation. We can perform: Needs Analysis, Process Development, Software Engineering and Project Management. We can also assist in the validation and certification process of the software.
PSI Software product is a cloud based compliance and integrated software service that includes:
· Enterprise Resource Systems
· Manufacturing Execution Systems
· Electronic Batch Records
· Laboratory Information Management Systems
· Document Management System
· Quality Management System
· Learning Management System