Enabling Pharma 4.0 With CSA Solutions.
We are team of talented Validation and QA Engineers helping pharmaceutical manufacturers embrace new technologies in a compliant and efficient way.
Enabling Implementation of Compliant Digital Solutions to Modern Pharmaceutical Manufacturing Problems
Trusted Computerised Systems Validation Services for the Pharmaceutical Industry
With years of experience, CSA Solutions is dedicated to ensuring that pharmaceutical systems meet regulatory requirements in line with industry best practice. We provide comprehensive computerised system validation (CSV) services, including specification and design creation, verification and validation, and quality assurance testing. Our team is well-versed in CFR 211 Part 11, Siemens PCS7, TIA Portal, Beckhoff TwinCAT, and more, ensuring your systems are compliant and efficient.
- Expertise in Siemens PCS7, TIA Portal, Beckhoff TwinCAT and other OT providers
- CFR 211 Part 11 compliance experts
- Comprehensive audit preparation and gap assessments for your GxP computerised sytems
Ensure your systems are compliant and ready for Pharma 4.0. Contact us today for a consultation.
Our Services
CSA Solutions offers a range of specialized services to ensure your pharmaceutical systems meet all regulatory requirements. Our expertise covers computerised system validation, compliance remediation, and audit readiness.
System Specification & Design Creation
We provide detailed system specifications and designs, ensuring your computerised systems are built to meet industry standards.
Verification & Validation
Our team ensures that your systems are thoroughly verified and validated, maintaining accuracy and compliance throughout.
QA Testing & Documentation
We perform rigorous QA testing and provide complete documentation to guarantee the reliability and compliance of your systems.
Audit Preparation & Gap Assessments
We help you prepare for audits by conducting detailed gap assessments and developing compliance remediation plans.
CFR 211 Part 11 Compliance
Our experts ensure your systems meet CFR 211 Part 11 requirements, covering electronic records and signatures for FDA-regulated environments.
Compliance Remediation Plans
If gaps are identified, we work with you to create and implement effective compliance remediation strategies.
Ready to Ensure Compliance?
Let our experts validate your systems, ensuring full regulatory compliance and operational efficiency.
Contact UsContact
We're here to help! Whether you have a question about our services, want to request a quote, or want to discuss any testing or compliance issues you currently face we're happy to assist you.
CSA Solutions Ltd
Jordan Street Studios, 12 Jordan Street, Liverpool, L1 0BP
Call Us
+44 7429 213 321
Email Us
info@csa-solutions.co.uk