Trimanos - Lending Business a Hand
Trimanos services are specifically designed to help sites wanting to start clinical trials for the first time, or sites coming back to clinical research after a break. There are four main steps:
1. Getting Ready
2. Getting Started
3. Tune Up and Audit
4. The Trimanos System
Trimanos can take you through these steps
- face to face, online, or both - to the point when you are
up and running with your first trial. If you want to work with
us after that, we are available to help. And our on-line support
- the Trimanos system - stays with you, whatever.
Trimanos is independently owned and financed. It will be happy
to work with sites and sponsors alike; but it is not funded
or influenced by any third party. So you can work with us in
full confidence that we are committed to the best interests
of your site, your patients and your sponsors.
1. Getting Ready: Readiness Audit and Startup Plan
When you start out in clinical research, you need to assess:
staffing and experience
physical resources
operational procedures
permissions and relations with the IRB
impact on other activities.
Trimanos can do a readiness audit and deliver you
a simple start up plan for you and your team to consider. If you
adopt it, we can then assist you with implementation, and winning
your first contract.
2. Getting Started
What makes or breaks many sites is their capacity to work well
with the Sponsor. Trimanos can help you first find a Sponsor,
and then make a success of working with them - including making
sure you get paid.
3. Tuning Up and Audit
Trimanos can also assist experienced sites who want to review
and refresh their administrative structure.
4. The Trimanos System
Written
under the editorial direction of the General Editor Dorothy Adams
Farnham, with over twenty-five years experience running a multi-specialty
research site, the Trimanos system offers you on-line access to
the knowledge and the tools you need to make a success of your
trials. Mouse-click access to:
Working with patients
Working with sponsors
Recruitment and advertising
Informed Consent
Scheduling
Documentation
GCP compliance
Storage and handling of test article
Reviews and Audits.
Even down to the individual SOP, Trimanos is crafted
to be adaptable to the needs and culture of your site, while keeping
you on track, and in compliance with all the regulatory requirements
of Good Clinical Practice.
Use it for management, for reference, for training and for compliance
with GCP.
Downloads
Download this leaflet at www.trimanos.com/resources/pdfs/trimanos-leaflet-services.pdf
Contact us if you need help with:
- Setting up your site
- SOPs
- Compliance
- Job descriptions
- Patient recruitment
- Task templates and work flow
- Financial management and controls
- Sponsor relations
- IRB and Ethics Committee
- Winning business from sponsors
- Facing an audit