Atlantic City, New Jersey

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Date(s) - September 21,2019 - September 22,2019
8:00 am - 1:00 pm

Harrah's Atlantic City


HOTEL  INFO:  please call us to assist with your reservation SUNDAY IS SOLD OUT
Harrah’s Resort Atlantic City Friday $119, Saturday $199 single or double occupancy. Extra adult in room $20 per night.

Dr. Renee Jones, Pharm D.

Nova Southeastern University

Renee Greaves currently serves as the Director of Preceptor Development as Assistant Professor at Nova Southeastern University in Ft. Lauderdale, Florida. She has served as the Pharmacy Operations Supervisor and Residency Coordinator of Broward Health, where she implemented clinical pharmacy programs such as HIV and antibiotic stewardships, hepatic monitoring, cardiopulmonary discharge counseling, and internal medicine clinical rounds with graduate medical education residents. She has also served as a Clinical Assistant Professor of Rutgers University School of Pharmacy where she taught didactic courses such as Infectious Disease Therapeutics and numerous electives.

Saturday September 21,2019


ACPE # 0043-9999-19-026-L01-P


1.  Discuss the clinical indications for the new medications approved by the FDA.

2. Explain the various mechanisms of action for the medications discussed within this program.

3.  Recognize the clinically relevant drug interactions for the medications.

4.  Identify the most common adverse reactions for the new drug approvals.

5.  Explain the approved dosing guidelines and recommended dosage adjustments for the medications reviewed.


Dr. Martha M. Rumore, Pharm D., JD, MS, LLM, FAPhA

Of Counsel Sorell, Lenna & Schmidt, LLP & Adjunct Professor, Maurice A. Deane School of Law at Hofstra University

Dr. Martha Rumore is a pharmacist/attorney admitted to the NY, NJ, and DC bars. She has a Pharm D. from St. John’s University, a MS in Drug Information from Long Island University, a JD from CUNY School of Law, and an LLM in Intellectual Property from the Benjamin N. Cardozo School of Law. She is currently Of Counsel at the law firm of Sorell, Lenna & Schmidt, LLP in New York and a Clinical Pharmacist at Montefiore Medical Center in New York. At the law firm she focuses on pharmaceutical and medical device intellectual property including all aspects of patent law prosecution and transactional matters. She has over 15 years of law firm experience in the area of pharmaceutical intellectual property, especially generic pharmaceuticals. She has also worked in the pharmaceutical industry and hospital pharmacy, both at the Director level. She taught Pharmacy Law at both Long Island University and Touro College of Pharmacy for close to 20 years. In 2017, she won the Touro Faculty Research and Scholarship Award. Martha is a frequent lecturer and has over 200 publications and presentations. She is a Fellow and former Trustee of the American Pharmacists Association and in 2015 received the APhA-APPM Poster Merit Award. She is also a former member of the American Society for Pharmacy Law Board of Directors and received the 2015 Larry Simonsmeier Legal Writing Award.

Sunday September 22, 2019


ACPE # 0043-9999-19-038-L03-P and 0043-9999-19-039-L05-P


1.  Examine recent legislative, legal, and regulatory changes impacting pharmacists on the state and federal level.

2.  Describe recent court cases that are relevant to pharmacy practice and how those cases may affect the attendee’s behavior in providing pharmacy services.

3.  Understand pharmacy federal and state laws, regulations and the role of the state boards of pharmacy.

4.  Identify the resources available in addressing and evaluating issues pertaining to controlled substances in both community and institutional pharmacy practice.

5.  Describe how medication errors and adverse drug events in prescribing, dispensing, administration and patient education can be prevented.

6.  Understand the extent and effect of medication errors on patient health and safety.

7.  Evaluate opportunities and challenges for postmarketing surveillance and adverse drug reaction notification and reporting.

8.  Identify best practices to decrease potential liability from medication errors.


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