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Meetings & Training

DIA’s comprehensive educational portfolio reflects and advances innovation in the pharmaceutical, biotechnology, medical device, and related fields and facilitates open dialogue among key professionals from industry, government, academia, and patient organizations.

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Name Start Date Credits Format Region Location
Clinical Investigator: Module 2 - Conducting The Study Jul 26, 2014 ACPE, CME Online Instruction North America Online
Clinical Investigator: Module 1 - Study Preparation and Initiation Jul 26, 2014 ACPE, CME Online Instruction North America Online
Informed Consent Jul 26, 2014 ACPE Online Instruction North America Online
Crisis Management Jul 26, 2014 ACPE, IACET Online Instruction North America Online
Database Management Jul 26, 2014 ACPE, IACET Online Instruction North America Online
Literature Evaluation Jul 26, 2014 ACPE, IACET Online Instruction North America Online
Literature Searching Jul 26, 2014 ACPE, IACET Online Instruction North America Online
Medical Inquiries Jul 26, 2014 ACPE, IACET Online Instruction North America Online
Medical Writing Jul 26, 2014 IACET Online Instruction North America Online
Product Labeling Jul 26, 2014 ACPE, IACET Online Instruction North America Online
Regulatory Issues Jul 26, 2014 ACPE, IACET Online Instruction North America Online
Statistics for Medical Communications Professionals Jul 26, 2014 ACPE, IACET Online Instruction North America Online
The Use of Mobile Medical Applications as Companions Jul 26, 2014 Online Instruction Global Online
Regulating a Social World Jul 26, 2014 Online Instruction Global Online
Generic Drug Labeling Proposed Rule and Safety Updates Jul 26, 2014 Online Instruction Global Online
English Literacy and Spanish Transcreation of Patient Documents: Concepts for Low Literacy Materials Jul 26, 2014 Online Instruction Global Online
Big Data: Impact of Health Care Reform on Collaborations and Strategies Jul 26, 2014 Online Instruction Global Online
Implementation of the FDASIA Patient Provisions Jul 26, 2014 Online Instruction Global Online
Complimentary: Regulatory and Real World Evidence Challenges of Rare Diseases and Orphan Drugs Jul 26, 2014 Online Instruction Global Online
Variations in the European Union: CMC/Quality Changes Jul 26, 2014 Online Instruction Global Online
Good Pharmacovigilance Practice: How Good has it Proven to be for Industry? Jul 26, 2014 Online Instruction Global Online
Safety and Social Media: Is this the Question or the Answer Jul 26, 2014 Online Instruction Global Online
Pharmacovigilance and Risk Management: Patient Perspective Jul 26, 2014 Online Instruction Global Online
Complimentary Patient-Centeredness and Engagement in Clinical Research: Opportunities for Industry Jul 26, 2014 Online Instruction Global Online
Drug Safety Regulatory Requirements Jul 26, 2014 ACPE, IACET Online Instruction Global Online
Premarketing Clinical Trial Safety Jul 26, 2014 ACPE, IACET Online Instruction Global Online
Postmarketing Safety Management Jul 26, 2014 Online Instruction Global Online
Basics of Signal Detection and Pharmacoepidemiology Jul 26, 2014 Online Instruction Global Online
Safety Audits and Inspections Jul 26, 2014 Online Instruction Global Online
Five-Part Series on Fundamentals of Clinical Pharmacology for Drug Development - Part 1: Fundamentals of Clinical Pharmacology: Pharmacokinetics Jul 26, 2014 Online Instruction Global Online
Designed for Success: Utilizing Protocol Quality by Design (QbD) to Plan Clinical Studies Jul 26, 2014 Online Instruction Global Online
Negotiation and Influence Jul 26, 2014 Online Instruction Global Online
China Update: Regulatory Changes and Implications Jul 26, 2014 Online Instruction Global Online
Evaluation and Management of Cardiac Conditions in Oncology Patients Jul 26, 2014 Online Instruction Global Online
