System Design, Managements and Documentation

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

We can assist you in the different steps of Cleaning Validation

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

Market Research and Feasibility Study for New Pharmaceutical Manufacturing Facilities

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

cGMP Audits & Gap Assessments