Scientific Software Solutions and Validation Services for Process Analytics, Dissolution Testing and Color Control
Solvias provides all the IT services you need to take the full advantage of chemical and pharmaceutical analytics. We provide you with workflow-based software solutions for both the laboratory and production areas, integrating the analytical instruments of your choice. GMP is a very important aspect of our services, and this extends to our software solutions. We also consult and assist you in obtaining compliance for your existing equipment, in particular with regard to 21 CFR Part 11.
Developing a quality analytical solution requires a detailed understanding of the related workflow. Our specialists have extensive industrial experience in the areas of chemical and pharmaceutical analytics and software validation. By combining these areas of expertise, we develop fully GMP compliant software solutions for laboratory analytics, automation, in-process control, and monitoring.
Computer System Validation
Proof of complete validation of software-controlled systems has become a decisive factor in regulatory audits, mainly due to 21 CFR Part 11. Solvias offers training, consulting, planning and implementation for validation. We provide complete validation documentation and also compile the required Standard Operating Procedures. Our know-how and our skilled workforce are the key to your successful completion of IT validation projects.