Download Clinical Trial Resources in PDF Format

At Oxygen Clinical Research, we provide easy access to essential Clinical Trial Resources that support every phase of your research. These downloadable PDF documents are designed to help investigators, sponsors, and CROs manage trials more efficiently.

Our curated collection includes a wide range of clinical research documents, such as informed consent templates, AE reporting forms, and site logs. Moreover, each resource aligns with ICH-GCP and Indian regulatory guidelines, ensuring your trial remains compliant.

Whether you’re setting up a new study or handling ongoing responsibilities, these Clinical Trial Resources make documentation simpler and faster. In addition, they support consistency and accuracy across all research sites.

Here’s what you can download:

• Informed Consent Forms (ICF)

• Site Delegation Logs

• Visit Schedule Trackers

• Protocol Deviation Forms

• Ethics Committee Submission Templates

• Regulatory Binders

• Source Document Worksheets

Furthermore, our resources are regularly updated and reviewed by clinical experts to ensure they meet current trial standards. These documents serve as helpful tools to reduce protocol deviations, maintain audit readiness, and improve trial documentation practices.

Our goal is to help you focus on research, not paperwork. If you need customized formats or assistance in using any document, our team is ready to support you.

Explore the list of Clinical Trial Resources below and download the files that match your study’s specific needs. Your success in conducting ethical and efficient research starts here—with the right resources in hand.