Amarex Clinical Research

Managing Clinical Trials with Speed and Precision

Calendar

Seminars and Workshops

Amarex conducts seminars and workshops that provide information on, and training in, many aspects of clinical research.

SCHEDULED  EVENTS:

Meeting the FDA Requirements for a Clinical Trial: Investigator, Staff and IRB Responsibilities

Workshop to be conducted October 13th at NIH campus by Mukesh Kumar, PhD, RAC , Senior Director of Regulatory Affairs and Quality Assurance, Amarex Clinical Research.

Bldg 10; 11S235 - Wolfe Conference Room
Contact Info: 301-435-6243 or 301-594-3734 or goldbar@mail.nih.gov

Go to: http://calendar.nih.gov/app/MCalWelcome.aspx and select day Oct 13th.

For your convenience, a copy of the workshop slides have been provided here.

UPCOMING EVENTS:

  • Challenges and opportunities for Outsourcing Clinical Product Development to India
  • Exploratory INDs: The use of Phase 0 Studies in Clinical Development Planning
  • HIPAA Privacy Rule and Clinical Research, Certification Class
  • Preparing for an FDA GCP or GLP Compliance Audit
  • The Interim Analysis - when and how
  • Informed Consent Form Development
  • Statistical Analysis Plans Made Easy
  • Clinical Site Coordinator Training and Certification
  • How to Become a Clinical Site

CONFERENCE EXHIBITS: Amarex has exhibited at or plans to participate in the annual meetings of the following organizations: