Service Description

CRO Clinical Trail and SAS Consulting ​ Services Scope: Our teams are ready to work for you! We are focused on your issues and we’ll bring the solutions right to you ​ ​ Project Management - AVTECH’s global clinical trial management, can provide expertise in many therapeutic areas at all developmental phases of research in both drugs and devices. Clinical Trial Management - AVTECH’s expert data management team with experience across a wide range of therapeutic areas and high level of attention to detail will custom-design your paper-based case report form (CRF) or electronic data capture (EDC) or ePRO systems to suit your trial, protocol and budget. CRF Design & Data Capture - our highly experienced team of statisticians can provide statistical and biostatistical analysis, SAS programming, database setup, statistical input into clinical trial design, sample size calculations, and more. Statistics - delivering expertise and excellence in electronic and paper CRF design, data entry, development of data management plans, data cleaning, coding of adverse events, medical history and medication and data listings. Clinical Data Management - an experienced team of PhD and MBBS writers can provide medical, scientific and academic writing including clinical trial protocols, Investigator Brochures, ethics submissions and informed consent documents, clinical trial reports, publications, promotional material (including presentations), and more. Medical and Scientific Writing - AVTECH's independent Quality Assurance team has decades of industry experience, and performs audits of internal systems and processes, departments, and study related services and procedures.

Contact Details