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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.

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Name Start Date Credits Format Region Location
Clinical Investigator: Module 2 - Conducting the Study Jul 1, 2015 ACPE, CME Online Instruction North America Online
Clinical Investigator: Module 1 - Study Preparation and Initiation Jul 1, 2015 ACPE, CME Online Instruction North America Online
Informed Consent Jul 1, 2015 ACPE Online Instruction North America Online
Crisis Management Jul 1, 2015 ACPE, IACET Online Instruction North America Online
Database Management Jul 1, 2015 ACPE, IACET Online Instruction North America Online
Literature Evaluation Jul 1, 2015 ACPE, IACET Online Instruction North America Online
Literature Searching Jul 1, 2015 ACPE, IACET Online Instruction North America Online
Medical Inquiries Jul 1, 2015 ACPE, IACET Online Instruction North America Online
Medical Writing Jul 1, 2015 IACET Online Instruction North America Online
Product Labeling Jul 1, 2015 ACPE, IACET Online Instruction North America Online
Regulatory Issues Jul 1, 2015 ACPE, IACET Online Instruction North America Online
Statistics for Medical Communications Professionals Jul 1, 2015 ACPE, IACET Online Instruction North America Online
Expert Reactor Panel: IOM Report on Sharing Clinical Trial Data Jul 1, 2015 Online Instruction Global Online
Novel Data Sources: The Positive Impact of Social Media and Online Networks for Engaging with Patients Jul 1, 2015 Online Instruction Global Online
FDA’s Evolving Position on the Brief Summary and Adequate Directions for Use Guidance Jul 1, 2015 Online Instruction Global Online
Target Product Profile – Strategies to Optimize Drug Development, Product Labeling, and Commercialization Jul 1, 2015 Online Instruction Global Online
GVP Module IX Compliant Signal Management Systems in Pharmacovigilance: A Tale of Two Experiences Jul 1, 2015 Online Instruction Global Online
Complimentary Webinar - Using Revolutionary Machine Learning to Find the Most Relevant Content to Drive Informed Decisions in Regulatory Intelligence Jul 1, 2015 Online Instruction Global Online
The Role of the Clinical Data Manager Jul 1, 2015 Online Instruction Global Online
Complimentary: Regulatory and Real World Evidence Challenges of Rare Diseases and Orphan Drugs Jul 1, 2015 Online Instruction Global Online
FDA’s Role in Advancing the Science of Pharmacovigilance: Tools, Methods, and Pilot Programs Under Evaluation for the Analysis of Safety Signals Jul 1, 2015 Online Instruction Global Online
Proarrhythmia Jul 1, 2015 Online Instruction Global Online
Facets of Drug-Induced Kidney Injury and Regulatory Perspective Jul 1, 2015 Online Instruction Global Online
Impact on Drug Development of Novel Translational Safety Biomarkers for Improved Detection of Drug-Induced Acute Kidney Injury Jul 1, 2015 Online Instruction Global Online
A New Era of Open Dialog and Communication: The Impact of FDASIA, PDUFA V, and Critical Path Innovation Meetings Jul 1, 2015 Online Instruction Global Online
Pharmacovigilance and Risk Management: Patient Perspective Jul 1, 2015 Online Instruction Global Online
Drug Safety Regulatory Requirements Jul 1, 2015 ACPE, IACET Online Instruction Global Online
Premarketing Clinical Trial Safety Jul 1, 2015 ACPE, IACET Online Instruction Global Online
Postmarketing Safety Management Jul 1, 2015 ACPE, IACET Online Instruction Global Online
Basics of Signal Detection and Pharmacoepidemiology Jul 1, 2015 ACPE, IACET Online Instruction Global Online
Safety Audits and Inspections Jul 1, 2015 ACPE, IACET Online Instruction Global Online
Five-Part Series on Fundamentals of Clinical Pharmacology for Drug Development - Part 1: Fundamentals of Clinical Pharmacology: Pharmacokinetics Jul 1, 2015 Online Instruction Global Online
Five-Part Series on Fundamentals of Clinical Pharmacology for Drug Development - Part 2: Fundamentals of Clinical Pharmacology: Pharmacodynamics Jul 1, 2015 Online Instruction Global Online
