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DIA’s Annual Canadian Meeting: Thinking Globally, Acting Locally for The Well-Being of the Patient

Oct 28 2014 8:00AM - Oct 29 2014 3:00PM | Ottawa Marriott Hotel 100 Kent Street Ottawa, ON K1P5R7 CANADA

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Pre-meeting Tutorials:  October 27, 2014
Risk Management Plans and Drug Utilization Studies in Canada
Non-Inferiority Trials – Design and Analysis Issues 

New communication platforms, technologies and the establishment of the “global village” have made the medicines’ life cycle rapidly evolving and increasingly global. Yet the fiduciary role of health care professionals and the life cycle management of the medicines by regulators, industry, and payers remains primarily a local responsibility. Information today is moving at the speed of light across borders, impacting each country differently due to varied regulatory and health care practices. This creates an obvious challenge for the government, industry, and health care providers in trying to find the best harmonized approaches. It represents an even greater challenge to patients and consumers in trying to make the best health care decisions. Therefore, the patient needs have to drive the improvements and changes in the regulatory environment and medicine development, commercialization and access. This requires transparent and appropriate communications so that patients and consumers can become well informed, educated, and empowered.

This year DIA will bring key thought leaders and experts from various fields to explore this challenging dilemma for the Canadian stakeholders. This meeting will address the following questions:

  • How can we remain among the top world innovators in the regulatory and health care science?
  • How can we harmonize with other regulatory jurisdictions and ensure sustainability of our regulatory and health care system?
  • How can we ensure the continuous access of quality and state-of-the art medicines and devices
  • How can we promote optimal health for Canadians?

Meeting Highlights

  • Keynote address
  • Multi-track breakout sessions
  • Pre-meeting tutorials
  • Call for abstracts
  • Networking reception
  • Tabletop exhibiting opportunities

Who Should Attend 

Professionals involved in:

  • Regulatory Affairs
  • Policy/Pharmacoeconomics
  • Clinical Development
  • Drug Safety/Pharmacovigilance
  • Patient Safety
  • Medical Communications
  • Quality Operations

Learning Objectives 

At the conclusion of this meeting, participants should be able to:

  • Describe the current and evolving regulatory environment in Canada
  • Recognize the challenges faced by various Canadian stakeholders in the development, regulation, harmonization, and the access of state-of-the-art medicines and devices within a global context
  • Discuss vendor management and the impacts of outsourcing
  • Describe the challenges around providing relevant and acceptable communications to patients, health care professionals and consumers

Special Offers 

Group Discount Available!
Register 3 and Get the 4th Free!

Hotel & Travel 

The conference will be held at the Ottawa Marriott Hotel. 
A limited number of rooms are available at the reduced rate shown below (DIA rate is guaranteed until Monday October 9, 2014, or until room block is filled). Please Note: In order to receive the reduced room rate, hotel reservations must be made through Travel Planners, and not directly with the hotel.  Contact information for Travel Planners is as follows: Attendees can follow this link or call +1.212.532.1660 or in the USA at 1.800.221.3531. When calling please select option 1 for “Hotel Reservations,” inform the phone agent that you are making a reservation for Event #14019. 

Standard Room Rate $153

Hotel Address: 100 Kent Street, Ottawa, Ontario K1P 5R7, Canada

Warning: Unauthorized Solicitation

The most convenient airport is Ottawa Macdonald-Cartier International Airport and attendees should make both airline and hotel reservations as early as possible.

