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Apr 25, 2013
ACRP Webinar - AE Reporting in the Era of Web 2.0: The Challenges of Having a Two-Way Conversation
Category: General
Date:        Thursday, 5/2/2013
Time:        6:30 pm - 8:30 pm
Location:   Saint Louis University
Health Sciences Center Campus
Salus Center
3545 Lafayette Avenue
St. Louis MO 63104
Room # 1503 - First floor

Symposium Cost
Registration fee:
FREE for ACRP Chapter Members
$10.00 for Non-members

CEU fee (paid in addition to registration fee):
$10.00 for ACRP members
$25.00 for Non-members

Sandwiches, chips, desserts and a mixed assortment of cold drinks will be served!

Registration:

Agenda:
6:00 pm      Chapter Meeting
7:00 - 8:30  Education Program w/ Q&A

Program Description:
This program will delve into how social media relates to the pharmaceutical industry.  See flyer on Google Sites Announcement for more details.

Speaker:
Elizabeth Garrard, PharmD, RPh
Chief Safety Officer
Drug Safety Alliance, Inc.

Upon completion of this course, participants should be able to:

1)  Grasp the importance of social media in today’s society and understand the difference between the top social media forums
2)  Describe two ways in which social media can create open, two-way communication with patients
3)  Explain why using social media is not likely to lead to an increase of reported adverse events
Jan 31, 2013
ACRP Presentation - Clinical Research Billing - Are You In Compliance?
Category: General
Date:        Thursday, 2/7/2013
Time:        6:30 pm - 8:30 pm
Location:   St. Luke’s Hospital
North Medical Building
Emerson Conference Room 1
222 S. Woods Mill Rd.
Chesterfield, MO 63017

Symposium Cost
Registration fee:
FREE for ACRP Chapter Members
$10.00 for Non-members

CEU fee (paid in addition to registration fee):
$10.00 for ACRP members
$25.00 for Non-members

This fee includes sandwiches, chips, desserts and a mixed assortment of cold drinks.

Registration:

Agenda:
6:00 pm      Chapter Meeting
7:00 - 8:30  Education Program w/ Q&A

Program Description:
This program will provide an overview of the major issues related to billing and compliance in the context of clinical research trials.

Upon completion of this course, participants should be able to:

1) Review compliance risks of clinical research billing
2) Discuss Contract and Consent language and the relationship to research billing
3) Demonstrate how to create a Coverage Analysis
4) Discuss Coding and how to find Medicare determinations
5) Discuss the bill review process and need for transparency
Jan 23, 2013
CTO's Q2 FY13 Report
Category: General
The CTO reviewed/executed 121 contracts:

1) Reviewed 70 New Contracts:

25 Clinical Trial Agreements,
21 Confidentiality Agreements,
16 Amendments,
7 PI Initiated,
1 Master Agreement;

2) Executed 51 Pending Contracts:

21 Clinical Trial Agreements,
11 Confidentiality Agreements,
7 Amendments/other,
11 PI Initiated,
1 Consultant Agreement.
 
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Welcome

The CTO supports innovative clinical investigative research at the Saint Louis University School of Medicine. Our office provides clinical trial management for industry sponsored trials, including the oversight of trials and input into their administrative, business, educational, regulatory, and operational functions.

The CTO streamlines the processing of both research study contracts and budgets with industry partners in order to facilitate the performance of clinical trials at the Saint Louis University School of Medicine.

The CTO also centralizes important administrative functions and establishes standard policies and procedures needed for the successful management of clinical trials. This ensures the ease of use and proper documentation of all trial procedures, so as to improve efficiency and encourage coordination of research efforts between clinical Departments.

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Clinical Trials Office
Salus Center 
3545 Lafayette Avenue, 2nd Floor
St. Louis, MO  63104
Phone:  314-977-6335         ||          Fax: 314-977-4080  || clinical-trials-office@slu.edu