How Pharada Supports Your Team

Our experts work alongside internal teams to support:

Technical decisions with regulatory impact

Deviation investigation and root cause analysis

CAPA definition and effectiveness verification

Inspection and audit readiness

Process and workflow optimization

Technical Decision Support

Guidance on complex operational or quality issues where GMP or regulatory implications must be carefully assessed.

Deviation & CAPA Support

Support in investigation, root cause analysis, and development of effective corrective and preventive actions.

Inspection & Audit Readiness

Preparation and operational support to ensure teams are ready for regulatory inspections and audits.

Key Areas of Support

Specialized Technical Support

API Supplier Evaluation & Audit Review

Assessment of API suppliers and audit reports to identify quality risks, compliance gaps, and regulatory concerns before supplier qualification.

Reference Listed Drug (RLD) Sourcing

Support in identifying and sourcing the appropriate Reference Listed Drug (RLD) required for generic drug development.

PDE & Toxicological Assessment Coordination

Coordination of toxicological assessments and Permitted Daily Exposure (PDE) calculations to support contamination control and cleaning validation strategies.

Who This Is For

Pharmaceutical manufacturers

Quality and regulatory teams

Organizations preparing for inspections

Companies addressing compliance or operational challenges

Pharada delivers support through a flexible and responsive engagement model:

1. On-site or remote expert support

2. Short-term targeted technical interventions

3. Integration with existing quality, regulatory, and operational teams

4. Close coordination with leadership and governance structures

Delivery Model

Need expert technical support?

Our specialists can help your team resolve complex operational and compliance challenges.