Brandy Chittester, Director of Clinical Monitoring and Mary Lewis, Chief of Clinical Operations for IMARC Research will both be speaking at MAGI's Clinical Research Conference in Philadelphia, May 4-7, 2014. I hope you can join us and over 500 others.
Brandy will discuss “Site Monitoring with an Auditor's Eye,” while Mary’s presentation will focus on “Challenges in Conducting Medical Device Trials.” Here is a full listing of speakers at the conference.
MAGI conferences feature a coherent program emphasizing practical tips based on real-life examples, with lots of interaction and networking. This conference will feature:
- 200+ speakers.
- 90+ sessions and workshops in seven tracks: site operations, sponsor operations, regulatory & ethics, contracts, budgets & billing, quality, and special topics.
- 22+ continuing education contact hours: CME, CNE, CLE, CCB, ACRP (CCRA, CCRP, CCTI, CPI), CCIP (CIP), HCCA (CCB), NAIM (CIM), PMI (PMP, PgPM), PMI (CMOM), PRIM&R (CIP), RACC (RAC), SoCRA (CCRP), and SQA (RQAP).
- Excellent networking: Two-thirds of attendees will have 5+ years of experience. About 50% of attendees will be from sites, 20% from sponsors, 10% from CROs, and 20% from others.
MAGI’s mission is to standardize best practices for clinical research operations, business and regulatory compliance. ("MAGI" stands for Model Agreements and Guidelines International. It is pronounced with "G" as in Georgia and "I" as in Ireland.) MAGI's 9,000+ members represent most of the major players in the industry. Membership is free.
IMARC assists the clinical research community in the pursuit of FDA and worldwide approvals. IMARC is committed to being an industry thought leader and both Brandy and Mary hope to see everyone at the MAGI Conference.
See you in Philadelphia!
Photo Credit: dolescum