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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
Advanced Clinical Statistics for Nonstatisticians Jul 15, 2014 ACPE, IACET Online Instruction Global Online
Adverse Event Reporting Requirements: IND and Postmarketing Jul 22, 2014 IACET Online Instruction Global Online
The Use of Mobile Medical Applications as Companions Jul 23, 2014 Online Instruction Global Online
Regulating a Social World Jul 23, 2014 Online Instruction Global Online
Generic Drug Labeling Proposed Rule and Safety Updates Jul 23, 2014 Online Instruction Global Online
English Literacy and Spanish Transcreation of Patient Documents: Concepts for Low Literacy Materials Jul 23, 2014 Online Instruction Global Online
Big Data: Impact of Health Care Reform on Collaborations and Strategies Jul 23, 2014 Online Instruction Global Online
Implementation of the FDASIA Patient Provisions Jul 23, 2014 Online Instruction Global Online
Complimentary: Regulatory and Real World Evidence Challenges of Rare Diseases and Orphan Drugs Jul 23, 2014 Online Instruction Global Online
Variations in the European Union: CMC/Quality Changes Jul 23, 2014 Online Instruction Global Online
Good Pharmacovigilance Practice: How Good has it Proven to be for Industry? Jul 23, 2014 Online Instruction Global Online
Safety and Social Media: Is this the Question or the Answer Jul 23, 2014 Online Instruction Global Online
Pharmacovigilance and Risk Management: Patient Perspective Jul 23, 2014 Online Instruction Global Online
Complimentary Patient-Centeredness and Engagement in Clinical Research: Opportunities for Industry Jul 23, 2014 Online Instruction Global Online
Drug Safety Regulatory Requirements Jul 23, 2014 ACPE, IACET Online Instruction Global Online
Premarketing Clinical Trial Safety Jul 23, 2014 ACPE, IACET Online Instruction Global Online
Postmarketing Safety Management Jul 23, 2014 Online Instruction Global Online
Basics of Signal Detection and Pharmacoepidemiology Jul 23, 2014 Online Instruction Global Online
Safety Audits and Inspections Jul 23, 2014 Online Instruction Global Online
Five-Part Series on Fundamentals of Clinical Pharmacology for Drug Development - Part 1: Fundamentals of Clinical Pharmacology: Pharmacokinetics Jul 23, 2014 Online Instruction Global Online
Designed for Success: Utilizing Protocol Quality by Design (QbD) to Plan Clinical Studies Jul 23, 2014 Online Instruction Global Online
Negotiation and Influence Jul 23, 2014 Online Instruction Global Online
China Update: Regulatory Changes and Implications Jul 23, 2014 Online Instruction Global Online
Evaluation and Management of Cardiac Conditions in Oncology Patients Jul 23, 2014 Online Instruction Global Online
Risk Management of Medicinal Products: REMS and RMP - Need for Harmonization Within the ICH Region? Jul 23, 2014 Online Instruction Global Online
Introduction to Drug Safety Jul 23, 2014 ACPE, IACET Online Instruction Global Online
How to Prepare for a Safety Inspection Jul 23, 2014 Online Instruction Global Online
CDER Town Meeting: Safety Hot Topics Jul 23, 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 23, 2014 Online Instruction Global Online
Assessing the Benefits and Risks of Medicines: Webinar Series Part 2 - Benefit-Risk Assessment a Changing Regulatory Landscape Jul 23, 2014 Online Instruction Global Online
Assessing the Benefits and Risks of Medicines: Webinar Series - Part 3: Framing for Benefit-Risk Assessment and Communication Jul 23, 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 23, 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 23, 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 23, 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 23, 2014 Online Instruction Global Online
Assessing the Benefits and Risks of Medicines: Webinar Series- Part 8: Visualization and Communication of Benefit-Risk Jul 23, 2014 Online Instruction Global Online
New Good Pharmacovigilance Practice (GVP) Documents in Canada Jul 23, 2014 Online Instruction Global Online
Clinical Statistics for Nonstatisticians Jul 23, 2014 Online Instruction Global Online
Development of a Clinical Study Report Jul 23, 2014 Online Instruction Global Online
Complimentary Biomarker Strategies for More Efficient Early-Phase Drug Development in Alzheimer's Disease Jul 23, 2014 Online Instruction Global Online
CardioVascular Safety: The New Paradigm - Proarrhythmic Assessment of New Drugs without the Thorough QT Study Jul 23, 2014 Online Instruction Global Online
CardioVascular Safety – What are the Key Issues Regarding Blood Pressure Assessment During Clinical Development Jul 23, 2014 Online Instruction Global Online
Introductory Principles and Application of Risk Management within Clinical Operations Jul 23, 2014 Online Instruction Global Online
Electronic Submissions 101 – Essential MS Word and Adobe Acrobat Tools/Skills and Current IT Options Jul 23, 2014 Online Instruction Global Online
A Tour of FDA Jul 23, 2014 Online Instruction Global Online