Risk Management of Medicinal Products: REMS and RMP - Need for Harmonization Within the ICH Region? Jul 26, 2014 Online Instruction Global Online
Introduction to Drug Safety Jul 26, 2014 ACPE, IACET Online Instruction Global Online
How to Prepare for a Safety Inspection Jul 26, 2014 Online Instruction Global Online
CDER Town Meeting: Safety Hot Topics Jul 26, 2014 Online Instruction Global Online
Assessing the Benefits and Risks of Medicines: Webinar Series - Part 1: Introduction to the Benefit-Risk - Why is Everyone Talking about Benefit-Risk? Jul 26, 2014 Online Instruction Global Online
Assessing the Benefits and Risks of Medicines: Webinar Series Part 2 - Benefit-Risk Assessment a Changing Regulatory Landscape Jul 26, 2014 Online Instruction Global Online
Assessing the Benefits and Risks of Medicines: Webinar Series - Part 3: Framing for Benefit-Risk Assessment and Communication Jul 26, 2014 Online Instruction Global Online
Assessing the Benefits and Risks of Medicines: Webinar Series - Part 4: Clinical Judgment and Pragmatic Considerations for Endpoint Selection and Display in Benefit-Risk Jul 26, 2014 Online Instruction Global Online
Assessing the Benefits and Risks of Medicines: Webinar Series- Part 5: Stated Choice Methods for Valuing Benefits and Risks Jul 26, 2014 Online Instruction Global Online
Assessing the Benefits and Risks of Medicines: Webinar Series-Part 6: Multi-criteria Decision Analysis to Assist in the Decision Making Process Jul 26, 2014 Online Instruction Global Online
Assessing the Benefits and Risks of Medicines: Webinar Series- Part 7: A Structured, Quantitative Health Outcomes Approach to Drug Benefit-Risk Analysis Jul 26, 2014 Online Instruction Global Online
Assessing the Benefits and Risks of Medicines: Webinar Series- Part 8: Visualization and Communication of Benefit-Risk Jul 26, 2014 Online Instruction Global Online
New Good Pharmacovigilance Practice (GVP) Documents in Canada Jul 26, 2014 Online Instruction Global Online
Clinical Statistics for Nonstatisticians Jul 26, 2014 Online Instruction Global Online
Development of a Clinical Study Report Jul 26, 2014 Online Instruction Global Online
Complimentary Biomarker Strategies for More Efficient Early-Phase Drug Development in Alzheimer's Disease Jul 26, 2014 Online Instruction Global Online
CardioVascular Safety: The New Paradigm - Proarrhythmic Assessment of New Drugs without the Thorough QT Study Jul 26, 2014 Online Instruction Global Online
CardioVascular Safety – What are the Key Issues Regarding Blood Pressure Assessment During Clinical Development Jul 26, 2014 Online Instruction Global Online
Introductory Principles and Application of Risk Management within Clinical Operations Jul 26, 2014 Online Instruction Global Online
Electronic Submissions 101 – Essential MS Word and Adobe Acrobat Tools/Skills and Current IT Options Jul 26, 2014 Online Instruction Global Online
A Tour of FDA Jul 26, 2014 Online Instruction Global Online
A Tour of Health Canada Jul 26, 2014 Online Instruction Global Online
A Tour of Health Europe Jul 26, 2014 Online Instruction Global Online
Aspects of Regulatory History Jul 26, 2014 Online Instruction Global Online
Bioresearch Monitoring Program (BIMO): Introduction Jul 26, 2014 Online Instruction Global Online
The Clinical Development Process: Investigational Product, Plan, and Data Management Jul 26, 2014 Online Instruction Global Online
Drug Safety & Adverse Event Reporting Jul 26, 2014 Online Instruction Global Online
Ethical Review Boards Jul 26, 2014 Online Instruction Global Online
Ethics as the Foundation to Clinical Research Jul 26, 2014 Online Instruction Global Online
Awareness of FDA Inspections for Pharmaceutical Manufacturers Jul 26, 2014 Online Instruction Global Online
Biotechnology: An Overview of Compliance Considerations Jul 26, 2014 Online Instruction Global Online
