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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 Jan 29, 2015 Online Instruction Global Online
Generic Drug Labeling Proposed Rule and Safety Updates Jan 29, 2015 Online Instruction Global Online
Emerging Technologies to Rare Disorder Drug Development: Promises and Pitfalls Jan 29, 2015 Online Instruction Global Online
Target Product Profile – Strategies to Optimize Drug Development, Product Labeling, and Commercialization Jan 29, 2015 Online Instruction Global Online
The Role of the Clinical Data Manager Jan 29, 2015 Online Instruction Global Online
Implementation of the FDASIA Patient Provisions Jan 29, 2015 Online Instruction Global Online
Complimentary: Regulatory and Real World Evidence Challenges of Rare Diseases and Orphan Drugs Jan 29, 2015 Online Instruction Global Online
Variations in the European Union: CMC/Quality Changes Jan 29, 2015 Online Instruction Global Online
Proarrhythmia Jan 29, 2015 Online Instruction Global Online
Facets of Drug-Induced Kidney Injury and Regulatory Perspective Jan 29, 2015 Online Instruction Global Online
Impact on Drug Development of Novel Translational Safety Biomarkers for Improved Detection of Drug-Induced Acute Kidney Injury Jan 29, 2015 Online Instruction Global Online
Pharmacovigilance and Risk Management: Patient Perspective Jan 29, 2015 Online Instruction Global Online
Complimentary Patient-Centeredness and Engagement in Clinical Research: Opportunities for Industry Jan 29, 2015 Online Instruction Global Online
Drug Safety Regulatory Requirements Jan 29, 2015 ACPE, IACET Online Instruction Global Online
Premarketing Clinical Trial Safety Jan 29, 2015 ACPE, IACET Online Instruction Global Online
Postmarketing Safety Management Jan 29, 2015 ACPE, IACET Online Instruction Global Online
Basics of Signal Detection and Pharmacoepidemiology Jan 29, 2015 ACPE, IACET Online Instruction Global Online
Safety Audits and Inspections Jan 29, 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 Jan 29, 2015 Online Instruction Global Online
Five-Part Series on Fundamentals of Clinical Pharmacology for Drug Development - Part 2: Fundamentals of Clinical Pharmacology: Pharmacodynamics Jan 29, 2015 Online Instruction Global Online
Pharmacovigilance and Global Harmonization Updates Jan 29, 2015 Online Instruction Global Online
Five-Part Series on Fundamentals of Clinical Pharmacology For Drug Development - Part 3: Principles of Modeling and Simulation Jan 29, 2015 Online Instruction Global Online
Five-Part Series on Fundamentals of Clinical Pharmacology for Drug Development - Part 4: Determining the Safe First Human Dose Jan 29, 2015 Online Instruction Global Online
Five-Part Series on Fundamentals of Clinical Pharmacology for Drug Development - Part 5: Assessment of QT Prolongation Jan 29, 2015 Online Instruction Global Online
Designed for Success: Utilizing Protocol Quality by Design (QbD) to Plan Clinical Studies Jan 29, 2015 Online Instruction Global Online
Negotiation and Influence Jan 29, 2015 Online Instruction Global Online
Introduction to Drug Safety Jan 29, 2015 ACPE, IACET Online Instruction Global Online
How to Prepare for a Safety Inspection Jan 29, 2015 Online Instruction Global Online
Implementation and Status of Periodic Benefit-Risk Evaluation Reporting (PBRER) in Canada Jan 29, 2015 Online Instruction Global Online
Clinical Statistics for Nonstatisticians Jan 29, 2015 Online Instruction Global Online
Advanced Clinical Statistics for Nonstatisticians Jan 29, 2015 Online Instruction Global Online
Development of a Clinical Study Report Jan 29, 2015 Online Instruction Global Online
Art of Writing a Clinical Overview Jan 29, 2015 Online Instruction Global Online
Introductory Principles and Application of Risk Management within Clinical Operations Jan 29, 2015 Online Instruction Global Online
Seven-Part Series on Pediatric Drug Development - Part 6: Preclinical Toxicology & Safety Jan 29, 2015 Online Instruction Global Online
Complimentary - Need to Reinvent the Clinical Trial? Innovate, Collaborate & Integrate Jan 29, 2015 Online Instruction Global Online
Disruptive Innovation in Medical Information Jan 29, 2015 Online Instruction Global Online
A Tour of FDA Jan 29, 2015 Online Instruction Global Online
A Tour of Health Canada Jan 29, 2015 Online Instruction Global Online
A Tour of Health Europe Jan 29, 2015 Online Instruction Global Online
Aspects of Regulatory History Jan 29, 2015 Online Instruction Global Online
Bioresearch Monitoring Program (BIMO): Introduction Jan 29, 2015 Online Instruction Global Online
The Clinical Development Process: Investigational Product, Plan, and Data Management Jan 29, 2015 Online Instruction Global Online
