LANE millett clinical research consulting
INCREASING clinical research site efficiency & PRODUCING higher quality data for sponsors
SERVICES
TRAININg
Site efficiency training, Coordinator and PI GCP and ALCOA+ training
SOURCE DOCUMENTS
Source document creation, including updates for protocol amendments
MONITORING
Site monitoring, efficiency recommendations, and help to implement these recommendations
SOP CREATION
Ensuring site SOPs are in accordance with GCP and FDA guidance
QUALITY OVERSIGHT
Ongoing internal quality oversight is a critical aspect of staying inspection ready
LANE MILLETT
Hello, I'm Lane. I've worked in the clinical research industry as a Coordinator, Site Director, and CRA, for both Sponsor and CROs for the past 10 years and have been exposed to many styles of conducting clinical trials.
In order to level the playing field for sites with less experience and fewer internal resources, I have launched this consulting firm to address the inconsistencies that are commonly present at sites. My goal is to help give your site the resources and training to run efficiently and focus on patient safety.
Let's get started today, email me at lane@lanemillettconsulting.com or fill out the form below.