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DIA
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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.

Find Meetings & Training 

Name Start Date Credits Format Region Location
EDM and ERS 2014 Sep 22, 2014 IACET Meetings North America Washington, DC, United States
Clinical Investigator: Module 2 - Conducting The Study Sep 23, 2014 ACPE, CME Online Instruction North America Online
Clinical Investigator: Module 1 - Study Preparation and Initiation Sep 23, 2014 ACPE, CME Online Instruction North America Online
Informed Consent Sep 23, 2014 ACPE Online Instruction North America Online
Crisis Management Sep 23, 2014 ACPE, IACET Online Instruction North America Online
Database Management Sep 23, 2014 ACPE, IACET Online Instruction North America Online
Literature Evaluation Sep 23, 2014 ACPE, IACET Online Instruction North America Online
Literature Searching Sep 23, 2014 ACPE, IACET Online Instruction North America Online
Medical Inquiries Sep 23, 2014 ACPE, IACET Online Instruction North America Online
Medical Writing Sep 23, 2014 IACET Online Instruction North America Online
Product Labeling Sep 23, 2014 ACPE, IACET Online Instruction North America Online
Regulatory Issues Sep 23, 2014 ACPE, IACET Online Instruction North America Online
Statistics for Medical Communications Professionals Sep 23, 2014 ACPE, IACET Online Instruction North America Online
The Use of Mobile Medical Applications as Companions Sep 23, 2014 Online Instruction Global Online
Generic Drug Labeling Proposed Rule and Safety Updates Sep 23, 2014 Online Instruction Global Online
Emerging Technologies to Rare Disorder Drug Development: Promises and Pitfalls Sep 23, 2014 Online Instruction Global Online
Big Data: Impact of Health Care Reform on Collaborations and Strategies Sep 23, 2014 Online Instruction Global Online
Implementation of the FDASIA Patient Provisions Sep 23, 2014 Online Instruction Global Online
Complimentary: Regulatory and Real World Evidence Challenges of Rare Diseases and Orphan Drugs Sep 23, 2014 Online Instruction Global Online
Variations in the European Union: CMC/Quality Changes Sep 23, 2014 Online Instruction Global Online
Good Pharmacovigilance Practice: How Good has it Proven to be for Industry? Sep 23, 2014 Online Instruction Global Online
Pharmacovigilance and Risk Management: Patient Perspective Sep 23, 2014 Online Instruction Global Online
Complimentary Patient-Centeredness and Engagement in Clinical Research: Opportunities for Industry Sep 23, 2014 Online Instruction Global Online
Drug Safety Regulatory Requirements Sep 23, 2014 ACPE, IACET Online Instruction Global Online
Premarketing Clinical Trial Safety Sep 23, 2014 ACPE, IACET Online Instruction Global Online
Postmarketing Safety Management Sep 23, 2014 Online Instruction Global Online
Basics of Signal Detection and Pharmacoepidemiology Sep 23, 2014 ACPE, IACET Online Instruction Global Online
Safety Audits and Inspections Sep 23, 2014 Online Instruction Global Online
Five-Part Series on Fundamentals of Clinical Pharmacology for Drug Development - Part 1: Fundamentals of Clinical Pharmacology: Pharmacokinetics Sep 23, 2014 Online Instruction Global Online
Five-Part Series on Fundamentals of Clinical Pharmacology for Drug Development - Part 2: Fundamentals of Clinical Pharmacology: Pharmacodynamics Sep 23, 2014 Online Instruction Global Online
Pharmacovigilance and Global Harmonization Updates Sep 23, 2014 Online Instruction Global Online
Five-Part Series on Fundamentals of Clinical Pharmacology For Drug Development - Part 3: Principles of Modeling and Simulation Sep 23, 2014 Online Instruction Global Online
Designed for Success: Utilizing Protocol Quality by Design (QbD) to Plan Clinical Studies Sep 23, 2014 Online Instruction Global Online
Negotiation and Influence Sep 23, 2014 Online Instruction Global Online
China Update: Regulatory Changes and Implications Sep 23, 2014 Online Instruction Global Online
Evaluation and Management of Cardiac Conditions in Oncology Patients Sep 23, 2014 Online Instruction Global Online
Risk Management of Medicinal Products: REMS and RMP - Need for Harmonization Within the ICH Region? Sep 23, 2014 Online Instruction Global Online
Introduction to Drug Safety Sep 23, 2014 ACPE, IACET Online Instruction Global Online
How to Prepare for a Safety Inspection Sep 23, 2014 Online Instruction Global Online
Clinical Statistics for Nonstatisticians Sep 23, 2014 Online Instruction Global Online
Advanced Clinical Statistics for Nonstatisticians Sep 23, 2014 Online Instruction Global Online
Development of a Clinical Study Report Sep 23, 2014 Online Instruction Global Online