Ethical Review Boards Jan 29, 2015 Online Instruction Global Online
Ethics as the Foundation to Clinical Research Jan 29, 2015 Online Instruction Global Online
Awareness of FDA Inspections for Pharmaceutical Manufacturers Jan 29, 2015 Online Instruction Global Online
Biotechnology: An Overview of Compliance Considerations Jan 29, 2015 Online Instruction Global Online
Change Control Jan 29, 2015 Online Instruction Global Online
Clinical Trial Audits and Consequences of Non-Compliance Jan 29, 2015 Online Instruction Global Online
Computerized Systems Inspections in the Medical Device Industry Jan 29, 2015 Online Instruction Global Online
European Union Clinical Trials Directive Jan 29, 2015 Online Instruction Global Online
GMP Principals of SOPs Jan 29, 2015 Online Instruction Global Online
GMP Updates - Enforcement Changes at the New FDA Jan 29, 2015 Online Instruction Global Online
GMPs for API Bulk Manufacturers Jan 29, 2015 Online Instruction Global Online
Good Clinical Practices (GCPs) for New Product Investigations Jan 29, 2015 Online Instruction Global Online
Good Laboratory Practices (GLPs) Jan 29, 2015 Online Instruction Global Online
GxPs Jan 29, 2015 Online Instruction Global Online
HIPAA - The Impact on Clinical Research Jan 29, 2015 Online Instruction Global Online
Introduction to GMPs Jan 29, 2015 Online Instruction Global Online
Investigational Product Development Jan 29, 2015 Online Instruction Global Online
ISO 14155: Obligations of Sponsors and Monitors for Medical Device Trials Jan 29, 2015 Online Instruction Global Online
Key Concepts of Process Validation Jan 29, 2015 Online Instruction Global Online
Laboratory Specimens for Clinical Research Jan 29, 2015 Online Instruction Global Online
Medical Device Safety Reporting Jan 29, 2015 Online Instruction Global Online
Orientation to GMP Compliance Jan 29, 2015 Online Instruction Global Online
Overview of the Clinical Research Process Jan 29, 2015 Online Instruction Global Online
Part 11: Electronic Records and Signatures - Application Jan 29, 2015 Online Instruction Global Online
Part 11: Electronic Records; Electronic Signatures Jan 29, 2015 Online Instruction Global Online
Principles of Good Documentation Jan 29, 2015 Online Instruction Global Online
Protection of Human Subjects in Clinical Trials Jan 29, 2015 Online Instruction Global Online
Selecting and Managing Clinical Contract Research Organizations (CROs) Jan 29, 2015 Online Instruction Global Online
Understanding Post-Approval Changes Jan 29, 2015 Online Instruction Global Online
Computerized Systems Inspections in the Pharmaceutical Industry Jan 29, 2015 Online Instruction Global Online
Basics of the PhRMA Code Jan 29, 2015 Online Instruction Global Online
Basics of AdvaMed Code Jan 29, 2015 Online Instruction Global Online
Eucomed Guidelines on Interactions with Healthcare Professionals Jan 29, 2015 Online Instruction Global Online
Introduction to Medical Device Health Care Compliance Jan 29, 2015 Online Instruction Global Online
Foreign Corrupt Practices Act Jan 29, 2015 Online Instruction Global Online
Global Anti-bribery Jan 29, 2015 Online Instruction Global Online
Variations to Marketing Authorisation in Europe Jan 29, 2015 Online Instruction Global Online
Registration of Monoclonal Antibodies Jan 29, 2015 Online Instruction Global Online
How to Gain Approval to Market a Generic Medicinal Product in the USA Jan 29, 2015 Online Instruction Global Online
Pharmacokinetics and Pharmacodynamics in Drug Registration Jan 29, 2015 Online Instruction Global Online
Complimentary Quintiles/DIA Webinar - Giving Your Study The Right Start Toward Success Through Optimal Country and Site Selection Jan 29, 2015 Online Instruction Global Online
Implementing Risk-Based Monitoring: Practical Approaches Jan 29, 2015 Online Instruction Global Online
Complimentary - Innovative Strategies for Developing Safer Cancer Therapies Jan 29, 2015 Online Instruction Global Online
Complimentary - Risk-Based Monitoring: Regulatory Expectation and Operational Application Jan 29, 2015 Online Instruction Global Online
Fundamentals of Project Management for Nonproject Managers Jan 29, 2015 Online Instruction Global Online
Planning and Managing Your Projects Jan 29, 2015 Online Instruction Global Online
Preparing a Clinical Trial Budget Jan 29, 2015 Online Instruction Global Online
Team Building and Development Jan 29, 2015 Online Instruction Global Online
Pricing, Economic, Reimbursement, Market Share (PERMS) Strategy: An Interactive Holistic Approach in Rare Diseases Jan 29, 2015 Online Instruction Global Online
Introduction to the European Union Institutions and Regulatory Authority Jan 29, 2015 Online Instruction Global Online
