Pharmaceutical (drug) and biotechnology

High-quality process equipment

The production methods in the pharmaceutical (drug) and biotechnology industries set the highest requirements that process systems and equipment must meet. The cGMP guidelines and FDA requirements serve as the foundation for very high-quality process equipment. We will deliver a reliable system that is fully documented. Regardless of whether a large or small project is involved. Smink can take charge of the full process from feasibility up to the system’s PQ. Our 25 years of experience attest to this. And this is where you will also find our added value in the pharmaceutical industry. Our engineers will take a constructive approach with our customers and will draw up the specification documents, after which we will start execution to meet the required deadline and quality.


Meeting legal requirements

The important IQ, OQ and PQ protocols check whether the delivered system meets legal requirements. IQ (Installation Qualification) checks whether the system has been produced in accordance with the blueprints. Once the equipment has been installed, OQ (Operational Qualification) will confirm the operational processes of the equipment. The PQ (Performance Qualification) check must ensure that the equipment is fit-for-purpose for the job for which it was purchased. Smink is ISO 9001 (quality standard) certified and VCA** (SCC) certified (safety standard).