Clinical Project Management (CPM)

Trial Coordination: Manage all phases (planning, execution, monitoring, closure)
Protocol Oversight : Ensure compliance with GCP and regulations.

Sponsor-Omikare I&F Concept

Decentralized Clinical Trials (DCT)

Technology Integration: Help sponsors deploy digital tools (telemedicine, remote monitoring)
Site Coordination: Facilitate team and patient management at decentralized sites.

Medical and Regulatory Writing (MRW)

Protocol and Amendment(s) Writing: Prepare essential documents for regulatory submissions.
Clinical Report Writing: Provide study reports and scientific publications.

Clinical Data Management (CDM)

Data Handling: Provide expertise in clinical data analysis and safety compliance.
Data Assessment: Partner in statistical data interpretation for clinical trials.

Compliance & Audit (C&A)

Trial Audits: Ensure trials meet international and local regulatory standards.
Regulatory Submissions: Provide guidance for trial submissions to health authorities.

Training & Strategic Consulting (TSC)

Team Training: Deliver workshops on GCP, data management and compliance.
Strategic Consulting : optimize clinical trials and develop new research initiatives.

Niche Specialization

Gene therapies, immunotherapies, neurology and oncology trials.