Introduction to US Institutions and Regulatory Authority (FDA) Jan 29, 2015 Online Instruction Global Online
Introduction to Japanese Institutions and Regulatory Authorities Jan 29, 2015 Online Instruction Global Online
Overview of the CTD and eCTD Jan 29, 2015 Online Instruction Global Online
Introduction to the International Conference on Harmonisation (ICH) Jan 29, 2015 Online Instruction Global Online
The Regulatory Development of a Drug Jan 29, 2015 Online Instruction Global Online
Basics of Clinical Trials Jan 29, 2015 Online Instruction Global Online
How to Register Medicinal Products through the Centralized Procedure Jan 29, 2015 Online Instruction Global Online
How to Register Medicinal Products through the Mutual Recognition Procedure Jan 29, 2015 Online Instruction Global Online
How to Maintain Marketing Approvals in Europe for Centrally Authorised Products Jan 29, 2015 Online Instruction Global Online
How to Register a New Drug in the USA Jan 29, 2015 Online Instruction Global Online
How to Register Medicinal Products through the Decentralized Procedure Jan 29, 2015 Online Instruction Global Online
Access to Unapproved Drugs through Compassionate Use Jan 29, 2015 Online Instruction Global Online
Regulatory Requirements for the Conduct of Clinical Trials in Europe Jan 29, 2015 Online Instruction Global Online
Orphan Drugs in the USA, European Union, and Japan Jan 29, 2015 Online Instruction Global Online
Regulatory Requirements for the Submission of Investigational New Drug Applications in the USA (INDs) Jan 29, 2015 Online Instruction Global Online
Meeting Opportunities with Regulatory Agencies Jan 29, 2015 Online Instruction Global Online
How New Electronic Trial Master File (eTMF) Data Standards Can Enhance Clinical Trial Efficiency and Quality Jan 29, 2015 Online Instruction Global Online
Complimentary - Regulatory Solutions in the Cloud - 10 Questions You Can't Afford NOT to Ask Jan 29, 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 Jan 29, 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 Jan 29, 2015 Online Instruction Global Online
Complimentary - From the Clinic to the CFO: Adaptive Trials and Financial Decision-Making Jan 29, 2015 Online Instruction Global Online
Adverse Event Reporting Requirements: IND and Postmarketing Jan 29, 2015 Online Instruction Global Online
Complimentary - The Affiliate Challenge – How to Improve Compliance and Efficiency when Working with Regional Affiliates Jan 29, 2015 Online Instruction Global Online
The Future of Personalized Medicine and Companion Diagnostics Jan 29, 2015 Online Instruction Global Online
Seven-Part Series on Pediatric Drug Development - Part 1: Overall Challenge: The Vision of Better Medicines for Children Jan 29, 2015 Online Instruction Global Online
Seven-Part Series on Pediatric Drug Development - Part 3: Regulatory Framework EU Jan 29, 2015 Online Instruction Global Online
Seven-Part Pediatric Drug Development Webinar Series - Part 4: Dosing in Children Jan 29, 2015 Online Instruction Global Online
Seven-Part Series on Pediatric Drug Development - Part 2: Regulatory Framework US Overview Jan 29, 2015 Online Instruction Global Online
Seven-Part Series on Pediatric Drug Development - Part 5: Technical Development: Pediatric Formulations Jan 29, 2015 Online Instruction Global Online
Basics of the IND Jan 29, 2015 Online Instruction Global Online
Basics of the NDA Jan 29, 2015 Online Instruction Global Online
Regulatory Aspects of Prescription Drug/Biologics Advertising and Promotional Labeling Jan 29, 2015 Online Instruction Global Online
Seven-Part Series on Pediatric Drug Development - Part 7: Operational Challenges of Pediatric Clinical Trials Jan 29, 2015 Online Instruction Global Online
Supplements and Other Changes to an Approved Application Jan 29, 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 Jan 29, 2015 Online Instruction Global Online
Regulatory Aspects of Prescription Drug/Biologics Advertising and Promotional Labeling Feb 05, 2015 IACET 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 Feb 10, 2015 IACET Online Instruction Global Online
Art of Writing a Clinical Overview Feb 24, 2015 IACET Online Instruction Global Online
Pricing, Economic, Reimbursement, Market Share (PERMS) Strategy: An Interactive Holistic Approach in Rare Diseases Mar 05, 2015 IACET Online Instruction Global Online
Preparing a Clinical Trial Budget Mar 10, 2015 IACET, PMI Online Instruction Global Online
Clinical Data Validation Workshop Mar 25, 2015 Meetings China
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
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