Contact Information 

Printable Registration Form

Registration Questions
Customer Service Department
Toll Free: 1.888.257.6457
Phone: +1.215.442.6100
Fax: +1.215.442.6199

Agenda Details
Rachel Minnick, Content Lead
Phone +1.215.442.6131
Fax +1.215.442.6199

Jessica McGrory, In-company Training Manager
Phone +1.215.442.6182
Fax +1.215.442.6199


Event Logistics
Stephanie Ritter, Event Planner
Phone +1.215.442. 6149
Fax +1.215.442.6199

Tabletop Exhibit Information
Jeff Korn, Exhibits Associate
Phone +1.215.442.6184
Fax +1.215.442.6199

Continuing Education 

DIA is accredited by the Accreditation Council for Pharmacy Education as a provider of continuing pharmacy education. DIA designates this educational activity for up to 9 contact hours or 0.9 continuing education units (CEUs).
Type of Activity: Knowledge

ACPE Credit Request – UPDATE
DIA is required by the Accreditation Council for Pharmacy Education (ACPE) to report pharmacy-requested CEUs through the CPE Monitor system. All ACPE-certified activity credit requests need to be submitted through DIA’s My Transcript within 45-days post activity. Pharmacists will need to provide their National Association of Boards of Pharmacy (NABP) e-Profile ID and date of birth (MMDD) to ensure the data is submitted to the ACPE and NABP properly. If you need to obtain your NABP e-Profile, please visit www.cpemonitor.net.

DIA has been accredited as an Authorized Provider by the International Association for Continuing Education and Training (IACET).

As an IACET Authorized Provider, DIA offers CEUs for its programs that qualify under the ANSI/IACET Standard. DIA is authorized by IACET to offer 1.1 CEUs for the meeting and .3 for each tutorial. Participants must attend the entire program in order to be able to receive an IACET statement of credit. No partial credit will be awarded.

DIA’s Certificate Program Statement
This program is part of DIA’s Certificate Program and is awarded the following:
• Clinical Research Certificate Program: 7 Elective Units • Clinical Safety and Pharmacovigilance Certificate Program: 4 Elective Units
• Project Management Certificate Program: 8 Elective Units • Regulatory Affairs Certificate Program: 7 Elective Units

For more information go to www.diahome.org/certificateprograms

Name Credit Type Max Credits CEU
DIA’s Annual Canadian Meeting ACPE 9.00 0.900
DIA’s Annual Canadian Meeting IACET 10.75 1.100

Disclosure Policy:

It is DIA policy that anyone in a position to control the content of a continuing education activity must disclose to the program audience (1) any real or apparent conflict(s) of interest related to the content of their presentation and/or the educational activity, and (2) discussions of unlabeled or unapproved uses of drugs or medical devices. Disclosure statements will be included in the course materials.

Statement of Credit:

If you would like to receive a statement of credit, you must attend the meeting (and tutorial, if applicable), sign in at the DIA registration desk each day, and complete the on line credit request process through My Transcript. To access My Transcript, please go to www.diahome.org, select “Login to My DIA” and you will be prompted for your user ID and password. Select “My Transcript” (left side bar) and “Credit Request” to process your credit request. Participants will be able to download a statement of credit upon successful submission of the credit request. My Transcript will be available for credit requests on Wednesday, November 12, 2014.

To view DIA’s grievance policy, please visit the CE page on the DIA website at www.diahome.org/CE

Program Committee 

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Tutorials Monday, Oct 27, 2014

  • 1:30PM - 5:00PM

    Risk Management Plans and Drug Utilization Studies in Canada

Day 1 Tuesday, Oct 28, 2014

  • 10:30AM - 12:00PM

    Plenary Session 2: Putting Patients First; What Does It Look Like in 2014 to be a Patient-Centric Organization - Part 2

    Session Chair(s):

    • Marie-Ange Noue, PhD
      Proj. Manager, Drug Safety/Medical Information, Deputy Local Drug Safety Officer
      EMD Serono, Canada

    Part 2 of this plenary session will focus on the health care, patient organization and payer perspective of being a patient-centric organization.


