GXP Consulting has introduced an extended regulatory compliance and validation project management service.
The extended portfolio of service means that GXP Consulting can ensure companies have the necessary skills, training and support needed to deliver projects efficiently and effectively - while complying with the regulatory requirements of the MHRA, FDA, EMEA and ICH.
Led by Tom Dine, the regulatory compliance and validation project management team at GXP Consulting provides a service that integrates and understands the requirements of the entire drug-development lifecycle; from pre-clinical studies through to the manufacture and distribution of approved drug products.
The GXP Consulting team has experience of successfully delivering projects to its clients worldwide for the approval and distribution of drug products in a variety of regulatory markets.
Expertise within GXP Consulting covers all areas of Good Practice compliance, incorporating Good Laboratory Practice (GLP), Good Clinical Practice (GCP) and Good Manufacturing Practice (GMP).
