A CRO that offers a full suite of services and that can manage all of your phase I to IV clinical trial needs offers you the most reliable chances of success. Their methods should be integrated with your existing team and processes, and provide collaboration to help you achieve your desired results. Employing a company with experience in rescuing studies is also a good reassurance to have on your side. Here are three tips to ensure you get optimal clinical trial solutions that work. 1. Early Phase Experience to Get You Started The CRO should be able to demonstrate successful experience in pharmacodynamics and pharmacokinetic studies, and under most routes of administration, as well as the most important therapeutic areas. Most new companies can demonstrate experience and proficiency in this area, but the more extensive the experience is the more assistance the CRO can offer you later down the line. 2. Phase II and III Experience to Carry You Through To Completion Your CRO should have experience with small, regionally located trials and complex global studies. It is also helpful if they can show focus in areas like minimizing risk, improving cost and time efficiencies and provide ways to optimize performance tactics to ensure that the essential milestones are reached. They should be budget focused and provide good management guidance to ensure that the necessary parameters are worked within and that deadlines are adhered to. The CRO should also have extensive site management experience as well as a strong focus on safety matters. They should integrate their technology with your own and deliver comprehensive reporting solutions. It is ideal if they have a global CRO network if your study falls outside of local borders. Companies with experience in saving projects are also invaluable to have on your side, especially if your team is handling the biggest share of the work. This means that if you find your team is not delivering and will not be able to complete the study on deadline, you have a contingency plan to fall back on. 3. Post Approval Expertise Post approvals are time-consuming, but they can be very lucrative when they are done properly. The CRO should have experience in regional and national-scale studies, as well as working on international programs. The CRO should offer assistance with drug registrations and be able to provide a comprehensive follow up service that lets you know where they are in the process every step of the way. For more information about the clinical trial solutions, please visit our website.
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