SERVICES

OVERVIEW

With more than 12 years experience conducting clinical trials in the rapidly developing markets of Latin America and South East Asia, our unit in Bangkok has developed as our centre of operations.
From here we are able to provide high level, GCP compliant, clinical research, in close co-operation with the largest university hospital in Thailand.
ACLIRES has performed trials for an international array of biotech companies as well as for some of the largest global pharmaceutical companies. With our broad access to patients and expertise, our aim is to rapidly initiate our client’s studies, even when a very special patient population is required.
A dedicated project manager or study coordinator is assigned to all studies to monitor, manage and communicate the status of the project, while our Professional Quality Management function assures the highest quality standards.
Early Phase
  • Study coordination
  • Combined protocols (SD/MD)
  • Discussion with experts
  • Recruitment of healthy volunteers
  • Recruitment of special patients
  • Regulatory services
  • Drug importation and labeling
  • Performance within a state-of-the-art research unit
  • Monitoring
Late Phase
  • Site selection
  • Site management
Feasibility
  • Regulatory services (including reporting to authorities and ECs)
  • Drug importation and distribution
  • Investigator meetings
  • Project management
Recruitment
  • Support for sites
  • Call center
Regulatory
  • Consulting
  • Preparation of all submission documents
  • Contact to IRBs
  • Drug importation
Monitoring
  • Preparation and presentation for investigator meetings
  • Organization of initiation and close out visits
  • On-site and remote monitoring
Site selection
  • Feasibility studies
  • Site management
Scientific Services/Medical Writing
  • Research
  • Protocol Writing
Quality Management
  • Quality surveys
  • SOP management
  • Preparation, follow up and performance of audits