Art of Writing a Clinical Overview Sep 23, 2014 Online Instruction Global Online
CardioVascular Safety: The New Paradigm - Proarrhythmic Assessment of New Drugs without the Thorough QT Study Sep 23, 2014 Online Instruction Global Online
CardioVascular Safety – What are the Key Issues Regarding Blood Pressure Assessment During Clinical Development Sep 23, 2014 Online Instruction Global Online
Introductory Principles and Application of Risk Management within Clinical Operations Sep 23, 2014 Online Instruction Global Online
Seven-Part Series on Pediatric Drug Development - Part VI: Preclinical Toxicology & Safety Sep 23, 2014 Online Instruction Global Online
Electronic Submissions 101 – Essential MS Word and Adobe Acrobat Tools/Skills and Current IT Options Sep 23, 2014 Online Instruction Global Online
A Tour of FDA Sep 23, 2014 Online Instruction Global Online
A Tour of Health Canada Sep 23, 2014 Online Instruction Global Online
A Tour of Health Europe Sep 23, 2014 Online Instruction Global Online
Aspects of Regulatory History Sep 23, 2014 Online Instruction Global Online
Bioresearch Monitoring Program (BIMO): Introduction Sep 23, 2014 Online Instruction Global Online
The Clinical Development Process: Investigational Product, Plan, and Data Management Sep 23, 2014 Online Instruction Global Online
Drug Safety & Adverse Event Reporting Sep 23, 2014 Online Instruction Global Online
Ethical Review Boards Sep 23, 2014 Online Instruction Global Online
Ethics as the Foundation to Clinical Research Sep 23, 2014 Online Instruction Global Online
Awareness of FDA Inspections for Pharmaceutical Manufacturers Sep 23, 2014 Online Instruction Global Online
Biotechnology: An Overview of Compliance Considerations Sep 23, 2014 Online Instruction Global Online
Change Control Sep 23, 2014 Online Instruction Global Online
Clinical Trial Audits and Consequences of Non-Compliance Sep 23, 2014 Online Instruction Global Online
Computerized Systems Inspections in the Medical Device Industry Sep 23, 2014 Online Instruction Global Online
European Union Clinical Trials Directive Sep 23, 2014 Online Instruction Global Online
GMP Principals of SOPs Sep 23, 2014 Online Instruction Global Online
GMP Updates - Enforcement Changes at the New FDA Sep 23, 2014 Online Instruction Global Online
GMPs for API Bulk Manufacturers Sep 23, 2014 Online Instruction Global Online
Good Clinical Practices (GCPs) for New Product Investigations Sep 23, 2014 Online Instruction Global Online
Good Laboratory Practices (GLPs) Sep 23, 2014 Online Instruction Global Online
GxPs Sep 23, 2014 Online Instruction Global Online
HIPAA - The Impact on Clinical Research Sep 23, 2014 Online Instruction Global Online
Introduction to GMPs Sep 23, 2014 Online Instruction Global Online
Investigational Product Development Sep 23, 2014 Online Instruction Global Online
ISO 14155: Obligations of Sponsors and Monitors for Medical Device Trials Sep 23, 2014 Online Instruction Global Online
Key Concepts of Process Validation Sep 23, 2014 Online Instruction Global Online
Laboratory Specimens for Clinical Research Sep 23, 2014 Online Instruction Global Online
Medical Device Safety Reporting Sep 23, 2014 Online Instruction Global Online
Orientation to GMP Compliance Sep 23, 2014 Online Instruction Global Online
Overview of the Clinical Research Process Sep 23, 2014 Online Instruction Global Online
Part 11: Electronic Records and Signatures - Application Sep 23, 2014 Online Instruction Global Online
Part 11: Electronic Records; Electronic Signatures Sep 23, 2014 Online Instruction Global Online
Principles of Good Documentation Sep 23, 2014 Online Instruction Global Online
Protection of Human Subjects in Clinical Trials Sep 23, 2014 Online Instruction Global Online
Selecting and Managing Clinical Contract Research Organizations (CROs) Sep 23, 2014 Online Instruction Global Online
Understanding Post-Approval Changes Sep 23, 2014 Online Instruction Global Online
Computerized Systems Inspections in the Pharmaceutical Industry Sep 23, 2014 Online Instruction Global Online
Basics of the PhRMA Code Sep 23, 2014 Online Instruction Global Online
Basics of AdvaMed Code Sep 23, 2014 Online Instruction Global Online
Eucomed Guidelines on Interactions with Healthcare Professionals Sep 23, 2014 Online Instruction Global Online
Introduction to Medical Device Health Care Compliance Sep 23, 2014 Online Instruction Global Online
Foreign Corrupt Practices Act Sep 23, 2014 Online Instruction Global Online
Global Anti-bribery Sep 23, 2014 Online Instruction Global Online
Variations to Marketing Authorisation in Europe Sep 23, 2014 Online Instruction Global Online
