itsoli specializes in the unique systems and applications used in the Life Science industry
Our consultants understand the complexities of the lab environment and work closely with your team to implement, manage, and support systems that will meet your pharmaceutical development and manufacturing organization’s goals.
Whether it’s scaling an FDA-regulated application into the cloud, supporting growing biotech’s scale to commercialization, or implementing a data integrity program to support drug development, itsoli has the expertise and experience to support your initiative.
itsoli provides a variety of services in these critical LIS business areas
Quality Management Systems
Regulatory Information Management Systems (RIMs)
Quality & Validation
- GxP Practices
- Computer Systems Validation
- Document Control
Ensure regulatory compliance with a documented audit trail.
Facilitate proper data access and connectivity between disparate LIS systems.
Provide consistent PM planning, delivery, and governance among the uncertainties of scientific research and development.
Support advanced GxP strategies for gathering, reviewing, and analyzing business and technical requirements.
Provide monitoring, management, and remediation of pharmaceutical development and manufacturing systems.
Benefits of partnering
with itsoli in Life
Life Science focused PM methodologies and processes provide confidence that projects will be run efficiently and compliantly to fast track the development and manufacturing of your product offering.
From automating ineffective workflows to meeting regulatory guidelines, itsoli partners with you to implement and manage the infrastructure that supports your compliance standards and facilitates the product development lifecycle.
Our deep understanding enables us to identify the right resources and strategies to support and migrate from legacy systems to taking full advantage of cloud-based technologies.