    • Uncoordinated Ethical Insights about Patient Participation
      Bernard Keating, PhD
      Prof, Dir, Applied Ethics Programs, Faculty of Theology and Religious Studies
      Laval University, Canada
    • Partnering with Patients in Healthcare Decision Making
      Durhane Wong-Rieger, PhD, MA
      President and Chief Executive Officer
      Canadian Organization For Rare Disorders (CORD), Canada
    • Patient Input and Evidence-Bringing Life to HTA
      Chander Sehgal, MD, MBA
      Director, CDR and Rapid Response
      CADTH, Canada
  • 12:00PM - 1:30PM

  • 1:30PM - 3:00PM

    Session 3 - Track A: Communications with Regulators and Among Industry

    Session Chair(s):

    • Vratislav Hadrava, MD, PhD
      Vice President and Medical Director, Global Innovative Products
      Pfizer Canada, Inc., Canada

    Good communication between industry and regulators is a cornerstone of predictable process and outcome in review and regulatory decision making of all regulatory files as well as in consultation on new or updating regulations, guidances and policies. The session will primarily provide overview of key principles and challenges during the first cycle review in Canada and US with reflection on possible evolution and improvements. It will be complemented by learnings from Health Canada effective risk communication needs, planning and process.


    • Agency and Industry Perspectives on FDA Regulatory Review Transparency and Communication
      Jayne C. Ware, MPH, MS
      Director, Global Regulatory Policy
      Merck & Co., Inc., United States
    • Communications with Regulators and within Industry
      Loretta Del Bosco
      Director, RA & QA Operations
      AbbVie Corporation, Canada
    • Risk Management Planning in Canada
      Matthew Bown
      Associate Director, Marketed Health Products Directorate
      Health Canada, Canada
  • 1:30PM - 3:00PM

    Session 3 - Track B: Vendor Management

    Session Chair(s):

    • Carolyne Desrosiers
      Manager, Regulatory Projects
      Lundbeck Canada Inc, Canada

    Suppliers and 3rd parties play a key role in today’s pharmaceutical industry. Outsourced activities such as clinical trial management, manufacturing, analysis, warehousing, and distribution are commonplace. Vendor management is an important discipline that enables organizations to control costs, drive service excellence and mitigate risks to gain increased value from their vendors throughout a project’s life cycle.


    • From the Vertical to Horizontal Integration: Benefits and Pitfalls of Outsourcing Manufacturing
      Mohammed Razdar Khan
      Synergex Consulting, Canada
    • Vendor Oversight for Small and Medium Sized Sponsors: Methods to Achieve Operational, Compliance, and Business Objectives
      Peter Motteram, MSc
      P.A.S.M. Limited, United Kingdom
    • Vendors in Clinical Development
      Loubaba Cherkaoui, MSc
      Pharma GCP Auditor, Global Development Quality Assurance Audit Expert
      Novartis Pharmaceuticals Canada Inc., Canada
  • 1:30PM - 3:00PM

    Session 3 - Track C: Patient Access

    Session Chair(s):

    • Marie-Ange Noue, PhD
      Proj. Manager, Drug Safety/Medical Information, Deputy Local Drug Safety Officer
      EMD Serono, Canada

    The research-based pharmaceutical industry is driven to produce innovative medicines that will benefit patients. However, regulatory approval of a drug for sale in Canada does not necessarily mean that provincial and territorial governments will fund it. Therefore while ensuring prompt and equitable patient access to innovative medicines is a major concern to key stakeholders, the Canadian pharmaceutical and biotechnology industry is faced with the challenge of having to reconcile the needs of patients to have access to important new treatments, the requirement of the payer to manage scarce resources, and the constraints of the companies that discover these innovations. This session will look at the broad spectrum of the drug approval process from the regulatory, payer (specifically how evidence-based information influences decision makers) and industry perspectives. From the review of new drug submissions to provincial/territorial decision for product listing and everything in between, each of the speakers will discuss their role in making inroads to improve and facilitate access to medicines including non traditional/accelerated pathways, investigational access, and trends in orphan drugs/rare diseases.