Change Control Jul 26, 2014 Online Instruction Global Online
Clinical Trial Audits and Consequences of Non-Compliance Jul 26, 2014 Online Instruction Global Online
Computerized Systems Inspections in the Medical Device Industry Jul 26, 2014 Online Instruction Global Online
European Union Clinical Trials Directive Jul 26, 2014 Online Instruction Global Online
GMP Principals of SOPs Jul 26, 2014 Online Instruction Global Online
GMP Updates - Enforcement Changes at the New FDA Jul 26, 2014 Online Instruction Global Online
GMPs for API Bulk Manufacturers Jul 26, 2014 Online Instruction Global Online
Good Clinical Practices (GCPs) for New Product Investigations Jul 26, 2014 Online Instruction Global Online
Good Laboratory Practices (GLPs) Jul 26, 2014 Online Instruction Global Online
GxPs Jul 26, 2014 Online Instruction Global Online
HIPAA - The Impact on Clinical Research Jul 26, 2014 Online Instruction Global Online
Introduction to GMPs Jul 26, 2014 Online Instruction Global Online
Investigational Product Development Jul 26, 2014 Online Instruction Global Online
ISO 14155: Obligations of Sponsors and Monitors for Medical Device Trials Jul 26, 2014 Online Instruction Global Online
Key Concepts of Process Validation Jul 26, 2014 Online Instruction Global Online
Laboratory Specimens for Clinical Research Jul 26, 2014 Online Instruction Global Online
Medical Device Safety Reporting Jul 26, 2014 Online Instruction Global Online
Orientation to GMP Compliance Jul 26, 2014 Online Instruction Global Online
Overview of the Clinical Research Process Jul 26, 2014 Online Instruction Global Online
Part 11: Electronic Records and Signatures - Application Jul 26, 2014 Online Instruction Global Online
Part 11: Electronic Records; Electronic Signatures Jul 26, 2014 Online Instruction Global Online
Principles of Good Documentation Jul 26, 2014 Online Instruction Global Online
Protection of Human Subjects in Clinical Trials Jul 26, 2014 Online Instruction Global Online
Selecting and Managing Clinical Contract Research Organizations (CROs) Jul 26, 2014 Online Instruction Global Online
Understanding Post-Approval Changes Jul 26, 2014 Online Instruction Global Online
Computerized Systems Inspections in the Pharmaceutical Industry Jul 26, 2014 Online Instruction Global Online
Basics of the PhRMA Code Jul 26, 2014 Online Instruction Global Online
Basics of AdvaMed Code Jul 26, 2014 Online Instruction Global Online
Eucomed Guidelines on Interactions with Healthcare Professionals Jul 26, 2014 Online Instruction Global Online
Introduction to Medical Device Health Care Compliance Jul 26, 2014 Online Instruction Global Online
Foreign Corrupt Practices Act Jul 26, 2014 Online Instruction Global Online
Global Anti-bribery Jul 26, 2014 Online Instruction Global Online
Variations to Marketing Authorisation in Europe Jul 26, 2014 Online Instruction Global Online
Registration of Monoclonal Antibodies Jul 26, 2014 Online Instruction Global Online
How to Gain Approval to Market a Generic Medicinal Product in the USA Jul 26, 2014 Online Instruction Global Online
Pharmacokinetics and Pharmacodynamics in Drug Registration Jul 26, 2014 Online Instruction Global Online
Measurement in Clinical Trials: An Examination of the FDA Position on Review of Clinical Outcome Assessments (COAs) Jul 26, 2014 Online Instruction Global Online
The Electronic Trial Master File: So Much More than Just a Secure Document Repository Jul 26, 2014 Online Instruction Global Online
Planning and Implementing Large Cardiovascular Outcomes Studies: Opportunities & Challenges Jul 26, 2014 Online Instruction Global Online
Press the Easy Button – Ensure Consistency and Compliance for your Documents through Automation Jul 26, 2014 Online Instruction Global Online
When Outsourcing Stops Making Sense Jul 26, 2014 Online Instruction Global Online
