Pharmaceutical Commissioning, Qualification And Validation Services
Our industry-leading compliance subject matter experts combine their technical and operational expertise in the areas of design, construction, commissioning, qualification, and validation to produce fully operational and compliant commercial operations.
By working on technically complex projects that span across geographic regions, industry sectors, and facility types, we have built an unmatched global regulatory understanding that allows us to provide our clients with effective and efficient regulatory decision making.
Commissioning, Qualification & Validation Specialties
Capital Projects and Existing Facilities
As a full service company, we simply understand and deliver projects extremely well from start to finish. We also support many clients with continuous improvement and ongoing qualification and validation activities in their new or existing facilities.
CGMP Audits
As a global service provider, our compliance experts understand the increasingly rigorous global CGMP regulations and help our clients with conforming to regulatory expectations and requirements.
Commissioning
Our team of commissioning experts possess the experience and technical knowledge to execute the most complex, demanding projects and deliver a value-driven project.
Core C&Q Services
The core of our compliance services is in the support of vendor FATs/SATs and the preparation, execution, and report generation of IQ/OQ/PQ protocols.
CQV Program Development
We apply industry best practices to help our clients develop and implement lean efficient, effective, and fully compliant CQV programs.
Design Reviews and Risk Assessments
IPS has the expertise and tools to support a robust design review and/or risk assessment process.
Quality Management Systems
IPS has a team of experienced quality professionals to support quality system audits and policy and procedure development.
Validation and Data Integrity Services
IPS has industry-recognized SMEs and dedicated teams that support process validation, cleaning validation, computer system validation (CSV) and data integrity, analytical methods validation, and environmental monitoring.