Your Partner in Quality Compliance and Regulatory Excellence
QARA is a premier quality and regulatory consultancy specializing in the life sciences sector. With over 15 years of expertise, we provide tailored, risk-proportionate advice and support to meet your specific needs.
With a deep-seated passion for problem-solving and a commitment to excellence, we leverage over 15 years of expertise in Good Clinical Practice (GCP) and Good Pharmacovigilance Practice (GVP).
Our firm provides risk-proportionate advice and support to life-science organizations, catering to small start-ups, international corporations, and public sector entities alike.
Our services are designed to be flexible, engaging on a temporary, ad-hoc, or retainer basis to meet diverse client needs.
Discover more about our extensive range of professional services by clicking on the below buttons.
QMS development
SOP Universe
Training Universe
Deviation Management
Audit & Inspection
Submission Advice & Planning
Technical Writing
Ethical & Regulatory Approvals
Our mission is to deliver superior quality and regulatory services that empower our life-science clients to optimize their efficiency and effectiveness while maintaining the highest standards of compliance and quality.
We achieve this by employing a solution-focused, risk-adapted approach. We engage with all relevant stakeholders to understand their unique needs, ensuring clear and continuous communication to facilitate adaptability and flexibility.
We maximize value for our clients by optimizing available time and resources while upholding quality and compliance.
We design risk-based and flexible solutions tailored to our clients' specific needs.
With a resolute can-do attitude, we consistently deliver on our commitments, ensuring reliability and trustworthiness.
With over 15 years of dedicated experience in the clinical research sector, we have cultivated a profound understanding and unparalleled expertise. Our consultancy services are rooted in this extensive background, ensuring we deliver exceptional quality and regulatory compliance.
Skilled in regulated interventional clinical trials (Phase I, II, III, IV, crossover, and OLEs), non-regulated interventional studies (incl. surgical, questionnaire), and non-interventional projects (RWD, clinical audits, Delphi projects, etc.).
Comprehensive experience in oncology (incl. colorectal, breast, testicular), neurology, paediatric, maternal health, and rare diseases.
Proven track record in national (UK) and international settings, including Europe (CTIS countries & Switzerland), the US, Canada, Australia, and New Zealand.
Proficient in electronic/remote consent, electronic Participant Reported Outcome Measures (ePROMs), electronic Clinical Outcome Assessments (eCOA), home healthcare services, IMP delivery, and more.
Telephone: +44 (0)74 263 263 63
E-mail: admin@qaraconsultancy.com
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QARA Consultancy LTD. Registered in England and Wales. Registered Address: 86 Melling Road, Liverpool, L9 0LQ.
Company Registration No: 16188234. VAT Registration No: 485 3538 58.
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