Complimentary Quintiles/DIA Webinar - Giving Your Study The Right Start Toward Success Through Optimal Country and Site Selection Jul 26, 2014 Online Instruction Global Online
Complimentary - Risk-Based Monitoring: Regulatory Expectation and Operational Application Jul 26, 2014 Online Instruction Global Online
Fundamentals of Project Management for Nonproject Managers Jul 26, 2014 Online Instruction Global Online
Planning and Managing Your Project Jul 26, 2014 Online Instruction Global Online
Change Management, Issues Management, Escalation Management Jul 26, 2014 Online Instruction Global Online
Project Risk Management: Dealing with the Certainty of Uncertainty Jul 26, 2014 Online Instruction Global Online
Team Building and Development Jul 26, 2014 Online Instruction Global Online
Preparing a Clinical Trial Budget Jul 26, 2014 Online Instruction Global Online
Introduction to the European Union Institutions and Regulatory Authority Jul 26, 2014 Online Instruction Global Online
Introduction to US Institutions and Regulatory Authority (FDA) Jul 26, 2014 Online Instruction Global Online
Introduction to Japanese Institutions and Regulatory Authorities Jul 26, 2014 Online Instruction Global Online
Overview of the CTD and eCTD Jul 26, 2014 Online Instruction Global Online
Introduction to the International Conference on Harmonisation (ICH) Jul 26, 2014 Online Instruction Global Online
The Regulatory Development of a Drug Jul 26, 2014 Online Instruction Global Online
Basics of Clinical Trials Jul 26, 2014 Online Instruction Global Online
How to Register Medicinal Products through the Centralized Procedure Jul 26, 2014 Online Instruction Global Online
How to Register Medicinal Products through the Mutual Recognition Procedure Jul 26, 2014 Online Instruction Global Online
How to Maintain Marketing Approvals in Europe for Centrally Authorised Products Jul 26, 2014 Online Instruction Global Online
How to Register a New Drug in the USA Jul 26, 2014 Online Instruction Global Online
How to Register Medicinal Products through the Decentralized Procedure Jul 26, 2014 Online Instruction Global Online
Access to Unapproved Drugs through Compassionate Use Jul 26, 2014 Online Instruction Global Online
Regulatory Requirements for the Conduct of Clinical Trials in Europe Jul 26, 2014 Online Instruction Global Online
Orphan Drugs in the USA, European Union, and Japan Jul 26, 2014 Online Instruction Global Online
Regulatory Requirements for the Submission of Investigational New Drug Applications in the USA (INDs) Jul 26, 2014 Online Instruction Global Online
Meeting Opportunities with Regulatory Agencies Jul 26, 2014 Online Instruction Global Online
A Regulatory Perspective of Biosimilars in Emerging Markets Jul 26, 2014 Online Instruction Global Online
Combination Products and Convergence: An Overview of Clinical Benefits, Regulatory Issues & Manufacturing Challenges Jul 26, 2014 Online Instruction Global Online
Strategies for Successfully Introducing REMS to Your Organization: From Development and Implementation and Internal and External Evaluation Jul 26, 2014 Online Instruction Global Online
The Case of the New England Compounding Center: Learning from the Tragedy Jul 26, 2014 Online Instruction Global Online
Complimentary - From the Clinic to the CFO: Adaptive Trials and Financial Decision-Making Jul 26, 2014 Online Instruction Global Online
Complimentary - The Affiliate Challenge – How to Improve Compliance and Efficiency when Working with Regional Affiliates Jul 26, 2014 Online Instruction Global Online
The Future of Personalized Medicine and Companion Diagnostics Jul 26, 2014 Online Instruction Global Online
Seven-Part Series on Pediatric Drug Development - Part 1: Overall Challenge: The Vision of Better Medicines for Children Jul 26, 2014 Online Instruction Global Online
Seven-Part Series on Pediatric Drug Development - Part III: Regulatory Framework EU Jul 26, 2014 Online Instruction Global Online