    Speakers will address this important topic: How can we ensure the continuous access of patients to quality and state-of-the art medicines?


    • Access to Drug Therapies - Health Canada's Role, Initiatives and Challenges
      John Patrick Stewart, MD
      Executive Medical Director of Therapeutic Products Directorate
      Health Canada, Canada
    • Pan-Canadian Approach for Public Drug Program Funding Recommendations
      Brent Fraser
      Director, Drug Program Services, OPDP
      Ontario Ministry of Health, Canada
    • Achieving Market Access Success - A Manufacturer's Perspective
      Lindy Forte
      Principal Consultant
      Patient Access Solutions, Canada
  • 3:00PM - 3:30PM

    Refreshment Break
  • 3:30PM - 5:00PM

    Session 4 - Track A: Unique Regulatory Requirements in Canada

    Session Chair(s):

    • Rocelyn DelCarmen
      Director, Regulatory Affairs and Quality Assurance
      AstraZeneca, Inc., Canada

    Harmonization efforts have streamlined many regulatory requirements across the globe. There remains a few areas in the regulatory regime where Canadian requirements differ from other regions. During this session Health Canada and Industry speakers will review these areas of differentiation with a discussion of why the regime exists, and how stakeholders “act locally” to address it.


    • Impact of Canadian Specific Requirements for CRFs
      Samar Darwish, MSc
      Director, Regulatory Affairs and Drug Safety
      Boehringer Ingelheim Canada, Canada
    • Health Canada Regulations –The Nuts and Bolts: Importation & Release of Drug Products
      David Lessard
      Director of Quality and Compliance
      Pfizer Canada Inc., Canada
    • Bioequivalence – Health Canada’s Perspective
      Paul Wielowieyski
      Acting Manager, Division of Biopharmaceutics Evaluation
      Health Canada, Canada
  • 3:30PM - 5:00PM

    Session 4 - Track B: Inspectorate Town Hall – GVP Inspections

    Session Chair(s):

    • Chanez-Narimene Kebache
      Manager, Pharmacovigilance
      Mallinckrodt Pharmaceutical, Canada

    As part of Health Canada’s (HC) mandate to maximize the safety, quality and efficacy of health products, the Health Product and Food Branch (HPFB) Inspectorate posted in 2013 on the HC’s website the new guidance document entitled “Good Pharmacovigilance Practices (GVP) Guidelines” (GUI-0102) and the revision to the “Risk Classification of Good Pharmacovigilance Practices (GVP) Observations” (GUI-0063).

    The industry’s perspective on the impact of the implementation of GUI-0102 and GUI-0063 on the conduct of GVP inspections will be discussed with an opportunity for interactive participation by the audience. A HC’s Inspectorate representative will provide an overview of the main deficiencies observed during GVP inspections that have been conducted since the implementation of GUI-0102.


    • GVP Inspections: Information Update on the Implementation of the Good Pharmacovigilance Practices (GVP) Guidelines (GUI-0102)
      Sophie Lafrance
      Compliance Officer, HPFB Inspectorate
      Health Canada, Canada
    • Inspectorate Town Hall –Good Pharmacovigilance Practices (GVP) Inspections
      Agnes Jankowicz
      Executive Director, PV
      Certus PV Services Inc., Canada
    • Robert Milne, RAC
      Manager Drug Safety / Medical Information
      EMD Serono, Canada
  • 3:30PM - 5:00PM

    Session 4 - Track C: Communication to Patients and Public/Consumer

    Session Chair(s):

    • Janice Lobo-Dale
      Regulatory Analyst, Biologics and Genetic Therapies Directorate
      Health Canada, Canada

    With a focus on transparency and openness for increased health benefits and mitigated health risks, regulatory agencies in consultation with drug manufacturers and in collaboration with other key stakeholders and partners are strengthening the approach taken to communicate with patients and consumers. This session will focus on initiatives taken by government agencies and drug manufacturers to make available drug product information in plain language. The concept of available, clear, comprehensive and useful information related to authorized medicines is guiding the strategies for improved guidance, new regulations and increased communication to patients/consumers.


