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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
The Use of Mobile Medical Applications as Companions Dec 22, 2014 Online Instruction Global Online
Generic Drug Labeling Proposed Rule and Safety Updates Dec 22, 2014 Online Instruction Global Online
Emerging Technologies to Rare Disorder Drug Development: Promises and Pitfalls Dec 22, 2014 Online Instruction Global Online
Target Product Profile – Strategies to Optimize Drug Development, Product Labeling, and Commercialization Dec 22, 2014 Online Instruction Global Online
The Role of the Clinical Data Manager Dec 22, 2014 Online Instruction Global Online
Implementation of the FDASIA Patient Provisions Dec 22, 2014 Online Instruction Global Online
Complimentary: Regulatory and Real World Evidence Challenges of Rare Diseases and Orphan Drugs Dec 22, 2014 Online Instruction Global Online
Variations in the European Union: CMC/Quality Changes Dec 22, 2014 Online Instruction Global Online
Proarrhythmia Dec 22, 2014 Online Instruction Global Online
Facets of Drug-Induced Kidney Injury and Regulatory Perspective Dec 22, 2014 Online Instruction Global Online
Impact on Drug Development of Novel Translational Safety Biomarkers for Improved Detection of Drug-Induced Acute Kidney Injury Dec 22, 2014 Online Instruction Global Online
Pharmacovigilance and Risk Management: Patient Perspective Dec 22, 2014 Online Instruction Global Online
Complimentary Patient-Centeredness and Engagement in Clinical Research: Opportunities for Industry Dec 22, 2014 Online Instruction Global Online
Drug Safety Regulatory Requirements Dec 22, 2014 ACPE, IACET Online Instruction Global Online
Premarketing Clinical Trial Safety Dec 22, 2014 ACPE, IACET Online Instruction Global Online
Postmarketing Safety Management Dec 22, 2014 ACPE, IACET Online Instruction Global Online
Basics of Signal Detection and Pharmacoepidemiology Dec 22, 2014 ACPE, IACET Online Instruction Global Online
Safety Audits and Inspections Dec 22, 2014 ACPE, IACET Online Instruction Global Online
Five-Part Series on Fundamentals of Clinical Pharmacology for Drug Development - Part 1: Fundamentals of Clinical Pharmacology: Pharmacokinetics Dec 22, 2014 Online Instruction Global Online
Five-Part Series on Fundamentals of Clinical Pharmacology for Drug Development - Part 2: Fundamentals of Clinical Pharmacology: Pharmacodynamics Dec 22, 2014 Online Instruction Global Online
Pharmacovigilance and Global Harmonization Updates Dec 22, 2014 Online Instruction Global Online
Five-Part Series on Fundamentals of Clinical Pharmacology For Drug Development - Part 3: Principles of Modeling and Simulation Dec 22, 2014 Online Instruction Global Online
Five-Part Series on Fundamentals of Clinical Pharmacology for Drug Development - Part 4: Determining the Safe First Human Dose Dec 22, 2014 Online Instruction Global Online
Five-Part Series on Fundamentals of Clinical Pharmacology for Drug Development - Part 5: Assessment of QT Prolongation Dec 22, 2014 Online Instruction Global Online
Designed for Success: Utilizing Protocol Quality by Design (QbD) to Plan Clinical Studies Dec 22, 2014 Online Instruction Global Online
Negotiation and Influence Dec 22, 2014 Online Instruction Global Online
Introduction to Drug Safety Dec 22, 2014 ACPE, IACET Online Instruction Global Online
How to Prepare for a Safety Inspection Dec 22, 2014 Online Instruction Global Online
Implementation and Status of Periodic Benefit-Risk Evaluation Reporting (PBRER) in Canada Dec 22, 2014 Online Instruction Global Online
Clinical Statistics for Nonstatisticians Dec 22, 2014 Online Instruction Global Online
Advanced Clinical Statistics for Nonstatisticians Dec 22, 2014 Online Instruction Global Online
Development of a Clinical Study Report Dec 22, 2014 Online Instruction Global Online
Art of Writing a Clinical Overview Dec 22, 2014 Online Instruction Global Online
Introductory Principles and Application of Risk Management within Clinical Operations Dec 22, 2014 Online Instruction Global Online
Seven-Part Series on Pediatric Drug Development - Part 6: Preclinical Toxicology & Safety Dec 22, 2014 Online Instruction Global Online
Complimentary - Need to Reinvent the Clinical Trial? Innovate, Collaborate & Integrate Dec 22, 2014 Online Instruction Global Online
Disruptive Innovation in Medical Information Dec 22, 2014 Online Instruction Global Online
A Tour of FDA Dec 22, 2014 Online Instruction Global Online
A Tour of Health Canada Dec 22, 2014 Online Instruction Global Online
A Tour of Health Europe Dec 22, 2014 Online Instruction Global Online
Aspects of Regulatory History Dec 22, 2014 Online Instruction Global Online
