Protocol Preparation
We offer detailed, compliant research protocols tailored to your study requirements. Our team ensures clarity, adherence to ethical standards, and alignment with regulatory guidelines, enabling seamless study execution.
Deliverables
Complete research protocols, formatted for IRB/ethics review
Ethical compliance checks and guidance
Revision and refinement for final protocol approval
Our Process
1Initial Consultation
Define the research requirements, objectives, and regulatory needs.
2Drafting Protocol
Create a detailed, clear draft covering study design, methods, and compliance.
3Review and Revisions
Review the protocol, making revisions based on feedback and guidelines.
4Finalization
Finalize the protocol, ensuring it is ready for submission or implementation.
Timeline
4-6 weeks, considering the specific requirements and complexity of the study.