Leverage Expertise with WCCT Global for Your Phase 1 Clinical Trial

1. Leverage Expertise with WCCT Global for Your Phase 1 Clinical Trial

2. Leverage Expertise with WCCT Global for Your Phase 1 Clinical Trial When it comes time to perform Phase 1 clinical trials for your product development, rely on WCCT Global’s expertise. With their experience, your SAD/MAD, PK/PD, BA/BE, device, and first in human clinical trials first in human clinical trials, your trial will be in capable hands. As a contract research organization, WCCT is an ideal partner to help start-up biotech and large pharmaceutical companies alike. WCCT has specialized regulatory and clinical professionals at the ready to offer an innovative, collaborative, and agile approach to every clinical trial. Here are some of the areas of expertise which WCCT can offer its partners. Proper Participant Recruitment Proper Participant Recruitment A proper participant recruitment method is crucial to a successful Phase 1 clinical trial. If your start-up does not have the proper inclusion and exclusion criteria, you may not have a suitable participant pool for your trial. WCCT can help you manage the study design, standard of care, and more. They can help determine whether more advertising is needed, such as for overnight studies. WCCT will manage stipends and participant expectations, as well. Ethnobridgin Ethnobridging Expertise g Expertise One of WCCT’s specialties is conducting trials utilizing Ethnobridging They are specifically adept in trials with participants of Asian descent (Japanese, Chinese, Korean, etc.). WCCT recruits about 750 new Asian participants annually and Ethnobridging as a strategy.

3. maintains a database of more than 9,000 Asian participants. Ethnobridging in Phase 1 helps promote a reduction in cost and development time. This allows for recruiting patients in a “global” manner without the need for leaving the country as in phase 2 and 3 efficacy trials. Using Ethnobridging as a strategy can also alleviate the need to repeat Phase 1 studies in Asia. Resources, Facilities, and Equipm Resources, Facilities, and Equipment ent WCCT has the resources and equipment necessary to carry out a variety of Phase 1 clinical trials. With phase 1 clinical trial units phase 1 clinical trial units in their 75,000-square-foot facility, containing 180 beds, in Southern California, WCCT already has the proper clinical trial space. They also offer an on-site, CLIA-certified and CAP-accredited Safety Reference Laboratory and a pharmacy with a USP-797 compliant clean room for sterile drug preparation. . Handling Research Services Handling Research Services WCCT offers the expertise in handling research services, as well. These include regulatory support, protocol development, medical writing, project and data management, clinical monitoring and biostatistics, and medical monitoring and safety. These items can be stand-alone or full-suite, all offered at their facility. Trained Staff Trained Staff Project Managers are recruited specifically for their proven experience in managing trials in a Phase 1 setting. Clinical staff are trained in emergency response, and have various levels of licensure that will be needed to competently perform procedures in Phase 1 trials. WCCT can ensure regulatory documents are accurate, complete, and follow any sponsor requirements with trained staff. Their experienced medical writers will plan and produce clinical protocols for the project, as well as study reports and overview documents. Start your Phase 1 clinical trial https://sponsor.wcct.com/ https://sponsor.wcct.com/ Original Source: https://bit.ly/3d2DL9G with WCCT as your partner at