Our Services
From pre-clinical research to pharmacovigilance, we can help you ensure regulatory compliance across all of your research activities.
Preclinical Research
Good quality preclinical research forms the foundation upon which potential new treatments and therapies are built.
We provide expert oversight that ensures promising candidates are thoroughly assessed for safety and efficacy before advancing to human trials, minimising the risk of investing time and resources into the clinical development of ineffective or unsafe interventions, improving the likelihood of successful medical advancements.
Our range of services include:
Screening and early-stage research oversight
Study Inspections
Data Inspections
Report Inspections
Facility and System Evaluation
Good Clinical Practice
Good quality clinical research is essential in providing the robust scientific evidence necessary to determine the safety and efficacy of medical interventions, ensuring patients receive treatments that are both effective and safe.
Headway Quality Evolution provides expert oversight of all aspects of the clinical research programme, enabling our clients to make informed decisions leading to better patient outcomes and ultimately, improved public health.
Our range of services include:
Investigator Site Audits
System Audits
Document Audits
Vendor Audits
Trial Master File
Data Management
Regulatory Readiness inspection
Laboratory Audits
Good Pharmacovigilance Practice
Good pharmacovigilance is crucial in the monitoring and assessment of the safety of pharmaceutical products after they enter the market.
Headway Quality Evolution provides expert support in identifying and mitigating potential risks and adverse effects to protect patient well-being.
Our systematic surveillance and analysis of drug safety data contributes to the continuous improvement of our client’s drug therapies and consequently the maintenance of public confidence in healthcare.
Our range of services include:
PV System and Process Audits
Documentation Audits
Third-Party Audits
Computerised System Validation
Computerised System Validation (CSV) supports regulatory compliance and the credibility of research outcomes in the highly regulated fields of drug development and testing.
We can support and provide oversight of computer system validation activities vital for the maintenance, integrity and traceability of data generated during preclinical and clinical studies, ensuring the accuracy and reliability of research findings.
Our range of services include:
GLP/GCP process design consultancy
Documentation Audit