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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.

Find Meetings & Training 

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