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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
Expert Reactor Panel: IOM Report on Sharing Clinical Trial Data Mar 31, 2015 Online Instruction Global Online
Novel Data Sources: The Positive Impact of Social Media and Online Networks for Engaging with Patients Mar 31, 2015 Online Instruction Global Online
Generic Drug Labeling Proposed Rule and Safety Updates Mar 31, 2015 Online Instruction Global Online
FDA’s Evolving Position on the Brief Summary Mar 31, 2015 Online Instruction Global Online
Target Product Profile – Strategies to Optimize Drug Development, Product Labeling, and Commercialization Mar 31, 2015 Online Instruction Global Online
GVP Module IX Compliant Signal Management Systems in Pharmacovigilance: A Tale of Two Experiences Mar 31, 2015 Online Instruction Global Online
The Role of the Clinical Data Manager Mar 31, 2015 Online Instruction Global Online
Implementation of the FDASIA Patient Provisions Mar 31, 2015 Online Instruction Global Online
Complimentary: Regulatory and Real World Evidence Challenges of Rare Diseases and Orphan Drugs Mar 31, 2015 Online Instruction Global Online
Variations in the European Union: CMC/Quality Changes Mar 31, 2015 Online Instruction Global Online
Proarrhythmia Mar 31, 2015 Online Instruction Global Online
Facets of Drug-Induced Kidney Injury and Regulatory Perspective Mar 31, 2015 Online Instruction Global Online
Impact on Drug Development of Novel Translational Safety Biomarkers for Improved Detection of Drug-Induced Acute Kidney Injury Mar 31, 2015 Online Instruction Global Online
Pharmacovigilance and Risk Management: Patient Perspective Mar 31, 2015 Online Instruction Global Online
Drug Safety Regulatory Requirements Mar 31, 2015 ACPE, IACET Online Instruction Global Online
Premarketing Clinical Trial Safety Mar 31, 2015 ACPE, IACET Online Instruction Global Online
Postmarketing Safety Management Mar 31, 2015 ACPE, IACET Online Instruction Global Online
Basics of Signal Detection and Pharmacoepidemiology Mar 31, 2015 ACPE, IACET Online Instruction Global Online
Safety Audits and Inspections Mar 31, 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 Mar 31, 2015 Online Instruction Global Online
Five-Part Series on Fundamentals of Clinical Pharmacology for Drug Development - Part 2: Fundamentals of Clinical Pharmacology: Pharmacodynamics Mar 31, 2015 Online Instruction Global Online
Pharmacovigilance and Global Harmonization Updates Mar 31, 2015 Online Instruction Global Online
Five-Part Series on Fundamentals of Clinical Pharmacology For Drug Development - Part 3: Principles of Modeling and Simulation Mar 31, 2015 Online Instruction Global Online
Five-Part Series on Fundamentals of Clinical Pharmacology for Drug Development - Part 4: Determining the Safe First Human Dose Mar 31, 2015 Online Instruction Global Online
Five-Part Series on Fundamentals of Clinical Pharmacology for Drug Development - Part 5: Assessment of QT Prolongation Mar 31, 2015 Online Instruction Global Online
Designed for Success: Utilizing Protocol Quality by Design (QbD) to Plan Clinical Studies Mar 31, 2015 Online Instruction Global Online
Negotiation and Influence Mar 31, 2015 Online Instruction Global Online
Introduction to Drug Safety Mar 31, 2015 ACPE, IACET Online Instruction Global Online
How to Prepare for a Safety Inspection Mar 31, 2015 Online Instruction Global Online
Implementation and Status of Periodic Benefit-Risk Evaluation Reporting (PBRER) in Canada Mar 31, 2015 Online Instruction Global Online
Clinical Statistics for Nonstatisticians Mar 31, 2015 Online Instruction Global Online
Advanced Clinical Statistics for Nonstatisticians Mar 31, 2015 Online Instruction Global Online
Development of a Clinical Study Report Mar 31, 2015 Online Instruction Global Online
Art of Writing a Clinical Overview Mar 31, 2015 Online Instruction Global Online
Seven-Part Series on Pediatric Drug Development - Part 6: Preclinical Toxicology & Safety Mar 31, 2015 Online Instruction Global Online
Complimentary - Need to Reinvent the Clinical Trial? Innovate, Collaborate & Integrate Mar 31, 2015 Online Instruction Global Online
Complimentary Webinar - How to Cut Clinical Trial Timelines in Half Mar 31, 2015 Online Instruction Global Online
Disruptive Innovation in Medical Information Mar 31, 2015 Online Instruction Global Online
A Tour of FDA Mar 31, 2015 Online Instruction Global Online
A Tour of Health Canada Mar 31, 2015 Online Instruction Global Online
A Tour of Health Europe Mar 31, 2015 Online Instruction Global Online
Aspects of Regulatory History Mar 31, 2015 Online Instruction Global Online
Bioresearch Monitoring Program (BIMO): Introduction Mar 31, 2015 Online Instruction Global Online
The Clinical Development Process: Investigational Product, Plan, and Data Management Mar 31, 2015 Online Instruction Global Online