Registration of Monoclonal Antibodies Sep 23, 2014 Online Instruction Global Online
How to Gain Approval to Market a Generic Medicinal Product in the USA Sep 23, 2014 Online Instruction Global Online
Pharmacokinetics and Pharmacodynamics in Drug Registration Sep 23, 2014 Online Instruction Global Online
Complimentary - Planning and Implementing Large Cardiovascular Outcomes Studies: Opportunities & Challenges Sep 23, 2014 Online Instruction Global Online
Complimentary - Press the Easy Button – Ensure Consistency and Compliance for your Documents through Automation Sep 23, 2014 Online Instruction Global Online
Complimentary - When Outsourcing Stops Making Sense Sep 23, 2014 Online Instruction Global Online
Complimentary Quintiles/DIA Webinar - Giving Your Study The Right Start Toward Success Through Optimal Country and Site Selection Sep 23, 2014 Online Instruction Global Online
Complimentary - Risk-Based Monitoring: Regulatory Expectation and Operational Application Sep 23, 2014 Online Instruction Global Online
Fundamentals of Project Management for Nonproject Managers Sep 23, 2014 Online Instruction Global Online
Planning and Managing Your Project Sep 23, 2014 Online Instruction Global Online
Planning and Managing Your Projects Sep 23, 2014 Online Instruction Global Online
Change Management, Issues Management, Escalation Management Sep 23, 2014 Online Instruction Global Online
Project Risk Management: Dealing with the Certainty of Uncertainty Sep 23, 2014 Online Instruction Global Online
Team Building and Development Sep 23, 2014 Online Instruction Global Online
Preparing a Clinical Trial Budget Sep 23, 2014 Online Instruction Global Online
Team Building and Development Sep 23, 2014 Online Instruction Global Online
Introduction to the European Union Institutions and Regulatory Authority Sep 23, 2014 Online Instruction Global Online
Introduction to US Institutions and Regulatory Authority (FDA) Sep 23, 2014 Online Instruction Global Online
Introduction to Japanese Institutions and Regulatory Authorities Sep 23, 2014 Online Instruction Global Online
Overview of the CTD and eCTD Sep 23, 2014 Online Instruction Global Online
Introduction to the International Conference on Harmonisation (ICH) Sep 23, 2014 Online Instruction Global Online
The Regulatory Development of a Drug Sep 23, 2014 Online Instruction Global Online
Basics of Clinical Trials Sep 23, 2014 Online Instruction Global Online
How to Register Medicinal Products through the Centralized Procedure Sep 23, 2014 Online Instruction Global Online
How to Register Medicinal Products through the Mutual Recognition Procedure Sep 23, 2014 Online Instruction Global Online
How to Maintain Marketing Approvals in Europe for Centrally Authorised Products Sep 23, 2014 Online Instruction Global Online
How to Register a New Drug in the USA Sep 23, 2014 Online Instruction Global Online
How to Register Medicinal Products through the Decentralized Procedure Sep 23, 2014 Online Instruction Global Online
Access to Unapproved Drugs through Compassionate Use Sep 23, 2014 Online Instruction Global Online
Regulatory Requirements for the Conduct of Clinical Trials in Europe Sep 23, 2014 Online Instruction Global Online
Orphan Drugs in the USA, European Union, and Japan Sep 23, 2014 Online Instruction Global Online
Regulatory Requirements for the Submission of Investigational New Drug Applications in the USA (INDs) Sep 23, 2014 Online Instruction Global Online
Meeting Opportunities with Regulatory Agencies Sep 23, 2014 Online Instruction Global Online
Combination Products and Convergence: An Overview of Clinical Benefits, Regulatory Issues & Manufacturing Challenges Sep 23, 2014 Online Instruction Global Online
Strategies for Successfully Introducing REMS to Your Organization: From Development and Implementation and Internal and External Evaluation Sep 23, 2014 Online Instruction Global Online
The Case of the New England Compounding Center: Learning from the Tragedy Sep 23, 2014 Online Instruction Global Online
Complimentary - From the Clinic to the CFO: Adaptive Trials and Financial Decision-Making Sep 23, 2014 Online Instruction Global Online
Adverse Event Reporting Requirements: IND and Postmarketing Sep 23, 2014 Online Instruction Global Online
Complimentary - The Affiliate Challenge – How to Improve Compliance and Efficiency when Working with Regional Affiliates Sep 23, 2014 Online Instruction Global Online
The Future of Personalized Medicine and Companion Diagnostics Sep 23, 2014 Online Instruction Global Online
Seven-Part Series on Pediatric Drug Development - Part 1: Overall Challenge: The Vision of Better Medicines for Children Sep 23, 2014 Online Instruction Global Online
