Central Northeast PA: Building a Robust Study Pipeline

Webinar Replay: Building a Robust Study Pipeline: Therapeutic Area Trends, Implications and Strategies for Clinical Research Sites

Program Agenda:

• 11:45pm -12:00pm – Registration. Feel free to bring lunch
• 12:00pm-1:00pm – Educational Presentation and Discussion

Registration Cost (Live or Remote): Free and open for all to attend.

Link will be emailed out the day PRIOR of the event. If you have not received the link, please email Kevin Gardner

Program Description: The clinical research landscape is constantly changing with ebbs and flows in amount of clinical trials being conducted in a given therapeutic area or indication. With this shifting landscape, how do clinical research sites put themselves in the best position for long term success? This webinar will break down therapeutic area trends over the years, what to expect for the rest of 2017 and beyond, as well as basic strategies for adapting in this ever changing landscape. Understanding the trends as well as strategies for adapting to changes in the clinical research industry, will help position sites for long term sustainable success.

Upon completion of this Webinar Replay, attendees should be able to:

• Understand therapeutic area trends in clinical research and their implications
• Learn what to expect in 2017 and beyond from a therapeutic area prospective
• Understand basic strategies for adapting to the changing clinical research landscape and putting clinical research sites in an optimal position for long term success

Contact hours: 1 Contact hours have been applied for through ACRP. Membership is not required for online registration of contact hours.

To receive contact hours: Purchase the contact hours, sign in at the registration desk, and attend the program. Log on to the ACRP website then “ACRP Learning Portal” to complete the evaluation no later than 30 days following the event and obtain the online certificate.

Contact Hour Cost:

• $0 Chapter Members
• $15 ACRP Members
• $30 Non-Members

Refund Policy: There are no refunds unless the program is cancelled by the chapter before the start of the program.

Level: Intermediate

Target Audience: Investigators, Clinical Research Staff and Administrators, Clinical Research Coordinators, Clinical Research Associates, Clinical Project Managers, Human Subject Protection Office personnel, Research Quality Assurance staff and anyone working in clinical research.

Further Information: CNEPA@acrpnet.org or Kevin Gardner kgardner@pennstatehealth.psu.edu