Services – eminenceqc

Quality Documents

Documentation is the Heart of Pharma Industry. We prepare Step-by-Step instruction, compiled in the Standard operating procedure to achieve efficiency, Uniformity of Performance and Quality

Equipment's commissioning & Qualification

We perform series of inspections, test and assessment or instrument in reliable performance stage. Equipment's URS, DQ, IQ, OQ, PQ, FAT & RQ.

Risk Assessment

Risk assessment in pharma entails the identification of hazards as well as investigation and assessment of the risk connected to exposure. We asses the all the risk associated during manufacturing of your products with their mitigation plan.

Audit

We performing the third party GMP audits of pharmaceutical medicine, Active pharmaceutical ingredient, Raw material and intermediate.

Training

Training is the foundation that every organization wants to get it strong and effective. Our professional team provide the GMP, GDP, GLP, Data Integrity and other Quality training.

Cleaning Validation

Cleaning validation demonstrate a high degree of Assurance of cleaning process. We perform the overall cleaning validation documentation activity

Facility designing

Building design plays a critical role in any industry. Our technical team help in ensure the best out comes and maintain alignment through out the process for facility design practice.

GAP Analysis

All the existing GAP associated with manufacturing of product in Plant, in documentation and any other regulatory requirement are assessed by our technical team.

Investigation Analysis

Investigation of Non-Conformance are need to be performed accurately and precisely with logical reasoning and evidences evaluated by our technical team.