Ethical Review Boards Mar 31, 2015 Online Instruction Global Online
Ethics as the Foundation to Clinical Research Mar 31, 2015 Online Instruction Global Online
Awareness of FDA Inspections for Pharmaceutical Manufacturers Mar 31, 2015 Online Instruction Global Online
Biotechnology: An Overview of Compliance Considerations Mar 31, 2015 Online Instruction Global Online
Change Control Mar 31, 2015 Online Instruction Global Online
Clinical Trial Audits and Consequences of Non-Compliance Mar 31, 2015 Online Instruction Global Online
Computerized Systems Inspections in the Medical Device Industry Mar 31, 2015 Online Instruction Global Online
European Union Clinical Trials Directive Mar 31, 2015 Online Instruction Global Online
GMP Principals of SOPs Mar 31, 2015 Online Instruction Global Online
GMP Updates - Enforcement Changes at the New FDA Mar 31, 2015 Online Instruction Global Online
GMPs for API Bulk Manufacturers Mar 31, 2015 Online Instruction Global Online
Good Clinical Practices (GCPs) for New Product Investigations Mar 31, 2015 Online Instruction Global Online
Good Laboratory Practices (GLPs) Mar 31, 2015 Online Instruction Global Online
GxPs Mar 31, 2015 Online Instruction Global Online
HIPAA - The Impact on Clinical Research Mar 31, 2015 Online Instruction Global Online
Introduction to GMPs Mar 31, 2015 Online Instruction Global Online
Investigational Product Development Mar 31, 2015 Online Instruction Global Online
ISO 14155: Obligations of Sponsors and Monitors for Medical Device Trials Mar 31, 2015 Online Instruction Global Online
Key Concepts of Process Validation Mar 31, 2015 Online Instruction Global Online
Laboratory Specimens for Clinical Research Mar 31, 2015 Online Instruction Global Online
Medical Device Safety Reporting Mar 31, 2015 Online Instruction Global Online
Orientation to GMP Compliance Mar 31, 2015 Online Instruction Global Online
Overview of the Clinical Research Process Mar 31, 2015 Online Instruction Global Online
Part 11: Electronic Records and Signatures - Application Mar 31, 2015 Online Instruction Global Online
Part 11: Electronic Records; Electronic Signatures Mar 31, 2015 Online Instruction Global Online
Principles of Good Documentation Mar 31, 2015 Online Instruction Global Online
Protection of Human Subjects in Clinical Trials Mar 31, 2015 Online Instruction Global Online
Selecting and Managing Clinical Contract Research Organizations (CROs) Mar 31, 2015 Online Instruction Global Online
Understanding Post-Approval Changes Mar 31, 2015 Online Instruction Global Online
Computerized Systems Inspections in the Pharmaceutical Industry Mar 31, 2015 Online Instruction Global Online
Basics of the PhRMA Code Mar 31, 2015 Online Instruction Global Online
Basics of AdvaMed Code Mar 31, 2015 Online Instruction Global Online
Eucomed Guidelines on Interactions with Healthcare Professionals Mar 31, 2015 Online Instruction Global Online
Introduction to Medical Device Health Care Compliance Mar 31, 2015 Online Instruction Global Online
Foreign Corrupt Practices Act Mar 31, 2015 Online Instruction Global Online
Global Anti-bribery Mar 31, 2015 Online Instruction Global Online
Variations to Marketing Authorisation in Europe Mar 31, 2015 Online Instruction Global Online
Registration of Monoclonal Antibodies Mar 31, 2015 Online Instruction Global Online
How to Gain Approval to Market a Generic Medicinal Product in the USA Mar 31, 2015 Online Instruction Global Online
Pharmacokinetics and Pharmacodynamics in Drug Registration Mar 31, 2015 Online Instruction Global Online
Implementing Risk-Based Monitoring: Practical Approaches Mar 31, 2015 Online Instruction Global Online
Complimentary - Innovative Strategies for Developing Safer Cancer Therapies Mar 31, 2015 Online Instruction Global Online
Complimentary - Risk-Based Monitoring: Regulatory Expectation and Operational Application Mar 31, 2015 Online Instruction Global Online
Fundamentals of Project Management for Nonproject Managers Mar 31, 2015 Online Instruction Global Online
Planning and Managing Your Projects Mar 31, 2015 Online Instruction Global Online
Team Building and Development Mar 31, 2015 Online Instruction Global Online
Preparing a Clinical Trial Budget Mar 31, 2015 Online Instruction Global Online
Introduction to the European Union Institutions and Regulatory Authority Mar 31, 2015 Online Instruction Global Online
Introduction to US Institutions and Regulatory Authority (FDA) Mar 31, 2015 Online Instruction Global Online
Introduction to Japanese Institutions and Regulatory Authorities Mar 31, 2015 Online Instruction Global Online
Overview of the CTD and eCTD Mar 31, 2015 Online Instruction Global Online
Introduction to the International Conference on Harmonisation (ICH) Mar 31, 2015 Online Instruction Global Online