Seven-Part Series on Pediatric Drug Development - Part 3: Regulatory Framework EU Sep 23, 2014 Online Instruction Global Online
Seven-Part Pediatric Drug Development Webinar Series - Part 4: Dosing in Children Sep 23, 2014 Online Instruction Global Online
Seven-Part Series on Pediatric Drug Development - Part 2 Regulatory Framework US Overview Sep 23, 2014 Online Instruction Global Online
Seven-Part Series on Pediatric Drug Development - Part 5: Technical Development: Pediatric Formulations Sep 23, 2014 Online Instruction Global Online
Basics of the IND Sep 23, 2014 Online Instruction Global Online
Basics of the NDA Sep 23, 2014 Online Instruction Global Online
Regulatory Aspects of Prescription Drug/Biologics Advertising and Promotional Labeling Sep 23, 2014 Online Instruction Global Online
Seven-Part Series on Pediatric Drug Development - Part VII: Operational Challenges of Pediatric Clinical Trials Sep 23, 2014 Online Instruction Global Online
The Current State of Quality Oversight (QO) in the Pharmaceutical Industry Sep 23, 2014 Online Instruction Global Online
Supplements and Other Changes to an Approved Application Sep 23, 2014 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 Toronto, ON, Canada
DIA Canadian Pharmacovigilance & Risk Management Oct 02, 2014 IACET Meetings North America Toronto, ON, Canada
Disruptive Innovation in Medical Information Oct 06, 2014 ACPE, IACET Online Instruction Global Online
The Role of the Clinical Data Manager Oct 08, 2014 IACET Online Instruction Global Online
Facets of Drug-Induced Kidney Injury and Regulatory Perspective Oct 08, 2014 ACPE, IACET Online Instruction Global Online
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
Fact or Fiction: Legal Restrictions to Patient Engagement in Drug Development Oct 14, 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 IACET 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 Groups Oct 21, 2014 IACET Online Instruction Global Online
Complimentary - Moving Your Regulated Content Management Platform to the Cloud: Benefits & Barriers Oct 22, 2014 Online Instruction Global Online
Biostatistics for Non-Statisticians Oct 27, 2014 IACET In-Person Instruction North America
Risk Management Plans and Drug Utilization Studies in Canada Oct 27, 2014 IACET 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
Combination Products: A Comprehensive Overview of Premarket Opportunities and Postmarket Challenges! Oct 28, 2014 IACET In-Person Instruction North America Washington, DC, United States
Patient Engagement throughout the Full Spectrum of Drug Development: An Interactive Workshop for Life Science Companies and Patient Groups Oct 29, 2014 IACET 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
Navigating Chemistry, Manufacturing & Controls Through the Drug Development Process Nov 03, 2014 IACET In-Person Instruction North America Horsham, PA, United States
Advanced Signal Detection - Tools, Triage, Evaluation, and Escalation Nov 03, 2014 IACET In-Person Instruction North America Washington, DC, United States
From the Pediatric Case Files of FDA Nov 06, 2014 IACET 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 IACET 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
Optimizing Financial Management to Maximize Clinical Trial Investments Nov 11, 2014 Meetings 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 3 - Understanding the Legislation Landscape: Regulatory Updates from the FDA and EMA Nov 12, 2014 IACET Online Instruction Global Online
Proarrhythmia Nov 19, 2014 ACPE, IACET Online Instruction Global Online
Impact on Drug Development of Novel Translational Safety Biomarkers for Improved Detection of Drug-Induced Acute Kidney Injury Nov 20, 2014 ACPE, IACET Online Instruction Global Online
The Basics of Clinical Data Management From Start to End Dec 03, 2014 IACET In-Person Instruction North America Washington, DC, United States
Pharmacovigilance and Risk Management Strategies 2015 Jan 26, 2015 Meetings North America Washington, DC, United States
Joint Adaptive Design and Bayesian Statistics Conference: Drivers of Efficiency in Modern Medical Product Development Feb 10, 2015 Meetings North America Arlington, VA, United States
Marketing Pharmaceuticals 2015 Feb 17, 2015 Meetings North America Washington, DC, United States
CMC Workshop 2015 Apr 13, 2015 Meetings North America Bethesda, MD, United States
DIA/FDA Statistics Forum 2015 Apr 20, 2015 Meetings North America North Bethesda, MD, United States
DIA 2015 51st Annual Meeting: Develop. Innovate. Advance. Jun 14, 2015 Meetings North America Washington, DC, United States