Falcon Consulting Group, LLC has demonstrated reliability and great success in the delivery of a diverse and unique portfolio of Good Clinical Practice (GCP) services. We work collaboratively with our clients to create a beneficial working relationship that allows us to provide appropriate and customized clinical trial auditing support, and assistance in the development of Clinical Quality Assurance (CQA) programs and infrastructure. Falcon offers Global GCP services that complement typical clinical trial auditing that include: advisory consultation and development of optimal processes, workflow and standards for the conduct of clinical trials; mock regulatory inspections; safety surveillance support; trial master file inventory and management electronic and paper; virtual Clinical QA services; high level clinical project management; and GCP training.
The Good Clinical Practice (GCP) Services group distinguishes itself with its large team of full-time Falcon employees who are highly experienced Quality Assurance(QA) Professionals. Our GCP team has an exceptional level of knowledge, with diverse skills and expertise, having met high-level Falcon employment requirements. The breadth and depth of our team members’ experience is extensive, with many previously serving in industry management roles. Our team has provided services to a wide variety of clients, from small start-up firms to fully-integrated global pharmaceutical, medical device and bio-tech firms, as well as government agencies. In addition, language capabilities in this group currently include: Russian, Spanish, Greek, French and German.
The Falcon GCP Services group promotes a philosophy of independent, preventative and proactive quality assurance. We place a strong emphasis on the concepts of good quality control, with adequate documentation throughout the conduct of a clinical trial by investigators and throughout all data management processes leading to a regulatory submission. Our primary focus is to assist our clients in the implementation of GCP quality strategies that support compliance and minimize regulatory risk while being flexible in our consulting approach and service offerings. Foremost, we advise our clients on procedures that protect the safety and welfare of clinical trial subjects. We assist our clients with procedures for regulatory compliance using our knowledge of industry “best practice” while also considering practical logistics, business efficiencies and applying “common sense” when helping our clients develop quality solutions.