A Clinical Research Organization (CRO) is a contract research organization that provides sponsors (pharmaceutical, biotechnology and medical device companies) with research management services. Traditional CROs provide clinical trial management services, while laboratory CROs provide drug discovery, manufacturing, laboratory and bioanalysis services. Sponsors often outsource these services to save resources in developing their new drugs. CROs offer organizations the opportunity to meet with experts and professionals in a particular field and have an in-depth conversation about the best processes that can be used, the potential problems that need to be addressed, and the optimal solutions to overcome them during the conduct of their clinical trials. We create comprehensive, yet efficient monitoring plans to manage clinical trials and build trust in the integrity of clinical trials. From clinical oncology research to vaccine development, successfully executing and monitoring the many moving parts of a clinical trial can be daunting for sponsors if they manage them on their own.
Developing methodologies that allow research to be audited throughout the clinical trial process saves time and resources. By outsourcing to a CRO, organizations can ensure that their staff is trained to carry out a thorough investigation. Professional quality control provides organizations with a means to ensure that their research and clinical practices conform to FDA standards. A contract research organization (CRO) acts as a bridge between the sponsor, who contracts the services, and the rest of the actors participating in the clinical trial. While the sponsoring company transfers the functions of the trial to a CRO clinical research company, the sponsor is responsible for the integrity of the trial and must ensure that the results are supported by facts and scientists.
The MED Institute is a contract research organization that provides comprehensive services and has more than 35 years of experience in the design and execution of clinical trials, ranging from initial feasibility studies to multinational, controlled fundamental trials and post-market registrations. In the late 1970s and early 1980s, when CROs were first created, they specialized in a specific service, such as statistical and data management services, regulatory support or clinical research monitoring. Developing continuous processes to define and track medical research problems is difficult and leaves organizations with less time to complete their projects. Working with a contract research organization can offer innovative tools that can increase efficiency and reduce time and costs. CROs are an invaluable resource for sponsors looking to save time and resources while ensuring that their clinical trials are conducted according to FDA standards. By outsourcing these services to a CRO, sponsors can rest assured that their projects will be completed efficiently and effectively.