Pharmacovigilance and Global Harmonization Updates Jul 1, 2015 Online Instruction Global Online
Five-Part Series on Fundamentals of Clinical Pharmacology For Drug Development - Part 3: Principles of Modeling and Simulation Jul 1, 2015 Online Instruction Global Online
Five-Part Series on Fundamentals of Clinical Pharmacology for Drug Development - Part 4: Determining the Safe First Human Dose Jul 1, 2015 Online Instruction Global Online
Five-Part Series on Fundamentals of Clinical Pharmacology for Drug Development - Part 5: Assessment of QT Prolongation Jul 1, 2015 Online Instruction Global Online
Negotiation and Influence Jul 1, 2015 Online Instruction Global Online
Introduction to Drug Safety Jul 1, 2015 ACPE, IACET Online Instruction Global Online
How to Prepare for a Safety Inspection Jul 1, 2015 Online Instruction Global Online
Implementation and Status of Periodic Benefit-Risk Evaluation Reporting (PBRER) in Canada Jul 1, 2015 Online Instruction Global Online
Clinical Statistics for Nonstatisticians Jul 1, 2015 Online Instruction Global Online
Advanced Clinical Statistics for Nonstatisticians Jul 1, 2015 Online Instruction Global Online
Development of a Clinical Study Report Jul 1, 2015 Online Instruction Global Online
Oversight of Clinical Monitoring: Trends and Strategies Jul 1, 2015 Online Instruction Global Online
Art of Writing a Clinical Overview Jul 1, 2015 Online Instruction Global Online
Seven-Part Series on Pediatric Drug Development - Part 6: Preclinical Toxicology & Safety Jul 1, 2015 Online Instruction Global Online
Complimentary - Need to Reinvent the Clinical Trial? Innovate, Collaborate & Integrate Jul 1, 2015 Online Instruction Global Online
Complimentary Webinar - How to Cut Clinical Trial Timelines in Half Jul 1, 2015 Online Instruction Global Online
Disruptive Innovation in Medical Information Jul 1, 2015 Online Instruction Global Online
A Tour of FDA Jul 1, 2015 Online Instruction Global Online
A Tour of Health Canada Jul 1, 2015 Online Instruction Global Online
A Tour of Health Europe Jul 1, 2015 Online Instruction Global Online
Aspects of Regulatory History Jul 1, 2015 Online Instruction Global Online
Bioresearch Monitoring Program (BIMO): Introduction Jul 1, 2015 Online Instruction Global Online
The Clinical Development Process: Investigational Product, Plan, and Data Management Jul 1, 2015 Online Instruction Global Online
Ethical Review Boards Jul 1, 2015 Online Instruction Global Online
Ethics as the Foundation to Clinical Research Jul 1, 2015 Online Instruction Global Online
Awareness of FDA Inspections for Pharmaceutical Manufacturers Jul 1, 2015 Online Instruction Global Online
Biotechnology: An Overview of Compliance Considerations Jul 1, 2015 Online Instruction Global Online
Change Control Jul 1, 2015 Online Instruction Global Online
Clinical Trial Audits and Consequences of Non-Compliance Jul 1, 2015 Online Instruction Global Online
Computerized Systems Inspections in the Medical Device Industry Jul 1, 2015 Online Instruction Global Online
European Union Clinical Trials Directive Jul 1, 2015 Online Instruction Global Online
GMP Principals of SOPs Jul 1, 2015 Online Instruction Global Online
GMP Updates - Enforcement Changes at the New FDA Jul 1, 2015 Online Instruction Global Online
GMPs for API Bulk Manufacturers Jul 1, 2015 Online Instruction Global Online
Good Clinical Practices (GCPs) for New Product Investigations Jul 1, 2015 Online Instruction Global Online
Good Laboratory Practices (GLPs) Jul 1, 2015 Online Instruction Global Online
GxPs Jul 1, 2015 Online Instruction Global Online
HIPAA - The Impact on Clinical Research Jul 1, 2015 Online Instruction Global Online
Introduction to GMPs Jul 1, 2015 Online Instruction Global Online
Investigational Product Development Jul 1, 2015 Online Instruction Global Online
ISO 14155: Obligations of Sponsors and Monitors for Medical Device Trials Jul 1, 2015 Online Instruction Global Online
Key Concepts of Process Validation Jul 1, 2015 Online Instruction Global Online
Laboratory Specimens for Clinical Research Jul 1, 2015 Online Instruction Global Online