A Tour of Health Canada Jul 23, 2014 Online Instruction Global Online
A Tour of Health Europe Jul 23, 2014 Online Instruction Global Online
Aspects of Regulatory History Jul 23, 2014 Online Instruction Global Online
Bioresearch Monitoring Program (BIMO): Introduction Jul 23, 2014 Online Instruction Global Online
The Clinical Development Process: Investigational Product, Plan, and Data Management Jul 23, 2014 Online Instruction Global Online
Drug Safety & Adverse Event Reporting Jul 23, 2014 Online Instruction Global Online
Ethical Review Boards Jul 23, 2014 Online Instruction Global Online
Ethics as the Foundation to Clinical Research Jul 23, 2014 Online Instruction Global Online
Awareness of FDA Inspections for Pharmaceutical Manufacturers Jul 23, 2014 Online Instruction Global Online
Biotechnology: An Overview of Compliance Considerations Jul 23, 2014 Online Instruction Global Online
Change Control Jul 23, 2014 Online Instruction Global Online
Clinical Trial Audits and Consequences of Non-Compliance Jul 23, 2014 Online Instruction Global Online
Computerized Systems Inspections in the Medical Device Industry Jul 23, 2014 Online Instruction Global Online
European Union Clinical Trials Directive Jul 23, 2014 Online Instruction Global Online
GMP Principals of SOPs Jul 23, 2014 Online Instruction Global Online
GMP Updates - Enforcement Changes at the New FDA Jul 23, 2014 Online Instruction Global Online
GMPs for API Bulk Manufacturers Jul 23, 2014 Online Instruction Global Online
Good Clinical Practices (GCPs) for New Product Investigations Jul 23, 2014 Online Instruction Global Online
Good Laboratory Practices (GLPs) Jul 23, 2014 Online Instruction Global Online
GxPs Jul 23, 2014 Online Instruction Global Online
HIPAA - The Impact on Clinical Research Jul 23, 2014 Online Instruction Global Online
Introduction to GMPs Jul 23, 2014 Online Instruction Global Online
Investigational Product Development Jul 23, 2014 Online Instruction Global Online
ISO 14155: Obligations of Sponsors and Monitors for Medical Device Trials Jul 23, 2014 Online Instruction Global Online
Key Concepts of Process Validation Jul 23, 2014 Online Instruction Global Online
Laboratory Specimens for Clinical Research Jul 23, 2014 Online Instruction Global Online
Medical Device Safety Reporting Jul 23, 2014 Online Instruction Global Online
Orientation to GMP Compliance Jul 23, 2014 Online Instruction Global Online
Overview of the Clinical Research Process Jul 23, 2014 Online Instruction Global Online
Part 11: Electronic Records and Signatures - Application Jul 23, 2014 Online Instruction Global Online
Part 11: Electronic Records; Electronic Signatures Jul 23, 2014 Online Instruction Global Online
Principles of Good Documentation Jul 23, 2014 Online Instruction Global Online
Protection of Human Subjects in Clinical Trials Jul 23, 2014 Online Instruction Global Online
Selecting and Managing Clinical Contract Research Organizations (CROs) Jul 23, 2014 Online Instruction Global Online
Understanding Post-Approval Changes Jul 23, 2014 Online Instruction Global Online
Computerized Systems Inspections in the Pharmaceutical Industry Jul 23, 2014 Online Instruction Global Online
Basics of the PhRMA Code Jul 23, 2014 Online Instruction Global Online
Basics of AdvaMed Code Jul 23, 2014 Online Instruction Global Online
Eucomed Guidelines on Interactions with Healthcare Professionals Jul 23, 2014 Online Instruction Global Online
Introduction to Medical Device Health Care Compliance Jul 23, 2014 Online Instruction Global Online
Foreign Corrupt Practices Act Jul 23, 2014 Online Instruction Global Online
Global Anti-bribery Jul 23, 2014 Online Instruction Global Online
Variations to Marketing Authorisation in Europe Jul 23, 2014 Online Instruction Global Online
Registration of Monoclonal Antibodies Jul 23, 2014 Online Instruction Global Online
How to Gain Approval to Market a Generic Medicinal Product in the USA Jul 23, 2014 Online Instruction Global Online
Pharmacokinetics and Pharmacodynamics in Drug Registration Jul 23, 2014 Online Instruction Global Online
Measurement in Clinical Trials: An Examination of the FDA Position on Review of Clinical Outcome Assessments (COAs) Jul 23, 2014 Online Instruction Global Online
The Electronic Trial Master File: So Much More than Just a Secure Document Repository Jul 23, 2014 Online Instruction Global Online
Planning and Implementing Large Cardiovascular Outcomes Studies: Opportunities & Challenges Jul 23, 2014 Online Instruction Global Online
Press the Easy Button – Ensure Consistency and Compliance for your Documents through Automation Jul 23, 2014 Online Instruction Global Online
When Outsourcing Stops Making Sense Jul 23, 2014 Online Instruction Global Online
Complimentary Quintiles/DIA Webinar - Giving Your Study The Right Start Toward Success Through Optimal Country and Site Selection Jul 23, 2014 Online Instruction Global Online
Complimentary - Risk-Based Monitoring: Regulatory Expectation and Operational Application Jul 23, 2014 Online Instruction Global Online
