In today’s environment, drug developers must decide whether to leverage a contract research organization (CRO) partner even earlier in their development timelines. It’s estimated that nearly three out of every four clinical trials today are conducted by contract research organizations (CROs), highlighting just how much sponsors value – and rely on – the work that CROs perform. In today’s competitive landscape, with early decision and engagement, CROs enable their customers to navigate and overcome resource challenges. This is where companies like Everest Clinical Research come in.

Everest clinical research is a full-service contract research organization (CRO) offering the global pharmaceutical, biotechnology, and medical device sectors a comprehensive variety of expertise-based clinical research services. Everest works with several of the most cutting-edge pharmaceuticals, biologics, and medical devices now in development and services some of the most well-known firms. Everest, which was established in 2004, has a solid reputation as a center of excellence for statistics and data management. Everest has effectively grown and established itself as a full-service CRO by building on this basis. Operating primarily in North America, with headquarters located in Toronto, Ontario, Canada, a second office in Little Falls, New Jersey, USA, and a third office in Shanghai, China, Everest is known in the industry for its high-quality deliverables, superior customer service, and flexibility in meeting clients’ needs.

Everest Clinical works with many of the most cutting-edge medications, biologics, and medical devices currently being developed and conducts research with some of the world’s most well-known pharmaceutical, biotechnology, and medical device firms. The organization’s base is excellence in biometrics services, and it has developed into a full-service Contract Research Organization (CRO) that is information-driven, quality-focused, and data-driven. Promotes high-quality standards, is customer-focused, has a can-do attitude, uses cutting-edge technology, aims for continual progress, and has a high standard of ethics and professionalism. expands to effectively provide customer service and serve as a hub for Everest’s clinical research services. Provides clients with excellent industry experience and a track record to help them meet their goals for developing drugs and medical devices.

Everest Clinical Research’s Biostatisticians and Statistical Programmers offer years of industry experience, therapeutic knowledge, and familiarity with regulatory requirements to assist you with a full range of biostatistical and programming services. Excellence in clinical data management, from trial case report form (CRF) design through database lock, is the cornerstone of Everest. Many clinical trial sponsors have used the phrase “execution excellence” to describe their interactions with Everest’s clinical data management services. For the administration of clinical trial data, Everest provides both paper/fax-based and electronic data capture (EDC) systems that are scalable and reasonably priced. Everest provides the following data management services. Clinical data management services from Everest are delivered by ICH, GCP, and regulatory agency criteria, utilizing regulated and secure computing environments, validated software, and systems that comply with 21 CFR Part 11. Everest uses standard operating procedures, such as templates for standard CRF/eCRFs, data management plans, user acceptance test plans, data review checklists, database quality acceptance sampling plans, database lock checklist sign-off sheets, etc to increase efficiency and ensure quality. Everest’s statistics and data management teams have a lot of expertise supporting the work of the Data Monitoring Committee (DMC) and Data and Safety Monitoring Board (DSMB). The DMC/DSMB Administrators at Everest effectively communicate with the trial sponsors, statistical/data management teams, and committee members. Every DMC/DSMB activity previously has gone off without an issue.

Subject randomization and medication supply for the clinical trials are efficiently managed using interactive web-based response system (IWRS) technology. Everest has a long history of employing online technologies to facilitate efficient multi-country clinical trial management. Everest’s web technology and statistical expertise may be used to create and put into practice a variety of randomization schemes and medication supply management strategies, ranging in complexity from simple to complicated. IWRS is a superior option over interactive voice-response systems (IVRS) for trial subject randomization and medication supply management since it has a standard web browser, comprehensive and adaptable functions, as well as an intuitive and self-explanatory user interface. Everest has expanded on a history of offering high-performing statistical and data management services to become a full-service Contract Research Organization (CRO) that is driven by data and information and prioritizes quality and client service. The efficacy and efficiency of clinical trial design, management, and site monitoring are currently being improved by Everest by using its capabilities in enabling data collection and carrying out data quality management. “At Everest Clinical Research, we strive for excellence, embracing the opportunities to make a difference and inspire positive change.” – Irene Zhang, President and CEO of Everest Clinical Research.” Everest Clinical Research is a company with a strong track record of success and a clear vision for the future, making it a reliable partner for businesses looking to take their CRO to the next level.