Our goal is one thing - to help you bring high quality data to your clinical program so that more people can be helped by your therapy.
Together we will define a clinical strategy that is time and cost efficient, scientifically and clinically valid, and produces the data that will drive regulatory approval and adoption of your therapy.
Clinical Expertise Focused on Your Specific Needs.
OUR SERVICES
Project Management
Effective project management is what leads to meeting study goals from enrollment rates and timeline adherence, budget compliance, and most critically high quality data. Let our experience help you meet your study goals.
Clinical Strategy
It all begins with a well defined clinical strategy. It is critical to put together a strategy on how clinical data will be collected early in the development cycle. We can help you develop a Clinical Strategy that will lead your program through the various phases.
Resource Modeling
There are many ways to resource your clinical team from full-service CROs, fully resource internally, to some combination. We have extensive experience on both the Sponsor and CRO side and can use that experience to help you develop a plan and select the right vendors.
Scientific Advisory Boards
Having a strong Scientific Advisory Board (SAB) and utilizing it effectively can provide invaluable information for your product and clinical development. We can help you make the most out of your SAB and other advisory boards such as your KOLs and the DSMB/CEC.
Data Monitoring
Ensuring your data is clean and complete leading to evaluable data is the very purpose of your study. There are numerous tools and methods for performing clinical monitoring and data verification. We can help you evaluate all those options and develop the best plan for your study.
Medical Writing
Anchor Point Clinical can help you with writing activities including but not limited to protocols and associated documents, IFU/IB, manuscripts, annual and Clinical Study Reports, and clinical sections of regulatory submissions.