Quality Assurance Support
Quality Assurance (QA) support helps organisations maintain effective oversight of regulated activities, strengthen quality systems and demonstrate compliance throughout the product lifecycle.
Tower Mains provides flexible, practical and proportionate QA support to pharmaceutical, biotechnology, healthcare, medical device and research organisations. Our experienced QA professionals provide risk-based support to help organisations maintain compliance, strengthen quality systems, support inspection readiness and embed quality into day-to-day operations.
Whether you require targeted QA expertise, additional resource or an ongoing quality partnership, we provide tailored support aligned with your organisation’s regulatory requirements and operational objectives.
The role of Quality Assurance
Quality Assurance provides independent oversight of regulated activities, helping organisations identify risks, maintain effective quality systems and demonstrate compliance with applicable requirements.
Effective QA helps organisations:
Maintain effective governance and quality oversight.
Strengthen GxP compliance across regulated activities.
Improve inspection readiness and regulatory confidence.
Support consistent, risk-based decision-making.
Embed quality into everyday operations.
Tower Mains provides practical QA support that helps organisations strengthen compliance while building sustainable quality practices that support long-term operational effectiveness.
QA support across regulated environments
Tower Mains provides QA support across a range of GxP environments, including:
We support GLP organisations with independent QA oversight across non-clinical research activities, including:
Study based audits
- Study plan & amendment review
- Critical phase audits
- Raw data & report audit
Process based audits
Facility based audits
- Independent audit of your QA unit
Computer System Validation (CSV) audits
Regulatory and vendor audits
- Mock inspections
- Live inspection support
QMS documentation support
- Sops
- Policies
- Standard forms & templates
Ad hoc consultancy services
- General advice and support on quality assurance and regulatory matters
Our GLP audit specialists have experience across a broad range of disciplines, including toxicology, genetic toxicology, developmental and reproductive toxicology, bioanalysis, pharmacokinetics, metabolism, immunohistochemistry, ecotoxicology, environmental fate, residue studies, biocidal products and ISO 10993.
Our GMP QA support helps organisations maintain effective pharmaceutical quality systems and manufacturing oversight.
Routine QS activities
- CAPA management, investigation co-ordination, document control
Internal audits
- Tower Mains can assist with the planning, conduct & review of these audits as applicable
Ad hoc consultancy services
- General advice and support on quality and regulatory matters
Regulatory and vendor audits
- Mock Inspections
- Live inspection support
QMS Documentation Support
- SOPs
- Policies
- Standard forms & templates
We support clinical research organisations, sponsors and service providers with practical GCP QA support across the clinical development lifecycle.
Routine QS activities
- CAPA management, investigation co-ordination, document review & control
Investigator site support & advice
Internal audits
- Tower Mains can assist with the planning, conduct & review of these audits as applicable
Regulatory, investigator site and vendor audits
- Mock inspections
- Live inspection support
QMS documentation support
- SOPs
- Policies
- Standard forms & templates
Ad hoc consultancy services
- General advice and support on quality and regulatory matters
Why choose Tower Mains?
Global GxP Expertise
Access experienced auditors, quality professionals and subject matter experts across the GxP landscape, from clinical and laboratory environments to manufacturing, devices and research. We bring industry experience and specialist insight to help you address quality and compliance priorities.
Regulatory and Technical Insight
Our team brings extensive, real-world experience across global regulatory frameworks, including ICH, FDA, EMA and MHRA requirements. We help organisations interpret regulatory expectations, focus on what matters, assess risk and make informed quality decisions with confidence.
Flexible Quality Solutions
From single audits and annual audit programmes to vendor oversight, QA support and inspection readiness, we provide the right support for your objectives and risk profile. Services can be delivered in person, remotely or through a hybrid approach.
Practical. Proportionate. Collaborative.
We believe quality should enable your organisation, not add unnecessary complexity. Working alongside your teams, we bring an objective perspective, provide constructive challenge and help strengthen quality systems through sustainable improvements.