Medical Device Safety Reporting Jul 1, 2015 Online Instruction Global Online
Orientation to GMP Compliance Jul 1, 2015 Online Instruction Global Online
Overview of the Clinical Research Process Jul 1, 2015 Online Instruction Global Online
Part 11: Electronic Records and Signatures - Application Jul 1, 2015 Online Instruction Global Online
Part 11: Electronic Records; Electronic Signatures Jul 1, 2015 Online Instruction Global Online
Principles of Good Documentation Jul 1, 2015 Online Instruction Global Online
Protection of Human Subjects in Clinical Trials Jul 1, 2015 Online Instruction Global Online
Selecting and Managing Clinical Contract Research Organizations (CROs) Jul 1, 2015 Online Instruction Global Online
Understanding Post-Approval Changes Jul 1, 2015 Online Instruction Global Online
Computerized Systems Inspections in the Pharmaceutical Industry Jul 1, 2015 Online Instruction Global Online
Basics of the PhRMA Code Jul 1, 2015 Online Instruction Global Online
Basics of AdvaMed Code Jul 1, 2015 Online Instruction Global Online
Eucomed Guidelines on Interactions with Healthcare Professionals Jul 1, 2015 Online Instruction Global Online
Introduction to Medical Device Health Care Compliance Jul 1, 2015 Online Instruction Global Online
Foreign Corrupt Practices Act Jul 1, 2015 Online Instruction Global Online
Global Anti-bribery Jul 1, 2015 Online Instruction Global Online
Variations to Marketing Authorisation in Europe Jul 1, 2015 Online Instruction Global Online
Registration of Monoclonal Antibodies Jul 1, 2015 Online Instruction Global Online
How to Gain Approval to Market a Generic Medicinal Product in the USA Jul 1, 2015 Online Instruction Global Online
Pharmacokinetics and Pharmacodynamics in Drug Registration Jul 1, 2015 Online Instruction Global Online
Implementing Risk-Based Monitoring: Practical Approaches Jul 1, 2015 Online Instruction Global Online
Complimentary - Innovative Strategies for Developing Safer Cancer Therapies Jul 1, 2015 Online Instruction Global Online
eRegulatory and Intelligence Virtual Conference Archive Jul 1, 2015 Online Instruction Global Online
Complimentary Archive Webinar - Next Generation Feasibility: Better Planning Through Simulation Jul 1, 2015 Online Instruction Global Online
Planning and Managing Your Projects Jul 1, 2015 Online Instruction Global Online
Team Building and Development Jul 1, 2015 Online Instruction Global Online
Preparing a Clinical Trial Budget Jul 1, 2015 Online Instruction Global Online
Overview of Drug Development Jul 1, 2015 IACET, PMI Online Instruction Global Online
Discovery and Preclinical Testing Phases Jul 1, 2015 Online Instruction Global Online
Phase 1 Studies Jul 1, 2015 Online Instruction Global Online
Phase 2 Studies Jul 1, 2015 Online Instruction Global Online
Phase 3 Studies and Regulatory Review Jul 1, 2015 Online Instruction Global Online
Phase 4 and Life Cycle Management Jul 1, 2015 Online Instruction Global Online
Postmarketing Requirements: The Legal Framework, How They Are Issued, Sponsor Obligations, and Challenges to Overcome Jul 1, 2015 Online Instruction Global Online
Introduction to the European Union Institutions and Regulatory Authority Jul 1, 2015 Online Instruction Global Online
Introduction to US Institutions and Regulatory Authority (FDA) Jul 1, 2015 Online Instruction Global Online
Introduction to Japanese Institutions and Regulatory Authorities Jul 1, 2015 Online Instruction Global Online
Overview of the CTD and eCTD Jul 1, 2015 Online Instruction Global Online
Introduction to the International Conference on Harmonisation (ICH) Jul 1, 2015 Online Instruction Global Online
The Regulatory Development of a Drug Jul 1, 2015 Online Instruction Global Online
Basics of Clinical Trials Jul 1, 2015 Online Instruction Global Online
How to Register Medicinal Products through the Centralized Procedure Jul 1, 2015 Online Instruction Global Online
How to Register Medicinal Products through the Mutual Recognition Procedure Jul 1, 2015 Online Instruction Global Online
How to Maintain Marketing Approvals in Europe for Centrally Authorised Products Jul 1, 2015 Online Instruction Global Online
