Daily Business Support for GMP Projects 

Seamless integration. Sustained compliance. 

At IVITAA CONSULTANCY, we offer dedicated GMP support by embedding our experienced professionals directly into your workflow—either on-site or online for up to 20 hours per week. This model ensures consistent execution of GMP-critical tasks with the flexibility and precision your operations demand. 

Our DAILY GMP Support covers:

PQR Development & Preparation
Structured creation and review of Product Quality Reviews in line with regulatory timelines.

Stability Report Preparation
Data compilation, analysis, and formatting of stability studies for product lifecycle management.

Complaint Handling & CAPA Coordination
Timely investigation and documentation of market complaints with aligned corrective actions.

Batch Record Review
End-to-end verification of manufacturing documentation for release readiness.

Quality Deficiency & Deviation Reports
Root cause analysis, documentation, and closure tracking of quality incidents.

Release Document Support
Preparation and verification of required documentation for product release.

Change Control Management
Oversight and documentation of change requests, ensuring traceability and risk evaluation.

Regulatory Document Review
Detailed cross-verification of marketing authorization content for alignment with technical data.

Qualification & Validation Assistance
Support for protocol drafting, execution, and documentation in equipment and process validation.

Document Organization
Signature tracking, structured archiving, and compliance-based filing systems.

Other Daily GMP Operations
Execution of any additional GMP-related tasks assigned as part of your operational objectives.

We bring consistent expertise where it matters most—inside your processes, alongside your team.