Seven-Part Pediatric Drug Development Webinar Series - Part IV: Dosing in Children Jul 26, 2014 Online Instruction Global Online
Seven-Part Series on Pediatric Drug Development - Part II Regulatory Framework US Overview Jul 26, 2014 Online Instruction Global Online
Basics of the IND Jul 26, 2014 Online Instruction Global Online
Basics of the NDA Jul 26, 2014 Online Instruction Global Online
Regulatory Aspects of Prescription Drug/Biologics Advertising and Promotional Labeling Jul 26, 2014 Online Instruction Global Online
The Current State of Quality Oversight (QO) in the Pharmaceutical Industry Jul 26, 2014 Online Instruction Global Online
Supplements and Other Changes to an Approved Application Jul 26, 2014 Online Instruction Global Online
Planning and Managing Your Projects Jul 29, 2014 IACET, PMI Online Instruction Global Online
Five-Part Series on Fundamentals of Clinical Pharmacology for Drug Development - Part 2: Fundamentals of Clinical Pharmacology: Pharmacodynamics Aug 07, 2014 ACPE, IACET Online Instruction Global Online
Seven-Part Series on Pediatric Drug Development - Part V: Technical Development: Pediatric Formulations Aug 12, 2014 ACPE, IACET Online Instruction Global Online
Team Building and Development Aug 13, 2014 IACET, PMI Online Instruction Global Online
Pragmatic Approaches to Drug Safety Across the Premarketing and Postmarketing Continuum Aug 18, 2014 ACPE, IACET In-Person Instruction North America Boston, MA, United States
Regulatory Affairs: The IND, NDA, and Postmarketing Aug 18, 2014 IACET In-Person Instruction North America Boston, MA, United States
Clinical Project Management Aug 18, 2014 IACET, PMI In-Person Instruction North America Boston, MA, United States
New Drug Product Development and Life Cycle Management Aug 18, 2014 IACET, PMI In-Person Instruction North America Boston, MA, United States
European Regulatory Affairs: Keeping Your Finger on the Pulse of Marketing Authorizations Aug 18, 2014 IACET In-Person Instruction North America Boston, MA, United States
Project Risk Management Aug 20, 2014 IACET, PMI In-Person Instruction North America Boston, MA, United States
Five-Part Series on Fundamentals of Clinical Pharmacology For Drug Development - Part 3: Principles of Modeling and Simulation Sep 04, 2014 ACPE, IACET Online Instruction Global Online
Overview of Drug Development Sep 08, 2014 IACET, PMI In-Person Instruction North America Horsham, PA, United States
Key Considerations for the Development and Marketing of Biosimilar Products Sep 09, 2014 IACET In-Person Instruction North America Horsham, PA, United States
Clinical Trials Transparency 3-Part Series: Moving the Debate Forward - Realizing the Benefits of Providing Greater Access to Clinical Trial Data: Part 1 - Paving the Way for Greater Access To Data Sep 09, 2014 Online Instruction Global Online
Seven-Part Series on Pediatric Drug Development - Part VI: Preclinical Toxicology & Safety Sep 09, 2014 ACPE, IACET Online Instruction Global Online
Art of Writing a Clinical Overview Sep 09, 2014 IACET Online Instruction Global Online
Development of a Clinical Study Report Sep 15, 2014 IACET In-Person Instruction North America Rockville, MD, United States
Clinical Statistics for Nonstatisticians Sep 15, 2014 ACPE, IACET In-Person Instruction North America Rockville, MD, United States
Global Regulatory Strategy and Drug Development in Asia-Pacific, Latin America and Other Emerging Markets Sep 15, 2014 IACET In-Person Instruction North America Rockville, MD, United States
DIA Biosimilars 2014 Sep 18, 2014 ACPE, IACET Meetings North America Washington, DC, United States
EDM and ERS 2014 Sep 22, 2014 Meetings North America Washington, DC, United States
Strategies for Good Clinical Practice Audits Sep 23, 2014 IACET, RN Online Instruction Global Online
Introduction to Signal Detection and Data Mining Sep 29, 2014 IACET Online Instruction Global Online
