AUGUST 8-10, 2018
FDAnews — ICH E6 GCP Interactive Workshop
Waltham, MA

SEPTEMBER 10-12, 2018
Mastering EU Medical Device Regulation
Philadelphia, PA

JULY 1-31, 2018
Program Phlebotomy Training — Two Day Training
Various locations

JUNE 21, 2018
The Real Impact of Common Rule in 2018: Understanding Nuances, Facilitating Compliance & Implementing Best Practices
Fully understand the key changes to the Common Rule and how they dramatically impact IRBs and virtually every entity engaged in clinical research. Changes to Informed Consent and Broad Consent, the Implementation of Limited IRB Review and much more.

JULY 11, 2018
Preparing for the MDSAP Audit Process: A Case Study from the Manufacturer’s Perspective
Consultant Connie Hoy takes you through the changes — what’s the same, what’s different about the audit and inspection process as the new Medical Device Single Audit Program (MSDAP).