    • Health Product Register
      Denis Mulhall
      Executive Director, Information Management and Technology (HPFB)
      Health Canada, Canada
    • How Patients and Public View Regulator Communication
      Durhane Wong-Rieger, PhD, MA
      President and Chief Executive Officer
      Canadian Organization For Rare Disorders (CORD), Canada
    • Recent FDA Activities Related to Communicating Medication Information to Consumers
      Jayne C. Ware, MPH, MS
      Director, Global Regulatory Policy
      Merck & Co., Inc., United States

Day 2 Wednesday, Oct 29, 2014

  • 7:30AM - 8:30AM

    Continental Breakfast
  • 8:30AM - 10:00AM

    Session 5 - Track A: Transforming Drug Safety and Surveillance

    Session Chair(s):

    • Rocelyn DelCarmen
      Director, Regulatory Affairs and Quality Assurance
      AstraZeneca, Inc., Canada

    In 2014, the Government of Canada introduced Bill C17 and many provisions included in the bill will assist in transforming drug safety and surveillance. During this session Health Canada and Industry will provide insight into how drug safety and surveillance will change in the future as new laws and systems are put into place in Canada.


    • Continuous Improvement Efforts by Health Canada to Enhance the Human Cells, Tissues and Organs Surveillance System in Canada
      Melanie Cassandre Derry, MD
      Scientific Evaluator
      Health Canada, Canada
    • Implementing C17, Update and Next Steps-Health Canada Perspective
      David K. Lee
      Director, Office of Legislative and Regulatory Modernization, HPFB
      Health Canada, Canada
    • Implementing C17 Opportunities and Challenges - Industry Perspective
      Keith McIntosh
      Senior Director, Scientific & Regulatory Affairs
      Rx & D, Canada
  • 8:30AM - 10:00AM

    Session 5 - Track B: New Technologies and Evolving Science as a Challenge to Regulatory Framework

    Session Chair(s):

    • Matthew Ryan
      Senior Advisor, Director General's Office, Therapeutic Products's Directorate
      Health Canada, Canada

    New technologies and evolving science are critical to the advancement of health care and treatment options for patients. Researchers, academia and the pharmaceutical industry have all played a significant role in bringing new drug and medical device technologies to market, leading to increased health benefits for Canadian patients. Even moreso today, scientific and technological advancements are being developed at a rapid pace, requiring effective support in order to advance from discovery, through development and into commercialization. Some of these advancements fit well into existing regulatory frameworks, while others present challenges and even potential barriers to what is needed in today’s environment. The regulator is also faced with challenges in using existing regulations in the application of science and technological advancements that could not have been foreseen even a few years. Speakers will present on these new challenges and how they are being addressed under today’s regulatory environment and how we need to re-think our approaches to these scientific and technical opportunities. While there are challenges, there are also opportunities for all areas of the pharmaceutical spectrum, including from both Industry and governments, to play a leadership role in facilitating science and regulation in the development of safe and effective drug therapies.


    • Overview of Health Canada's Initiatives in Tamper-Resistance and Abuse Deterrence
      Kimby N. Barton, MSc
      Director of Bureau of Cardiology, Allergy and Neurological Sciences
      Health Canada, Canada
    • New Technologies and Evolving Science as an Opportunity for the Regulatory Framework
      Barbara E. Tardiff, MD, MBA
      Vice President, Development Operations
      Pfizer Inc., United States
    • Overview of Canadian Guidance Documents on Rare Diseases
      Agnes V. Klein, DrPH, MD
      Director, Evaluation of Radiopharmaceuticals and Biotherapeutic Products
      Health Canada, Canada
  • 8:30AM - 10:00AM

    Session 5 - Track C: Health Technology Assessments

    Session Chair(s):

    • Karen Feltmate
      Redstone Health Group, Inc., Canada

    While regulators have developed avenues to provide patients early access to new therapies ie priority review, NoC with conditions, it is not as obvious what the post NoC market Access Stakeholders ie Drug Programs, Public and Private have/are doing. This session will look at various Market Access Stakeholders, their role in the Market Access process, their responsibility to patients within their jurisdiction and how their HTA review aligns to their patient responsibility.


