CLINICAL
MONITORING
MONITORING
Patient Safety and Data Integrity
Nothing is more important than insuring subject safety during your clinical trial. Our comprehensive monitoring plans, extensive SOPs, and experienced Clinical Research Associates (CRAs) ensure compliance with domestic and international regulations and guidance.Our CRAs have experience working in the medical industry as RNs, LPNs, or MDs and are proficient in managing the development, coordination, and implementation of clinical operations site management.
Achieving Compliance
| Our CRAs will assist you in developing and revising your protocols and protocol amendments |
| Our CRAs will develop monitoring plans |
| Our CRAs will develop your project scope of work |
| Our CRAs will develop operations manual |
| Our CRAs will develop, and maintain clinical trial documents, processes, and systems. |
Patient Safety & Data Integrity
ACE Research CRAs work closely with the rest of the clinical team to assure patient safety and data integrity at all times.
Experience Matters
| Experienced Staff in Sub-Saharan Africa countries |
| Capacity to trainin clinical site personnel |
| Experts in development of Monitoring Plan (Including frequency, intensity, and activity) |
| Experienced conducting Site Qualification, Initiation, and Close-Out |
| Complete Source Document Verification |
| Experienced in Regulatory Document Review and Collection |
| Expertise in Drug Accountability |
| Investigational Product Accountability |
