You will now be redirected to the GD3 website
Integrated Analytical Solutions, Inc. is a proud member of Genesis Drug Discovery & Development (GD3), a fully integrated CRO providing services to support drug discovery programs of our clients from target discovery through IND filing and managing Phase I-III clinical trials.
Learn more about GD3About
About IAS
IAS was founded in 2004 to support the growing demand for high quality contract analytical services in the San Francisco Bay Area. From the beginning, we set out to provide the highest level of service to our clients, grounded in a culture of scientific curiosity, open communication, and trusted relationships. This philosophy has helped us grow from a team of 2 scientists in an incubator lab to a current staff of 13. Through referrals and word-of-mouth, our clients have grown to include companies and academic labs around the world.
Though our company and client roster have grown, our approach remains the same. We are scientists serving a community we know and care about. We are proud to cultivate loyal customers because of how we do business. Beyond simply delivering excellent R&D services, IAS strives to build lasting relationships with its clients, fellow services providers and scientific consultants.
Always Audit-Ready
We’re on a mission to provide best-in-class GLP bioanalytical and GMP analytical services.
Commitment to Quality starts at the Top
We are dedicated to the continuous improvement of our Quality Management System. Ongoing activities to ensure that we remain current in our approach to quality include:
- Comprehensive training program
- Responsive to deviations and non-conformities
- Scheduled routine internal audits
- Implementation of corrective actions
- Rigorous sample management program
- Validated computer systems and qualified equipment
Quality Agreements and Statements of Work that explicitly define responsibilities and deliverables
QA Oversight of Critical Records including
- Protocols
- Laboratory records
- Reports
Systems to ensure data integrity
- Traceability
- Security
- Archiving
cGMP and GLP Compliance
- Fully compliant with FDA Current Good Manufacturing Practice (cGMP) Regulations 21 CFR Parts 210 and 211
- Fully compliant with FDA Good Laboratory Practice (GLP) Regulations 21 CFR Part 58 and OECD Principles of Good Laboratory Practice
