StatPlus Service
StatPlus Service
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At StatPlus, we offer comprehensive services in the areas of Drug Development, Medical Device, and Clinical Research. Our services cover the entire spectrum of the development process, from Project Management, Medical Writing, and Regulatory Affairs to Medical Monitoring, Monitoring & Site Management, Data Management, and Biostatistics. Our team of experts has extensive experience in these areas and can provide tailored solutions to meet your specific needs. By entrusting your project to StatPlus, you can be confident that we will help you navigate the complex regulatory landscape and streamline the development process to bring safe and effective therapies to market.
Drug Development
Clinical Development Plan
IND Submission
Phase I-IV Clinical Trials (including PK/PD)
NDA Consultation
Post-Marketing Surveillance
Clinical Research
Outcome Research Study
Epidemiology Study
Medical Device Clinical Study
Class II&III Medical Device Clinical Trials
In Vitro Diagnostic (IVD) Clinical Trials
Clinical trials, vital research studies, evaluate the safety and effectiveness of new medical treatments and interventions. StatPlus plays a pivotal role in managing and conducting these trials, customizing their services to meet clients' specific needs, ensuring efficiency and compliance with rigorous standards.
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