Pharsh Pharma has a culture founded on Quality Management embedded across all our activities. Our Quality Management System facilitates a harmonized approach to the delivery and maintenance of quality and compliance which includes all the aspects in the following diagram:

We work with you on your projects to comply with the Guideline for ICH Good Clinical Practice (GCP) and local regulatory requirements to protect participants and ensure data integrity. We implement our quality management approach through all phases of the project from first contact with the client through study closure and reporting.

We provide global coverage of Clinical Research Compliance and Training, and Quality Assurance with people in the US, Canada and Sub-Saharan Africa.

Pharsh Pharma conducts and maintains:

• A risk management approach to conducting projects and activities
• Audits- for example, investigator site, database, systems, vendors (e.g. GMP, GLP)
• Inspection readiness
• Training and knowledge management
• Comprehensive standard operating procedures
• Process reviews
• Monitoring oversight (quality visits, document reviews)
• Vendor selection, management, and oversight
• Regulatory support