The QARP - Quality Assurance Research Professionals

The QARP provides expert guidance and support to pharmaceutical and biotech companies, Contract Research Organizations (CROs), and other healthcare entities and service providers involved in drug development, ensuring compliance with GxP and Regulatory Affairs in accordance with global standards. We evaluate overall compliance levels, address specific areas of concern, and offer tailored recommendations leveraging the extensive experience of our auditors. Our exclusive program includes interactive workshops, webinars, and online gamified and animated blended learning training sessions in clinical research. We cover a range of topics, such as both advanced and basic Good Clinical Practice (GCP), ISO 14155 for Medical Devices, the European Regulation on Clinical Trials and Medical Devices, Research Quality Management Systems, and GCP audit methodologies. Additionally, we design training programs specifically tailored to meet your unique needs. Furthermore, we perform GCP, GLP, GCLP and GMP audits through a team of seasoned professionals based across Europe (including Spain, the UK, Germany, Bulgaria, and Turkey), as well as in Israel, the Middle East, Australia, South America, the USA, and South Africa. We also provide support through our dedicated inspection preparation center, helping organizations ensure readiness for regulatory inspections.