TMQA prides itself on providing flexible, credible and cost-effective services.  We tailor our services to meet our clients' needs and provide support when and where they need it, from short ad hoc projects to long term QA collaborations.  Our principal areas of expertise are:

• Clinical
• Pre-clinical
• Early phase and pre-regulatory
• Academic, NHS and other non-commercial
• Pharmacovigilance

Audit and Inspections
We conduct inspections and audits to verify compliance with GXP or ISO standards

• GCP - Investigator Sites, Database/Data Management, Vendors and Service Providers, Clinical Study Reports
• GLP - Implementation, Facilities, Entire QA Programmes, Study Plans, In-Life Inspections, Reports
• GMP - Manufacturing systems, Interim support, Investigational Medicinal Product management
• Pharmacovigilance - PV systems, safety reporting for trials and licensed products
• Research Systems - Generic Quality Management Systems to support valid research outcomes

Training
We provide a full training service from identification of training needs through bespoke design to effective delivery

• Practical training for those involved with GMP, GCP, GLP and Research Quality Systems
• Personal skills for participating in Regulatory Inspections
• Specialised training for Quality Assurance staff

Consultancy
We can help you to implement practical Quality Systems or review your existing systems

• Comprehensive gap analyses
• Implementation plans
• Vendor and suppier reviews
• Ad hoc or continuing support