At QMED CRS, we are dedicated to providing exceptional support for global clinical trials and Investigator Initiated studies. We know that every research journey is unique and requires a personal touch, which is why we assign Clinical Research Coordinators (CRCs) to each research site with a focus tailored to individual protocols.
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We conduct thorough assessments to identify potential sites that meet the specific requirements of each study.
Read MoreOnce potential sites have been identified, we conduct site selection visits to evaluate their capabilities and infrastructure.
Read MoreWe provide guidance and support to sites in obtaining approval from local Ethics Committees or Institutional Review Boards (IRBs).
Read MoreOur goal is to ensure that all sites are audit-ready and capable of maintaining the highest standards of data integrity and participant safety.
Read MoreWe oversee that the collection, review, and processing of essential study documents at each site.
Our team provides thorough training to staff on study protocols, regulatory requirements, and data collection procedures.
Read MoreWe work closely with sites to develop and implement recruitment strategies to ensure timely enrollment of study participants.
Read MoreWe oversee the review of source documentation and Case Report Forms (CRFs) to ensure accuracy and completeness.
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