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Event Overview:

DIA is proud to present the 2017 Regulatory Submissions, Information, and Document Management Forum. This forum was initially three separate DIA meetings: EDM (Electronic Document Management), ERS (Electronic Regulatory Submissions), and RIM (Regulatory Information Management), each with their own unique histories. In 2015, those three meetings were combined into one forum in an effort to represent the end-to-end process of managing regulatory submissions and documents. The response to this approach has been incredibly positive with record attendance in 2016, as it serves as the premiere place for the discussion of emerging operational standards, best practices, and the processes for submission, creation, and maximum use of regulatory information. The forum continues to explore information generated along the drug development continuum life cycle and alignment to ever evolving regulatory and electronic standards.

The RIM Business focused track provides the opportunity to interact and share experiences related to processes for obtaining and managing regulatory information and the organizational impact, as well as gain a greater understanding of key issues shaping the global regulatory environment. The RIM Technology track will focus on standards related to submission of regulatory information, the tools necessary to effectively manage the information, and associated implementation experiences and lessons learned. The traditional ERS and EDM tracks will focus on emerging trends and best practices in regulatory submissions and electronic document management life cycle, respectively.

Featured topics

    Electronic Document Management
    Electronic Regulatory Submissions
    Regulatory Information Management for Businesses
    Regulatory Information Technical Management
    Identification of Medicinal Products (IDMP)
    Structured Authoring
    eTrial Master File

Exhibitor Information:

Reach Your Audience

At DIA conferences, medical product developers, regulators, academics, and patient advocates all come together in one place, eager to receive fresh insight and share new information. DIA conferences are the perfect place for you to communicate your key messages to an influential audience, efficiently and cost effectively.

The Regulatory Submissions, Information, and Document Management Forum offers interested companies a selection of exhibit and marketing opportunities.

About DIA:

For more than 50 years, DIA (the Drug Information Association) has served as a global forum for all those involved in health care product development and life cycle management to exchange knowledge and collaborate in a neutral setting. DIA is an essential resource that provides opportunities to extend debate and discussion to advance scientific and medical innovation.

If the DIA Regulatory Submissions, Information, and Document Management 2017 - Drug Information Association is important to your business, act now and make the appropriate connections. See the contact information below.

All information in Events In America is deemed to be accurate at the time we add it, and we take steps to verify all details and update our records when new information is provided, but as people, events and circumstances change, we caution users to independently confirm all information. and Events In America LLC make no guarantee of accuracy and assume no liability for inaccurate information.

Conference/Event Dates: 02/06/2017 - 02/07/2017
Classification: B2B
Primary Industry: Pharmaceutical
Other Industries: Associations, Health Information, Pharmaceutical, Professional Healthcare
Estimated Attendance: 500
Cost to Attend:
Audience: Professionals who are involved in:

Regulatory Affairs and Operations
Regulatory Information Management
Global Submission Managers/Project Managers
Medical, Technical, and Regulatory Writers
Data Managers
Information Technology and Support Personnel
Document and eRecords Managers
Essential Document Process and Business System Owners
Regulatory Standards Implementation Specialists and Associates
Clinical Operations Representatives
Quality Assurance and Compliance Professionals
Contract Researchers and Service Support Providers
Emerging Pharmaceutical/Biotech/Device Professionals
Vendor Relationship Managers
Venue: Bethesda North Marriott Hotel & Conference Center
Venue Phone: (301) 822-9200
Venue Type: Indoor - Convention Center
Official Conference Hotel:Bethesda North Marriott Hotel & Conference Center
Conference Hotel URL:
Number of Exhibitors:20+ (2016) (Previous Year)
Show Owner:Drug Information Association (DIA)
Show Manager:DIA
Sponsorship: Yes

Booth Size Booth Cost   Available Amenities
8' x 10' Standard $3,500   Electricity: Yes - Unknown Price
8' x 20' Standard Double $7,000 / Prices are subject to change.   Water: n/a
  Generator: n/a
  Marketing Vehicles Allowed: Call
Other Booth Sizes Available: n/a

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