How to Register a New Drug in the USA Jul 1, 2015 Online Instruction Global Online
How to Register Medicinal Products through the Decentralized Procedure Jul 1, 2015 Online Instruction Global Online
Access to Unapproved Drugs through Compassionate Use Jul 1, 2015 Online Instruction Global Online
Regulatory Requirements for the Conduct of Clinical Trials in Europe Jul 1, 2015 Online Instruction Global Online
Orphan Drugs in the USA, European Union, and Japan Jul 1, 2015 Online Instruction Global Online
Regulatory Requirements for the Submission of Investigational New Drug Applications in the USA (INDs) Jul 1, 2015 Online Instruction Global Online
Meeting Opportunities with Regulatory Agencies Jul 1, 2015 Online Instruction Global Online
Complementary - How New Electronic Trial Master File (eTMF) Data Standards Can Enhance Clinical Trial Efficiency and Quality Jul 1, 2015 Online Instruction Global Online
Complimentary - Regulatory Solutions in the Cloud - 10 Questions You Can't Afford NOT to Ask Jul 1, 2015 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 Jul 1, 2015 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 Groups Jul 1, 2015 Online Instruction Global Online
Complimentary - From the Clinic to the CFO: Adaptive Trials and Financial Decision-Making Jul 1, 2015 Online Instruction Global Online
Complimentary - The Affiliate Challenge – How to Improve Compliance and Efficiency when Working with Regional Affiliates Jul 1, 2015 Online Instruction Global Online
Seven-Part Series on Pediatric Drug Development - Part 1: Overall Challenge: The Vision of Better Medicines for Children Jul 1, 2015 Online Instruction Global Online
Seven-Part Series on Pediatric Drug Development - Part 3: Regulatory Framework EU Jul 1, 2015 Online Instruction Global Online
Seven-Part Pediatric Drug Development Webinar Series - Part 4: Dosing in Children Jul 1, 2015 Online Instruction Global Online
Seven-Part Series on Pediatric Drug Development - Part 2: Regulatory Framework US Overview Jul 1, 2015 Online Instruction Global Online
Seven-Part Series on Pediatric Drug Development - Part 5: Technical Development: Pediatric Formulations Jul 1, 2015 Online Instruction Global Online
Basics of the NDA Phase Jul 1, 2015 Online Instruction Global Online
Regulatory Aspects of Prescription Drug/Biologics Advertising and Promotional Labeling Jul 1, 2015 Online Instruction Global Online
Basics of the IND Phase Jul 1, 2015 Online Instruction Global Online
Seven-Part Series on Pediatric Drug Development - Part 7: Operational Challenges of Pediatric Clinical Trials Jul 1, 2015 Online Instruction Global Online
Clinical Trials Transparency 3 Part Webinar Series - Part 3: Understanding the Legislation Landscape: Regulatory Updates from the FDA, EMA and Health Canada Jul 1, 2015 Online Instruction Global Online
Adverse Event Reporting Requirements: IND and Post-marketing Jul 13, 2015 IACET Online Instruction Global Online
Interactions with the FDA during IND/NDA Phases Jul 16, 2015 IACET Online Instruction Global Online
Global Regulatory Strategy and Drug Development in Asia-Pacific, Latin America, and Other Emerging Markets Aug 3, 2015 In-Person Instruction North America Washington, DC, United States
Development of a Clinical Study Report Aug 10, 2015 IACET In-Person Instruction North America Boston, MA, United States
Regulatory Affairs: The IND, NDA, and Postmarketing Aug 10, 2015 IACET In-Person Instruction North America Boston, MA, United States
Pragmatic Approaches to Drug Safety Across the Premarketing and Postmarketing Continuum Aug 10, 2015 ACPE, IACET In-Person Instruction North America Boston, MA, United States
European Regulatory Affairs: Keeping Your Finger on the Pulse of Marketing Authorizations Aug 11, 2015 In-Person Instruction North America Boston, MA, United States
Clinical Project Management Aug 24, 2015 IACET, PMI In-Person Instruction North America Washington, DC, United States
New Drug Product Development and Life Cycle Management Aug 26, 2015 IACET, PMI In-Person Instruction North America Washington, DC, United States
