• About Us

Company Profile

QualiClinic recognises that the management of Quality is an integral part of its operations.

QualiClinic (QC) is a private Hungarian SMO (Site Management Organization) – a company managing clinical trials for pharmaceutical and medical device industry.

The company is located in the 13th district and operates as a well-equipped, private healthcare facility providing services in various areas of medicine, where patients receive high-quality care.

Our experienced specialists are supported by well-trained and experienced site staff in the professional management of patients enrolled into the clinical studies.

Our activities are focused on site management services for Hungarian and international pharmaceutical companies, medical device developer companies, global CRO-s and other health institutions. Our clients are guaranteed to work with highly qualified site managers and study coordinators who are well experienced in clinical trials.

By consistently following the ICH-GCP and the relevant international and Hungarian guidelines and laws, as well as by strictly adhering to the deadlines, we are trying to win the confidence of our customers.

QC was founded in 2010 and started to work in cooperation with another SMO, Cortex Study Center in 2024.

QC is in an exceptional location, available for clients and patients at a charming, easily approachable part of Budapest in a European level environment.

We are reaching our goals by combining medical expertise and clinical trial experience.

Quality Policy

QualiClinic recognises that the management of Quality is an integral part of its operations. The company views this aspect of management as a primary responsibility and that the key to good business is the adoption of appropriate Quality standards.

The company Quality policy calls for continuous improvement in the company’s Quality management activities and for its business to be conducted according to the following principles:

  • Comply with all applicable directives, laws, guidelines and regulations related to clinical trial management
  • Follow all related standard operation procedures of client and Cortex as applicable
  • Ensure that any client requests for assistance are dealt with promptly and effectively agreed in accordance with the terms and conditions of signed contracts
  • Seek at all times to ensure that our services meet the highest standards of quality and cost effectiveness
  • Follow a concept of continuous improvement and make best use of our management resources in all Quality matters
  • Take due care to ensure that activities are safe for employees, associates and subcontractors and others who come into contact with our work
  • Take due care to ensure that activities are safe for employees, associates and subcontractors and others who come into contact with our work
  • Work closely with our clients and vendors to establish the highest Quality standards
  • Adopt a forward-looking view on future business decisions which may have an impact on Quality
  • Train our staff in the needs and responsibilities of Quality management
  • It is also our aim that, with the total involvement and understanding of all staff through the implementation of a documented Quality Management System, we will exceed the expectations of our Clients and staff.

Our mission is the accurate implementation of our Clients’ clinical trials plan

  • with, following the relevant local and international legislation, guidelines and the highest professional-ethical requirements
  • ensuring the rights, well-being and maximum safety of patients
  • guaranteeing excellent data quality
Our services