Smart-Start-60: Guaranteed Site Start-up Within 60 Days

• BRANY understands the importance of high quality, human subject research, and offers customized services to expedite the initiation of trials at any of our affiliate sites.
• The 60-day program includes: budget development, contract negotiations, completion of regulatory documents (including ICF modifications), and IRB submission and review.
• All of this, plus the convenience of a single-point of contact for rapid response and focused client support.
• According to Kimberly Irvine, Executive Vice President, Operations for BRANY: “Smart-Start-60 is an essential tool for sponsors and CROs to keep trials on schedule. Every day a study does not get up and running, is another day of missed milestones with significant budget impact.”
• On the occasion of the launch of Smart-Start-60, BRANY is offering new and returning clients an introductory rate.

Education and Training

We offer several educational programs through the BRANY Institute for Research Education. Our instructors include experts in the fields of research compliance and IRB standards. Options available both at your site and online

A choice of locations:

• Courses are offered at the BRANY offices in Lake Success, NY. We will also present any BRANY course at your facility.
• Who should take these classes? These classes are a must for any clinical research professional including principal investigators, research coordinators, research pharmacists, regulatory coordinators, and data managers who need to be familiar with the federal regulations, ethical guidelines, and processes involved in the conduct of human subject research.

Programs are offered in the following areas:

• Conducting Clinical Trials
• IRB
• Monitoring
• Finance / Budgeting

Selected BRANY Education programs are approved by the...
More Information » www.brany.com/hospitalsirbs/education-and-training

SMART- Technology Solution

BRANY's SMART system allows study sites to develop study budgets and conduct cost analyses utilizing pricing information stored within the database. Users can also manage and store regulatory documents.

This easy-to-use, online solution allows investigators and research staff to:

• Manage trial initiation, funding, and sponsor relations
• Assist in contract and budget development
• Handle accounting from start to finish, including holdback reconciliation
• Track investigators, subjects, and trial progress

The web-based software-as-a-service (SaaS) also allows clients to track completed subject visits and study procedures, revenue, and accounts receivable..