Overview of Drug Development in Japan Sep 2, 2015 Online Instruction Global Online
DIA/FDA Oligonucleotide-Based Therapeutic Conference 2015 Sep 9, 2015 Meetings North America Washington, DC, United States
Part 1: FDA Initiatives to Meet the Medical Needs of Pregnant and Lactating Women through Improved Labeling of Medical Products Sep 15, 2015 Online Instruction Global Online
Patient Engagement in Benefit-Risk Assessment throughout the Life Cycle of Medical Products Sep 17, 2015 Meetings North America North Bethesda, MD, United States
Clinical Trial Disclosure & Data Transparency – The Expanding Global Environment Sep 17, 2015 Meetings North America Bethesda, MD, United States
Adaptive Design in Clinical Trials: When and How to Apply Sep 21, 2015 IACET In-Person Instruction North America Washington, DC, United States
Drug and Device Combination Products 2015: Navigating Regulation, Enhancing Collaboration, and Accelerating Development Sep 28, 2015 Meetings North America Bethesda, MD, United States
Pragmatic Approaches to Drug Safety Across the Premarketing and Postmarketing Continuum Sep 28, 2015 ACPE, IACET In-Person Instruction North America Toronto, ON, Canada
Clinical Statistics for Nonstatisticians Sep 28, 2015 ACPE, IACET In-Person Instruction North America Washington, DC, United States
Companion Diagnostics Sep 30, 2015 Meetings North America Bethesda, MD, United States
Central Audit Methods for Site Image Interpretation in Clinical Trials Oct 1, 2015 Meetings North America North Bethesda, MD, United States
Study Endpoints Oct 5, 2015 Meetings North America Bethesda, MD, United States
Introduction to Signal Detection and Data Mining Oct 5, 2015 IACET Online Instruction Global Online
Achieving Meaningful Regulatory and Clinical Outcomes for Patients: Strategies in Rare Disease Therapy Development Oct 7, 2015 Meetings North America Bethesda, MD, United States
Part 2: Overcoming the Challenges of Conducting Postmarketing Studies in Pregnant and Lactating Women Oct 13, 2015 Online Instruction Global Online
Clinical Statistics for Nonstatisticians Oct 14, 2015 ACPE, IACET In-Person Instruction North America Durham, NC, United States
Tutorial 1: Achieving Biosimilarity Through Matching of Critical Quality Attributes to Reference Product’s Oct 18, 2015 In-Person Instruction North America Bethesda, MD, United States
Biosimilars 2015 Oct 19, 2015 Meetings North America Bethesda, MD, United States
Risk Management and Safety Communication Oct 26, 2015 ACPE, IACET In-Person Instruction North America Washington, DC, United States
DIA Annual Canadian Meeting 2015 Oct 27, 2015 Meetings North America Ottawa, ON, Canada
Postmarketing Drug Safety & Pharmacovigilance Nov 9, 2015 ACPE, IACET In-Person Instruction North America Philadelphia, PA, United States
Regulatory Affairs: The IND, NDA, and Postmarketing Nov 9, 2015 IACET In-Person Instruction North America Philadelphia, PA, United States
Navigating Chemistry, Manufacturing and Controls Through the Drug Development Process Nov 9, 2015 IACET In-Person Instruction North America Philadelphia, PA, United States
Part 3: Assessing the Safety of Medications and Vaccines in Pregnancy: The Vaccines and Medications in Pregnancy Surveillance System Nov 10, 2015 Online Instruction Global Online
Advanced Clinical Statistics for NonStatisticians Nov 11, 2015 ACPE, IACET In-Person Instruction North America Philadelphia, PA, United States
Part 4: CDC’s Treating for Two Initiative and Other Federal Efforts to Disseminate Data for Informed Clinical Decision Making in Pregnancy and Lactation Dec 8, 2015 Online Instruction Global Online
Pharmacovigilance and Risk Management Strategies 2016 Jan 25, 2016 Meetings North America
Medical and Scientific Communications 2016 Annual Forum Mar 21, 2016 Meetings North America Kissimmee, FL, United States
DIA/FDA Statistics 2016 Forum Apr 25, 2016 Meetings North America North Bethesda, MD, United States
DIA 2016 52nd Annual Meeting Jun 26, 2016 Meetings North America Philadelphia, PA, United States