About

About EPIC-CRO Research EPIC RESEARCH CRO "We are focused on providing a full range of tailored, efficient, high-quality, and cost-effective clinical development, regulatory, and post-approval services to the Pharmaceutical, Biotech, Medical Device, and Nutriceutical industries. At EPIC, we help develop and bring new molecules and developments to the regulatory process through trial design, management, site selections, CRFs, ICF, and other material developments emphasizing collaborative work with your team and our clinical and regulatory experts to ensure cost-effective results." About EPIC-CRO Research EPIC RESEARCH CRO "We are focused on providing a full range of tailored, efficient, high-quality, and cost-effective clinical development, regulatory, and post-approval services to the Pharmaceutical, Biotech, Medical Device, and Nutriceutical industries. At EPIC, we help develop and bring new molecules and developments to the regulatory process through trial design, management, site selections, CRFs, ICF, and other material developments emphasizing collaborative work with your team and our clinical and regulatory experts to ensure cost-effective results." Clinical trial planning and design: We can help you develop and bring your trial strategy and design to life through collaborative work with your team and our clinical and regulatory experts to ensure cost-effective results. Phase I-IV: From single site to multi-site and multi-national trials, we have the expertise to conduct your trials successfully. Protocol development: Our team of experts will design a protocol that will meet all your clinical development needs for any phase of study. Clinical monitoring: Our clinical research associates receive expert training to ensure that your clinical trials are conducted in strict accordance with the protocol, GCPs and all applicable regulations. Regulatory Affairs: Our team of regulatory experts will handle all regulatory procedures with Ethics Committees and Regulatory Authorities from study start up to study close out. Safety and Pharmacovigilance: Our staff will take care of all requirements for AE and SAE reporting to Ethics Committees and regulatory authorities, as well as annual safety, final reports and DSURs Trial Feasibility Assessment: As time goes by clinical trials become more complex along with subject selection criteria, in a collaborative effort we can help you determine your trial’s feasibility and make the necessary adaptations in the design to ensure your study’s success. Early phase services that include: Design and execution of pre-clinical trials, Phase I protocol development and execution, medical writing, monitoring, data management, biostatistics and clinical pharmacology.