Assurance of quality
PCG is characterised by a very experienced staff, taking care of the whole spectrum of your clinical development needs. PCG has performed more than 120 clinical studies since the inception of the company. We believe that efficient project management is the essence of the successful performance of a clinical trial.
The founders of PCG have extensive knowledge in the design of clinical trials, including the statistical considerations, recruitment of study sites, monitoring, data handling and project management.
The PCG edge:
PCG provides extremely efficient management of your clinical trials in the Viedoc™ system. Viedoc™ is an intuitive, user-friendly, powerful, 21 CFR Part 11 compliant web-based software that allows clinical trial sponsors and investigative sites to easily and securely collect, validate, transmit and analyse clinical study data. It is a proven application and has been used globally for over one hundred trials on a broad spectrum of study types, from phase I to post-market surveillance and patient registries for a wide range of clients. Not needing to buy and install the software at the site means a faster and better study set-up and lower costs. Study set-up, training, administration/support and related services are of course included in the price.
Viedoc™ also enables efficient sharing of information, project management and monitoring of study activities and sites. It is highly appreciated by the most important persons in the clinical trials - the investigators and study nurses. The sponsors are always on top of the study when using Viedoc™.
Some examples of features & functionality:
Please visit us at www.pharmaconsultinggroup.com for more information!