Fundamentals of Project Management for Nonproject Managers Jul 23, 2014 Online Instruction Global Online
Planning and Managing Your Project Jul 23, 2014 Online Instruction Global Online
Change Management, Issues Management, Escalation Management Jul 23, 2014 Online Instruction Global Online
Project Risk Management: Dealing with the Certainty of Uncertainty Jul 23, 2014 Online Instruction Global Online
Team Building and Development Jul 23, 2014 Online Instruction Global Online
Preparing a Clinical Trial Budget Jul 23, 2014 Online Instruction Global Online
Introduction to the European Union Institutions and Regulatory Authority Jul 23, 2014 Online Instruction Global Online
Introduction to US Institutions and Regulatory Authority (FDA) Jul 23, 2014 Online Instruction Global Online
Introduction to Japanese Institutions and Regulatory Authorities Jul 23, 2014 Online Instruction Global Online
Overview of the CTD and eCTD Jul 23, 2014 Online Instruction Global Online
Introduction to the International Conference on Harmonisation (ICH) Jul 23, 2014 Online Instruction Global Online
The Regulatory Development of a Drug Jul 23, 2014 Online Instruction Global Online
Basics of Clinical Trials Jul 23, 2014 Online Instruction Global Online
How to Register Medicinal Products through the Centralized Procedure Jul 23, 2014 Online Instruction Global Online
How to Register Medicinal Products through the Mutual Recognition Procedure Jul 23, 2014 Online Instruction Global Online
How to Maintain Marketing Approvals in Europe for Centrally Authorised Products Jul 23, 2014 Online Instruction Global Online
How to Register a New Drug in the USA Jul 23, 2014 Online Instruction Global Online
How to Register Medicinal Products through the Decentralized Procedure Jul 23, 2014 Online Instruction Global Online
Access to Unapproved Drugs through Compassionate Use Jul 23, 2014 Online Instruction Global Online
Regulatory Requirements for the Conduct of Clinical Trials in Europe Jul 23, 2014 Online Instruction Global Online
Orphan Drugs in the USA, European Union, and Japan Jul 23, 2014 Online Instruction Global Online
Regulatory Requirements for the Submission of Investigational New Drug Applications in the USA (INDs) Jul 23, 2014 Online Instruction Global Online
Meeting Opportunities with Regulatory Agencies Jul 23, 2014 Online Instruction Global Online
A Regulatory Perspective of Biosimilars in Emerging Markets Jul 23, 2014 Online Instruction Global Online
Combination Products and Convergence: An Overview of Clinical Benefits, Regulatory Issues & Manufacturing Challenges Jul 23, 2014 Online Instruction Global Online
Strategies for Successfully Introducing REMS to Your Organization: From Development and Implementation and Internal and External Evaluation Jul 23, 2014 Online Instruction Global Online
The Case of the New England Compounding Center: Learning from the Tragedy Jul 23, 2014 Online Instruction Global Online
Complimentary - From the Clinic to the CFO: Adaptive Trials and Financial Decision-Making Jul 23, 2014 Online Instruction Global Online
Complimentary - The Affiliate Challenge – How to Improve Compliance and Efficiency when Working with Regional Affiliates Jul 23, 2014 Online Instruction Global Online
The Future of Personalized Medicine and Companion Diagnostics Jul 23, 2014 Online Instruction Global Online
Seven-Part Series on Pediatric Drug Development - Part 1: Overall Challenge: The Vision of Better Medicines for Children Jul 23, 2014 Online Instruction Global Online
Seven-Part Series on Pediatric Drug Development - Part III: Regulatory Framework EU Jul 23, 2014 Online Instruction Global Online
Seven-Part Pediatric Drug Development Webinar Series - Part IV: Dosing in Children Jul 23, 2014 Online Instruction Global Online
Seven-Part Series on Pediatric Drug Development - Part II Regulatory Framework US Overview Jul 23, 2014 Online Instruction Global Online
Basics of the IND Jul 23, 2014 Online Instruction Global Online
Basics of the NDA Jul 23, 2014 Online Instruction Global Online
Regulatory Aspects of Prescription Drug/Biologics Advertising and Promotional Labeling Jul 23, 2014 Online Instruction Global Online
The Current State of Quality Oversight (QO) in the Pharmaceutical Industry Jul 23, 2014 Online Instruction Global Online
Supplements and Other Changes to an Approved Application Jul 23, 2014 Online Instruction Global Online
Pharmacovigilance and Global Harmonization Updates Jul 24, 2014 IACET 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
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
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
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
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
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
Negotiation and Influence Oct 30, 2014 IACET, PMI Online Instruction Global Online
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
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