佳捷生技股份有限公司

經營理念

SitePartner is a Site Management Organization (SMO) that was established in July 2004, we focus on enhancing site performance, conducting phase I-IV clinical trials with emphasis on patient recruitment and accelerating our clients’ drug development timeline. In today’s competitive market, we are cognizant that time is the real value and the recruitment is often the key to a successful outcome. Our core service is to assist our clients in bringing their product(s) to market faster with the site selection and support, and customized site-by-site patient recruitment programs. SitePartner is a high quality service organization that is able to provide flexible solutions to meet client’s needs. We offer professional services to the pharmaceutical, biotechnology, and CRO industries. We ensure adherence to study protocols, ICH GCP standards, SOPs and FDA regulations. Our senior management team has a combined 20+ years of experience in the patient recruitment industry. SitePartner can help your company to meet its timelines in the following areas: *Rapid site identification and qualification *Standardization among sites of clinical trial start-up and standard operating procedure *Timely patient enrollment and highest retention of valuable patients *Reduced time spent by project managers because of ongoing support from SitePartner *Minimal time spent monitoring high quality, professional sites *Placement of qualified and trained clinical research coordinator(CRCs) at study site Facilitating patient participation and compliance through SitePartner services supports your efforts to meet aggressive study completion and product-to-market timelines.