QM documentation – Validation
04/05/2023 | 1004
“Direct GMP Basic/Advanced Training and Guidelines for drafting and completing all EU GMP factory documents and documents at the request of the Management Authority right the first time”
Not only training the basic theory of GMP/GLP/GSP at the pharmaceutical factory project, we always promote and practice with you the specific tasks of each specific employee.
Our consulting team includes GMPc Vietnam and Inotek Pharma Solutions - Top 10 consultants to build EU GMP pharmaceutical factories in India with thorough knowledge of EU GMP standards, long experience in consulting manufacturers EU GMP standard machine. Therefore, we confidently affirm that after participating in GMP/GLP/GSP practice, factory staff will not only master the theory but also have proficient practical skills to ensure that the requirements are met High of pharmaceutical factory EU GMP standard.
The EU GMP factory document consultation package includes the following detailed works:
- Appraisal: Develop VMP original appraisal plan, guide the development of factory machinery appraisal outlines, guide risk assessment of machinery and equipment
- Training: develop training modules according to EU GMP principles. Training services will be according to the specific requirements of the contract
- Building SOP system: Guide to building SOP system of quality management system, manufacturing plant, QC, warehouse... Instructions for operating the quality management system according to the written SOP.