Bioresearch Monitoring Program (BIMO): Introduction Dec 22, 2014 Online Instruction Global Online
The Clinical Development Process: Investigational Product, Plan, and Data Management Dec 22, 2014 Online Instruction Global Online
Drug Safety & Adverse Event Reporting Dec 22, 2014 Online Instruction Global Online
Ethical Review Boards Dec 22, 2014 Online Instruction Global Online
Ethics as the Foundation to Clinical Research Dec 22, 2014 Online Instruction Global Online
Awareness of FDA Inspections for Pharmaceutical Manufacturers Dec 22, 2014 Online Instruction Global Online
Biotechnology: An Overview of Compliance Considerations Dec 22, 2014 Online Instruction Global Online
Change Control Dec 22, 2014 Online Instruction Global Online
Clinical Trial Audits and Consequences of Non-Compliance Dec 22, 2014 Online Instruction Global Online
Computerized Systems Inspections in the Medical Device Industry Dec 22, 2014 Online Instruction Global Online
European Union Clinical Trials Directive Dec 22, 2014 Online Instruction Global Online
GMP Principals of SOPs Dec 22, 2014 Online Instruction Global Online
GMP Updates - Enforcement Changes at the New FDA Dec 22, 2014 Online Instruction Global Online
GMPs for API Bulk Manufacturers Dec 22, 2014 Online Instruction Global Online
Good Clinical Practices (GCPs) for New Product Investigations Dec 22, 2014 Online Instruction Global Online
Good Laboratory Practices (GLPs) Dec 22, 2014 Online Instruction Global Online
GxPs Dec 22, 2014 Online Instruction Global Online
HIPAA - The Impact on Clinical Research Dec 22, 2014 Online Instruction Global Online
Introduction to GMPs Dec 22, 2014 Online Instruction Global Online
Investigational Product Development Dec 22, 2014 Online Instruction Global Online
ISO 14155: Obligations of Sponsors and Monitors for Medical Device Trials Dec 22, 2014 Online Instruction Global Online
Key Concepts of Process Validation Dec 22, 2014 Online Instruction Global Online
Laboratory Specimens for Clinical Research Dec 22, 2014 Online Instruction Global Online
Medical Device Safety Reporting Dec 22, 2014 Online Instruction Global Online
Orientation to GMP Compliance Dec 22, 2014 Online Instruction Global Online
Overview of the Clinical Research Process Dec 22, 2014 Online Instruction Global Online
Part 11: Electronic Records and Signatures - Application Dec 22, 2014 Online Instruction Global Online
Part 11: Electronic Records; Electronic Signatures Dec 22, 2014 Online Instruction Global Online
Principles of Good Documentation Dec 22, 2014 Online Instruction Global Online
Protection of Human Subjects in Clinical Trials Dec 22, 2014 Online Instruction Global Online
Selecting and Managing Clinical Contract Research Organizations (CROs) Dec 22, 2014 Online Instruction Global Online
Understanding Post-Approval Changes Dec 22, 2014 Online Instruction Global Online
Computerized Systems Inspections in the Pharmaceutical Industry Dec 22, 2014 Online Instruction Global Online
Basics of the PhRMA Code Dec 22, 2014 Online Instruction Global Online
Basics of AdvaMed Code Dec 22, 2014 Online Instruction Global Online
Eucomed Guidelines on Interactions with Healthcare Professionals Dec 22, 2014 Online Instruction Global Online
Introduction to Medical Device Health Care Compliance Dec 22, 2014 Online Instruction Global Online
Foreign Corrupt Practices Act Dec 22, 2014 Online Instruction Global Online
Global Anti-bribery Dec 22, 2014 Online Instruction Global Online
Variations to Marketing Authorisation in Europe Dec 22, 2014 Online Instruction Global Online
Registration of Monoclonal Antibodies Dec 22, 2014 Online Instruction Global Online
How to Gain Approval to Market a Generic Medicinal Product in the USA Dec 22, 2014 Online Instruction Global Online
Pharmacokinetics and Pharmacodynamics in Drug Registration Dec 22, 2014 Online Instruction Global Online
Complimentary Quintiles/DIA Webinar - Giving Your Study The Right Start Toward Success Through Optimal Country and Site Selection Dec 22, 2014 Online Instruction Global Online
Implementing Risk-Based Monitoring: Practical Approaches Dec 22, 2014 Online Instruction Global Online
Complimentary - Innovative Strategies for Developing Safer Cancer Therapies Dec 22, 2014 Online Instruction Global Online
Complimentary - Risk-Based Monitoring: Regulatory Expectation and Operational Application Dec 22, 2014 Online Instruction Global Online
Fundamentals of Project Management for Nonproject Managers Dec 22, 2014 Online Instruction Global Online
Planning and Managing Your Projects Dec 22, 2014 Online Instruction Global Online
Preparing a Clinical Trial Budget Dec 22, 2014 Online Instruction Global Online