Pharmacovigilance and Risk Management Planning Oct 01, 2014 ACPE, IACET In-Person Instruction North America
DIA Canadian Pharmacovigilance & Risk Management Oct 02, 2014 IACET Meetings North America
Five-Part Series on Fundamentals of Clinical Pharmacology for Drug Development - Part 4: Determining the Safe First Human Dose Oct 09, 2014 ACPE, IACET Online Instruction Global Online
Seven-Part Series on Pediatric Drug Development - Part VII: Operational Challenges of Pediatric Clinical Trials Oct 14, 2014 ACPE, IACET Online Instruction Global Online
Regulatory Affairs for Biologics Oct 19, 2014 IACET In-Person Instruction North America Irvine, CA, United States
Postmarketing Drug Safety and Pharmacovigilance Oct 20, 2014 ACPE, IACET In-Person Instruction North America Horsham, PA, United States
Adaptive Design in Clinical Trials: When and How to Apply Oct 21, 2014 In-Person Instruction North America Philadelphia, PA, United States
Clinical Trials Transparency 3-Part Series: Moving the Debate Forward - Realizing the Benefits of Providing Greater Access to Clinical Trial Data: Part 2 - Connecting the Research Community: Data Sharing – Perspectives from Academia and Patient Advocacy Oct 21, 2014 Online Instruction Global Online
Risk Management Plans and Drug Utilization Studies in Canada Oct 27, 2014 In-Person Instruction North America Ottawa, ON, Canada
DIA’s Annual Canadian Meeting: Thinking Globally, Acting Locally for The Well-Being of the Patient Oct 28, 2014 Meetings North America Ottawa, ON, Canada
Patient Engagement throughout the Full Spectrum of Drug Development: An Interactive Workshop for Life Science Companies and Patient Groups Oct 29, 2014 Meetings North America Washington, DC, United States
DIA Meeting on Combination Products Oct 29, 2014 IACET Meetings North America Washington, DC, United States
DIA Meeting on Companion Diagnostics Oct 30, 2014 IACET Meetings North America Washington, DC, United States
Negotiation and Influence Oct 30, 2014 IACET, PMI Online Instruction Global Online
Advanced Signal Detection - Tools, Triage, Evaluation, and Escalation Nov 03, 2014 In-Person Instruction North America Washington, DC, United States
Navigating Chemistry, Manufacturing & Controls Through the Drug Development Process Nov 03, 2014 IACET In-Person Instruction North America Horsham, PA, United States
Tutorial 1: From the Pediatric Case Files of FDA Nov 06, 2014 In-Person Instruction North America North Bethesda, MD, United States
Five-Part Series on Fundamentals of Clinical Pharmacology for Drug Development - Part 5: Assessment of QT Prolongation Nov 06, 2014 ACPE, IACET Online Instruction Global Online
Pediatric Research Conference 2014: Transforming the Pediatric Research Landscape through Innovation and Forward Thinking Nov 06, 2014 Meetings North America North Bethesda, MD, United States
Electronic Submissions: The Next Era of Electronic Submissions Nov 09, 2014 IACET In-Person Instruction North America Bethesda, MD, United States
Regulatory Affairs: The IND, NDA, and Postmarketing Nov 10, 2014 IACET In-Person Instruction North America Bethesda, MD, United States
The Leadership Experience Nov 10, 2014 IACET, PMI In-Person Instruction North America Bethesda, MD, United States
Risk Management and Safety Communication Strategies Nov 10, 2014 ACPE, IACET In-Person Instruction North America Bethesda, MD, United States
Clinical Trials Transparency 3-Part Series: Part 3 - Understanding the Legislation Landscape: Regulatory Updates from the FDA and EMA Nov 12, 2014 Online Instruction Global Online
Pharmacovigilance and Risk Management Strategies 2015 Jan 26, 2015 Meetings North America Washington, DC, United States
CMC Workshop 2015 Apr 13, 2015 Meetings North America Washington, DC, United States
DIA 2015 51st Annual Meeting Jun 14, 2015 Meetings North America Washington, DC, United States