Clinical Trials Services
OV Clinical Trials (OV) is a clinical service organization designed to efficiently develop successful clinical research programs and implement clinical trials in both the clinic and in-home/alternate site settings (traditional and non-traditional). We specialize in "non-traditional/complex" clinical trials that require an extra level of support.Clinical Trial SOPs
Clinical Trials Standard Operating Procedures are intended to support compliance with regulations and guidance that govern the conduct of clinical research. These clinical trials research SOPs establish standards for those responsibilities that regulatory authorities have attributed to the Investigative Site or Sponsor. Well-written and well-managed GCP SOPs provide an official way to consistently execute required research-related activities. In addition, they can improve communication among staff, reduce dependence on individuals with institutional knowledge, and improve efficiency of staff training. SOPs that establish standards of practice for how you will meet these responsibilities will help your company demonstrate to auditors and/or inspectors that you are aware of the regulations and guidance and have built the foundations of a good quality system for clinical trial.
Staffing Services
This division focuses on high quality Clinical Trials Staffing segment of the Clinical Research industry. We work with start-ups, mid-sized companies and emerging to Fortune 500 across Life Science, Pharmaceutical and Medical Device industries. Our team has a proven track record of helping companies attract and recruit some of the best and most talented candidates on the market. Our Account Executives take the time to listen to our Clients’ specific requirements and asses all aspects to provide a streamlined service that is tailored to their job description, budget, and timeline. Our in-house clinical trials technical experts are comprised of current and former pharmaceutical Research and Development professionals with project experience on large multi-national Phase I - Phase IV clinical trials. We leverage this expertise in the interview process to conduct a pre-screen interview assessing technical expertise. This process allows us to present candidates that are a fit on every level for our clients’ consideration.
CRO Services
OV consists of a multidisciplinary team with extensive Sponsor and CRO industry experience designed to efficiently develop successful clinical research programs and implement clinical trials in both the clinic and in-home/alternate site settings (traditional and non-traditional). We specialize in "non-traditional/complex" clinical trials that require an extra level of support across all phases of development. All critical operations in clinical trial set-up, management, monitoring, close-out, data management, biostatistics, medical writing, and quality management are carefully governed to ensure compliance with GCP/ICH, ISO, and FDA regulations and guidance. OV CRO consists of a multidisciplinary team with industry experience on the Sponsor side, CRO side, and home nursing side with expertise across all major diseases and industry disciplines. We have been extremely successful at completing clinical investigations of varying sizes, complexity, and scope in the pharmaceutical, biotechnology and medical device industries on tight budgets and timelines.
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