Management Solutions
Study Start- Up
Our Study Start-Up Management services are tailored to provide a seamless and efficient start to your clinical trial. We handle every aspect, from site selection and regulatory submissions to contract negotiation and ethics committee approvals, to streamline the initiation process. Our expertise helps minimize delays, ensuring your study is set up for success from day one.
Regulatory Submissions
With ELS's Regulatory Team, you can rest assured that your study receive comprehensive support from start-up to close-out. Our team's deep expertise in IRB management, coupled with strong relationships with leading IRBs, ensures that your submissions are processed efficiently and in alignment with your overall study strategy.
Data Management
Our Study Data Management services are designed to provide, secure, and reliable clinical trial data. We offer a range of services, including database design, data entry, validation, and reporting, using advanced tools and best practices. With our precision and care, we help ensure reliable outcomes and regulatory compliance throughout your trial.
Trial Management
Ethos Life Science's clinical trial management team provides support for efficient trial execution. Our flexible approach aligns with your needs. Our customizable CTMS simplifies study tracking and management, while integrating with EDC streamlines workflow.
Trial Rescue
Assembling the right team to address challenges is crucial for a successful trial outcome. At ELS, we leverage our extensive knowledge and experience to deliver effective solutions for trial stabilization. Our skilled and adaptable team uses evaluation tools to assess study operations, identify key issues, and offer strategic guidance to steer the clinical trial toward success.
Medical Writing
Our medical writing services encompass a wide range of offerings, including:
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Protocol Development and Amendment
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Abstract Preparation
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Manuscript Writing, Preparation, and Review
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Scientific Reviews
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Clinical Study Report Writing