Building GSDP System

System Design, Managements and Documentation


Data Integrity and Compliance With cGMP

Build a robust data management system comply with expectations of regulatory authorities

Cleaning Validation

We can assist you in the different steps of Cleaning Validation

Group 88 Copy 5

Improving cGMP Compliance Post-Audit

Identifying deficiencies after a regulator’s audit is never pleasant.

Market Research and Feasibility Study

Market Research and Feasibility Study for New Pharmaceutical Manufacturing Facilities


Computer Software Validation

Software Validation to be in Compliance with 21 CFR 11 and Annex 11

Gap Analysis Pre Audit Assessment

cGMP Compliance Audits & Gap Assessments

cGMP Audits & Gap Assessments