Quality

Academy Clinical Research

Specializing in Phase I—IV Clinical Trials

ACR ensures your Clinical Trials are compliant with ICH-GCP Guidelines from beginning to end!  We optimize the trial performance against such criteria as Time, Cost, Industry Acceptance and Service Level, while maintaining stringent high quality environments.

Quality is built in!!

Our commitment to quality is defined by our Quality Assurance Team. All studies conducted at ACR follow our standards within our Quality System:

Standard Operating Procedures (SOPs): ACR has a Solid SOP system established and implemented in all clinical trials, which ensures systems and processes are uniform and controlled.

Employee Training: ACR employees are rigorously trained on Good Clinical Practices (GCP), Good Documentation Practices (GDP), applicable SOPs and protocol-specific training prior to conducting clinical activities. As part of our commitment to quality, ACR staff members attend industry conferences on a regular basis to keep abreast of regulatory and quality requirements.

Auditing: Audits are conducted during multiple stages of the project to ensure compliance throughout the clinical program.

Text Box: SOPs
Text Box: Quality Control: 
ACR’s Quality Control team is trained in providing an objective review of all clinical documentation and data. All source data generated from a clinical trial is QC’d for completeness as well as protocol and SOP compliance.