Team Building and Development Dec 22, 2014 Online Instruction Global Online
Introduction to the European Union Institutions and Regulatory Authority Dec 22, 2014 Online Instruction Global Online
Introduction to US Institutions and Regulatory Authority (FDA) Dec 22, 2014 Online Instruction Global Online
Introduction to Japanese Institutions and Regulatory Authorities Dec 22, 2014 Online Instruction Global Online
Overview of the CTD and eCTD Dec 22, 2014 Online Instruction Global Online
Introduction to the International Conference on Harmonisation (ICH) Dec 22, 2014 Online Instruction Global Online
The Regulatory Development of a Drug Dec 22, 2014 Online Instruction Global Online
Basics of Clinical Trials Dec 22, 2014 Online Instruction Global Online
How to Register Medicinal Products through the Centralized Procedure Dec 22, 2014 Online Instruction Global Online
How to Register Medicinal Products through the Mutual Recognition Procedure Dec 22, 2014 Online Instruction Global Online
How to Maintain Marketing Approvals in Europe for Centrally Authorised Products Dec 22, 2014 Online Instruction Global Online
How to Register a New Drug in the USA Dec 22, 2014 Online Instruction Global Online
How to Register Medicinal Products through the Decentralized Procedure Dec 22, 2014 Online Instruction Global Online
Access to Unapproved Drugs through Compassionate Use Dec 22, 2014 Online Instruction Global Online
Regulatory Requirements for the Conduct of Clinical Trials in Europe Dec 22, 2014 Online Instruction Global Online
Orphan Drugs in the USA, European Union, and Japan Dec 22, 2014 Online Instruction Global Online
Regulatory Requirements for the Submission of Investigational New Drug Applications in the USA (INDs) Dec 22, 2014 Online Instruction Global Online
Meeting Opportunities with Regulatory Agencies Dec 22, 2014 Online Instruction Global Online
How New Electronic Trial Master File (eTMF) Data Standards Can Enhance Clinical Trial Efficiency and Quality Dec 22, 2014 Online Instruction Global Online
Complimentary - Regulatory Solutions in the Cloud - 10 Questions You Can't Afford NOT to Ask Dec 22, 2014 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 Dec 22, 2014 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 Dec 22, 2014 Online Instruction Global Online
Complimentary - From the Clinic to the CFO: Adaptive Trials and Financial Decision-Making Dec 22, 2014 Online Instruction Global Online
Adverse Event Reporting Requirements: IND and Postmarketing Dec 22, 2014 Online Instruction Global Online
Complimentary - The Affiliate Challenge – How to Improve Compliance and Efficiency when Working with Regional Affiliates Dec 22, 2014 Online Instruction Global Online
The Future of Personalized Medicine and Companion Diagnostics Dec 22, 2014 Online Instruction Global Online
Seven-Part Series on Pediatric Drug Development - Part 1: Overall Challenge: The Vision of Better Medicines for Children Dec 22, 2014 Online Instruction Global Online
Seven-Part Series on Pediatric Drug Development - Part 3: Regulatory Framework EU Dec 22, 2014 Online Instruction Global Online
Seven-Part Pediatric Drug Development Webinar Series - Part 4: Dosing in Children Dec 22, 2014 Online Instruction Global Online
Seven-Part Series on Pediatric Drug Development - Part 2: Regulatory Framework US Overview Dec 22, 2014 Online Instruction Global Online
Seven-Part Series on Pediatric Drug Development - Part 5: Technical Development: Pediatric Formulations Dec 22, 2014 Online Instruction Global Online
Basics of the IND Dec 22, 2014 Online Instruction Global Online
Basics of the NDA Dec 22, 2014 Online Instruction Global Online
Regulatory Aspects of Prescription Drug/Biologics Advertising and Promotional Labeling Dec 22, 2014 Online Instruction Global Online
Seven-Part Series on Pediatric Drug Development - Part 7: Operational Challenges of Pediatric Clinical Trials Dec 22, 2014 Online Instruction Global Online
Supplements and Other Changes to an Approved Application Dec 22, 2014 Online Instruction Global Online
Regulatory Aspects of Prescription Drug/Biologics Advertising and Promotional Labeling Feb 05, 2015 IACET Online Instruction Global Online
Art of Writing a Clinical Overview Feb 24, 2015 IACET Online Instruction Global Online
Preparing a Clinical Trial Budget Mar 10, 2015 Online Instruction Global Online
Basics of the IND Phase May 04, 2015 Online Instruction Global Online
Oversight of Clinical Monitoring: Trends and Strategies May 05, 2015 Online Instruction Global Online
Basics of the NDA Phase May 18, 2015 Online Instruction Global Online
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 Online Instruction Global Online