Consultancy Services
Our CIP Validation Specialists are experts in cleaning design, with a deep mastery of risk-based validation approaches. They excel in all aspects of the validation process, including URS, DER, DQ, FAT, SAT, IQ, OQ, OV, CV, evaluation reports, traceability matrices, and process-related validation packages such as PC, PfV, and PV. Additionally, they are proficient in designing equipment to ensure optimal cleaning performance.
Our Operations Consultants are experts in deviation handling, problem-solving, managing change requests, conducting risk assessments, implementing logbooks, writing SOPs, and maintaining cleaning monitoring programs.
Our Cleaning QA specializes in regulatory cleaning requirement in the pharmaceutical industry and provides high level of compliance within cleaning validation and operation.
Enhance you documentation package to follow the lates GMP and GDP guidelines. Our consultant will assess existing documentation, identify areas for improvement and implement best practices to elevate the quality and consistency of all records. we can deliver clear, accurate and compliant documentation.
