Innomas clinical research

At Innomas Clinical Research, we provide end-to-end support across the clinical trial lifecycle, combining global expertise with a strong foundation in quality management to deliver exceptional results.

Regulatory & Ethics Consulting

Submission preparation and regulatory liaison

Compliance tracking and reporting

Ethics committee setup, training, and process improvement

Medical Writing & Publications

Authoring protocols, investigator brochures, and clinical study reports

Developing manuscripts, abstracts, and regulatory documents aligned with global standards

Clinical Data Management & Biostatistics

End-to-end data management solutions designed to ensure data integrity and compliance at every stage of your clinical trial. Our Nigerian-based offshore clinical data management team offers a cost-effective, high-quality service tailored to meet global standards.

Key Services Include:
Data Review and Cleaning
Protocol-Specific CRF Design
Database Management
Statistical Analysis

Pharmacovigilance

Experts available to set up PV system operational and support services: EU QPPV, local affiliates, QMS, Audits, PV training and Compliance etc. Clinical trial drug safety management: Full GCP, GVP, GMP and GDP. PV experts are ISO 9001:2015,ISO 14001 and ISO 18001 certified.

Post-Market Surveillance & Real-World Evidence
Monitoring product safety and effectiveness after regulatory approval

Supporting compliance with post-marketing requirements and pharmacovigilance.

Clinical Operations, Trial Management and Training

Clinical Operations & Trial Management
Study design, site selection, and initiation
Patient recruitment and retention strategies
Monitoring and compliance oversight
Vendor and site management

Training & Capacity Building
Customized training for research teams and stakeholders on quality principles, including quality culture development and proactive management practices

Workshop-style sessions to foster continuous improvement

Quality Services

Delivery of high-quality, regulatory-compliant solutions that uphold the integrity of clinical trials end-to-end with a tailored quality-driven approach tailored to meet specific needs and address complex challenges.

Core Services
Quality by Design (QbD) Consulting, Risk-Based Quality Management (RBQM), Clinical Trial Risk Assessments, GCP Compliance Audits and Gap Analysis, Clinical Quality Management Systems (CQMS), Inspection Readiness and Mock Audits, SOP Development.