    • Private Payer HTA Assessor Perspective
      Thomas Holloway
      Equitus Consulting Inc., Canada
    • Patient Perspectives on the Impact of HTA on Patient Access to Medicines
      Wayne Critchley
      Senior Associate, Health & LIfe Sciences
      Global Public Affairs, Canada
    • Chander Sehgal, MD, MBA
      Director, CDR and Rapid Response
      CADTH, Canada
  • 10:00AM - 10:30AM

    Refreshment Break
  • 10:30AM - 12:00PM

    Session 6 - Track A: Subsequent Entry Biologics/Biosimilars

    Session Chair(s):

    • Andrew Storey
      Vice President, Regulatory Affairs United States and Canada
      AbbVie, United States

    With the expiration of numerous patents for originator biologicals and the development of follow-on products, the market for biosimilars is growing at a rapid pace. These biosimilars and follow-on biologics have garnered interest for their cost-effective benefits in patient care but questions remain about many aspects of “similarity." As biosimilars become more available to patients, there are important factors for patients and health care providers that must be addressed. This session will focus on the innovations, technologies, and regulatory information surrounding biosimilars

    Topics to be covered include Canadian and US Regulatory Developments, Interchangeability, Labeling, Naming, and Extrapolation and will be reviewed from various perspectives.


    • Biosimilars in Canada: Does the Process Differ From Other Countries?
      Agnes V. Klein, DrPH, MD
      Director, Evaluation of Radiopharmaceuticals and Biotherapeutic Products
      Health Canada, Canada
    • Extrapolation, Naming and Consistency
      Keith Watson, PhD
      AbbVie Ltd, United Kingdom
    • Navigating the Marketing Application Process for Subsequent Entry Biologics
      Allison Guy, MSc, RAC
      PAREXEL International, Canada
    • Navigating the Marketing Application Process for Subsequent Entry Biologics
      Christopher Shanne
      Sr. Consultant
      PAREXEL International, United States
    • Common Drug Review Process for Reviewing Subsequent Entry Biologics
      Brendan McIntosh
      CADTH, Canada
  • 10:30AM - 12:00PM

    Session 6 - Track B: Biostatistics

    Session Chair(s):

    • Deirdre Cozier
      Senior Manager, Regulatory Affairs (Canada)
      Pendopharm, Division of Pharmascience, Canada

    The session’s objectives is to present the challenges of using the statistics from the drug development plan across the lifecycle of the product. Clinical development plans are geared towards product approval in a given region and are based on the health authorities’ requirements and international standards. In Canada, these statistical measures will be used to demonstrate the benefit of the drug to various decision-makers at the national and provincial level and also with prescribers. In large multinational companies these data may (or may not) fit the needs of the Canadian environment in the pre-market and post-market phase. The speakers will include a Health Canada perspective on evaluating statistical evidence generated at an international level to a Canadian context, an industry talk on interfacing with the various stakeholders to ensure alignment of need for informed decision-making, and from an advertising review agency on how best to use the stats you have to communicate the benefits of the drug to a healthcare professional.