The Regulatory Development of a Drug Mar 31, 2015 Online Instruction Global Online
Basics of Clinical Trials Mar 31, 2015 Online Instruction Global Online
How to Register Medicinal Products through the Centralized Procedure Mar 31, 2015 Online Instruction Global Online
How to Register Medicinal Products through the Mutual Recognition Procedure Mar 31, 2015 Online Instruction Global Online
How to Maintain Marketing Approvals in Europe for Centrally Authorised Products Mar 31, 2015 Online Instruction Global Online
How to Register a New Drug in the USA Mar 31, 2015 Online Instruction Global Online
How to Register Medicinal Products through the Decentralized Procedure Mar 31, 2015 Online Instruction Global Online
Access to Unapproved Drugs through Compassionate Use Mar 31, 2015 Online Instruction Global Online
Regulatory Requirements for the Conduct of Clinical Trials in Europe Mar 31, 2015 Online Instruction Global Online
Orphan Drugs in the USA, European Union, and Japan Mar 31, 2015 Online Instruction Global Online
Regulatory Requirements for the Submission of Investigational New Drug Applications in the USA (INDs) Mar 31, 2015 Online Instruction Global Online
Meeting Opportunities with Regulatory Agencies Mar 31, 2015 Online Instruction Global Online
Complementary - How New Electronic Trial Master File (eTMF) Data Standards Can Enhance Clinical Trial Efficiency and Quality Mar 31, 2015 Online Instruction Global Online
Complimentary - Regulatory Solutions in the Cloud - 10 Questions You Can't Afford NOT to Ask Mar 31, 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 Mar 31, 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 Mar 31, 2015 Online Instruction Global Online
Complimentary - From the Clinic to the CFO: Adaptive Trials and Financial Decision-Making Mar 31, 2015 Online Instruction Global Online
Adverse Event Reporting Requirements: IND and Postmarketing Mar 31, 2015 Online Instruction Global Online
Complimentary - The Affiliate Challenge – How to Improve Compliance and Efficiency when Working with Regional Affiliates Mar 31, 2015 Online Instruction Global Online
Seven-Part Series on Pediatric Drug Development - Part 1: Overall Challenge: The Vision of Better Medicines for Children Mar 31, 2015 Online Instruction Global Online
Seven-Part Series on Pediatric Drug Development - Part 3: Regulatory Framework EU Mar 31, 2015 Online Instruction Global Online
Seven-Part Pediatric Drug Development Webinar Series - Part 4: Dosing in Children Mar 31, 2015 Online Instruction Global Online
Seven-Part Series on Pediatric Drug Development - Part 2: Regulatory Framework US Overview Mar 31, 2015 Online Instruction Global Online
Seven-Part Series on Pediatric Drug Development - Part 5: Technical Development: Pediatric Formulations Mar 31, 2015 Online Instruction Global Online
Basics of the IND Mar 31, 2015 Online Instruction Global Online
Basics of the NDA Mar 31, 2015 Online Instruction Global Online
Regulatory Aspects of Prescription Drug/Biologics Advertising and Promotional Labeling Mar 31, 2015 Online Instruction Global Online
Seven-Part Series on Pediatric Drug Development - Part 7: Operational Challenges of Pediatric Clinical Trials Mar 31, 2015 Online Instruction Global Online
Supplements and Other Changes to an Approved Application Mar 31, 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 Mar 31, 2015 Online Instruction Global Online
GVP Module IX Compliant Signal Management Systems in Pharmacovigilance: A Tale of Two Experiences Apr 02, 2015 ACPE, IACET Online Instruction Global Online
Complimentary Webinar - Using Revolutionary Machine Learning to Find the Most Relevant Content to Drive Informed Decisions in Regulatory Intelligence Apr 08, 2015 Online Instruction Global Online
Key Considerations for Biosimilar R&D Workshop Apr 27, 2015 Meetings China
FDA’s Evolving Position on the Brief Summary Apr 28, 2015 IACET Online Instruction Global Online
Basics of the IND Phase May 04, 2015 IACET Online Instruction Global Online
Oversight of Clinical Monitoring: Trends and Strategies May 05, 2015 IACET Online Instruction Global Online
eRegulatory and Intelligence Virtual Conference May 11, 2015 Meetings Global
Basics of the NDA Phase May 18, 2015 IACET Online Instruction Global Online
The 7th DIA China Annual Meeting May 24, 2015 Meetings China Shanghai, China
How to Prepare for a Safety Inspection Jun 01, 2015 IACET Online Instruction Global Online
Adverse Event Reporting Requirements: IND and Post-marketing Jul 13, 2015 Online Instruction Global Online
Interactions with the FDA during IND/NDA Phases Jul 16, 2015 Online Instruction Global Online
Overview of Drug Development in Japan Sep 02, 2015 Online Instruction Global Online
Introduction to Signal Detection and Data Mining Oct 05, 2015 IACET Online Instruction Global Online