    • Using the Stats You Have to Communicate Drug Benefts to HCPs (with an emphasis on RCTs)
      Patrick Massad
      Chief Review Officer
      Pharmaceutical Advertising Advisory Board (PAAB), Canada
    • Evaluating Statistical Evidence Generated at an International Level: A Regulatory Perspective
      Catherine Njue, PhD
      Bisostatistics Advisor - Clinical Trials, CERB
      Health Canada (BGTD), Canada
    • Global Development Plans: Adaptation and Challenges for Canada
      John A. Stewart, MSc
      Manager, Biostatistics
      Sanofi-Aventis Canada, Canada
  • 10:30AM - 12:00PM

    Session 6 - Track C: Simplifying Clinical Trial Execution in Canada in the Interest of Patients

    Session Chair(s):

    • Janice Lobo-Dale
      Regulatory Analyst, Biologics and Genetic Therapies Directorate
      Health Canada, Canada

    Session 6 - Track C: Simplifying Clinical Trial Execution in Canada in the Interest of Patients


    • Best Practices for Managing Succesful Clinical & Pharmaceutical Projects
      Zizi Imatorbhebhe, MBA, MS, PMP
      Principal & Managing Consultant
      Alliance Bio-Pharm & Health Partners, United States
    • Clinical Trials in Canada: Extraterritorial Application of US Laws and Regulations
      Jack Corman
      Canadian Association For Independent Clinical Research, Canada
    • The Initiative to Streamline Investigator Initiated Clinical Trials: Guidelines for Managing Canadian Regulatory Expectations
      Karen Arts, BSN, MSN, RN
      Director, Business Development, High Impact Clinical Trials
      Ontario Institute For Cancer Research, Canada
  • 12:00PM - 1:30PM

  • 1:30PM - 3:00PM

    Plenary Session 7 - Evolving the Healthcare and the Therapeutic Options by Putting Patients First

    Session Chair(s):

    • Vratislav Hadrava, MD, PhD
      Vice President and Medical Director, Global Innovative Products
      Pfizer Canada, Inc., Canada
    • Co Pham
      Senior Scientific Advisor, Marketed Health Products Directorate
      Health Canada, Canada

    Plenary Session 7 - Evolving the Healthcare and the Therapeutic Options by Putting Patients First


    • Patient Perspective
      Maureen Smith
      Patient Advocate / Secretary
      Canadian Organization For Rare Disorders (CORD), Canada
    • Evolving Healthcare and Therapeutic Options by Putting Patients First
      Roland Halil
      Assistant Professor, Department of Family Medicine
      University of Ottawa, Canada
    • Kelvin Kenneth Ogilvie
      Senator, Chair-Senate Standing Committee Social Affairs, Science and Technology
      Parliament of Canada, Canada


The Annual Canadian Meeting offers interested companies the opportunity to exhibit with a tabletop display.

Tabletop Fee: $1,500

Fee Includes:

  • One six-foot skirted table
  • One chair
  • Standard electricity

Each tabletop rental requires at least one registered attendee to staff the table. All tabletop staff must be registered conference attendees.

Tabletop Exhibit Dates: October 28-29, 2014

Useful Links:

  • Contact Canada
  • DIA
  • LORENZ Life Sciences Group
  • Optum

Registration Fees 


Member Government
Member Academia
Member Standard


NonMember Government
NonMember Academia
NonMember Standard
Group Discounts\Registration

Printable Registration Form

Group Discount

Register three individuals from the same company and receive complimentary registration for a fourth! All four individuals must register and prepay at the same time – no exceptions.

To take advantage of this offer, please make a copy of the registration form for EACH of the four registrants and include the names of all other group registrants in the Group Discount section. DIA will apply the value of the lowest applicable fee to this complimentary registration; it does NOT include fees for optional events or DIA membership. You may substitute group participants of the same membership status at any time; however, administrative fees may be incurred.

Group registration is not available online and does not apply to the already-discounted fees for government or charitable nonprofit/academia.

Register Online

Unless otherwise disclosed, the statements made by speakers represent their own opinions and not necessarily those of the organization they represent, or that of the Drug Information Association. Speakers, agenda and CE information are subject to change without notice. Recording of any DIA educational material in any type of media is prohibited without prior written consent from DIA.

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