Advertisement
DIA
Drug Information Association Logo

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
Clinical Investigator: Module 2 - Conducting The Study Nov 22, 2014 ACPE, CME Online Instruction North America Online
Clinical Investigator: Module 1 - Study Preparation and Initiation Nov 22, 2014 ACPE, CME Online Instruction North America Online
Informed Consent Nov 22, 2014 ACPE Online Instruction North America Online
Crisis Management Nov 22, 2014 ACPE, IACET Online Instruction North America Online
Database Management Nov 22, 2014 ACPE, IACET Online Instruction North America Online
Literature Evaluation Nov 22, 2014 ACPE, IACET Online Instruction North America Online
Literature Searching Nov 22, 2014 ACPE, IACET Online Instruction North America Online
Medical Inquiries Nov 22, 2014 ACPE, IACET Online Instruction North America Online
Medical Writing Nov 22, 2014 IACET Online Instruction North America Online
Product Labeling Nov 22, 2014 ACPE, IACET Online Instruction North America Online
Regulatory Issues Nov 22, 2014 ACPE, IACET Online Instruction North America Online
Statistics for Medical Communications Professionals Nov 22, 2014 ACPE, IACET Online Instruction North America Online
The Use of Mobile Medical Applications as Companions Nov 22, 2014 Online Instruction Global Online
Generic Drug Labeling Proposed Rule and Safety Updates Nov 22, 2014 Online Instruction Global Online
Emerging Technologies to Rare Disorder Drug Development: Promises and Pitfalls Nov 22, 2014 Online Instruction Global Online
Target Product Profile – Strategies to Optimize Drug Development, Product Labeling, and Commercialization Nov 22, 2014 Online Instruction Global Online
The Role of the Clinical Data Manager Nov 22, 2014 Online Instruction Global Online
Implementation of the FDASIA Patient Provisions Nov 22, 2014 Online Instruction Global Online
Complimentary: Regulatory and Real World Evidence Challenges of Rare Diseases and Orphan Drugs Nov 22, 2014 Online Instruction Global Online
Variations in the European Union: CMC/Quality Changes Nov 22, 2014 Online Instruction Global Online
Facets of Drug-Induced Kidney Injury and Regulatory Perspective Nov 22, 2014 Online Instruction Global Online
Impact on Drug Development of Novel Translational Safety Biomarkers for Improved Detection of Drug-Induced Acute Kidney Injury Nov 22, 2014 Online Instruction Global Online
Pharmacovigilance and Risk Management: Patient Perspective Nov 22, 2014 Online Instruction Global Online
Complimentary Patient-Centeredness and Engagement in Clinical Research: Opportunities for Industry Nov 22, 2014 Online Instruction Global Online
Drug Safety Regulatory Requirements Nov 22, 2014 ACPE, IACET Online Instruction Global Online
Premarketing Clinical Trial Safety Nov 22, 2014 ACPE, IACET Online Instruction Global Online
Postmarketing Safety Management Nov 22, 2014 ACPE, IACET Online Instruction Global Online
Basics of Signal Detection and Pharmacoepidemiology Nov 22, 2014 ACPE, IACET Online Instruction Global Online
Safety Audits and Inspections Nov 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 Nov 22, 2014 Online Instruction Global Online
Five-Part Series on Fundamentals of Clinical Pharmacology for Drug Development - Part 2: Fundamentals of Clinical Pharmacology: Pharmacodynamics Nov 22, 2014 Online Instruction Global Online
Pharmacovigilance and Global Harmonization Updates Nov 22, 2014 Online Instruction Global Online
Five-Part Series on Fundamentals of Clinical Pharmacology For Drug Development - Part 3: Principles of Modeling and Simulation Nov 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 Nov 22, 2014 Online Instruction Global Online
Five-Part Series on Fundamentals of Clinical Pharmacology for Drug Development - Part 5: Assessment of QT Prolongation Nov 22, 2014 Online Instruction Global Online
Designed for Success: Utilizing Protocol Quality by Design (QbD) to Plan Clinical Studies Nov 22, 2014 Online Instruction Global Online
Negotiation and Influence Nov 22, 2014 Online Instruction Global Online
China Update: Regulatory Changes and Implications Nov 22, 2014 Online Instruction Global Online
Evaluation and Management of Cardiac Conditions in Oncology Patients Nov 22, 2014 Online Instruction Global Online
Introduction to Drug Safety Nov 22, 2014 ACPE, IACET Online Instruction Global Online
How to Prepare for a Safety Inspection Nov 22, 2014 Online Instruction Global Online
Implementation and Status of Periodic Benefit-Risk Evaluation Reporting (PBRER) in Canada Nov 22, 2014 Online Instruction Global Online
Clinical Statistics for Nonstatisticians Nov 22, 2014 Online Instruction Global Online
Advanced Clinical Statistics for Nonstatisticians Nov 22, 2014 Online Instruction Global Online
Development of a Clinical Study Report Nov 22, 2014 Online Instruction Global Online
Art of Writing a Clinical Overview Nov 22, 2014 Online Instruction Global Online
Introductory Principles and Application of Risk Management within Clinical Operations Nov 22, 2014 Online Instruction Global Online
Seven-Part Series on Pediatric Drug Development - Part 6: Preclinical Toxicology & Safety Nov 22, 2014 Online Instruction Global Online
Electronic Submissions 101 – Essential MS Word and Adobe Acrobat Tools/Skills and Current IT Options Nov 22, 2014 Online Instruction Global Online
Disruptive Innovation in Medical Information Nov 22, 2014 Online Instruction Global Online
A Tour of FDA Nov 22, 2014 Online Instruction Global Online
A Tour of Health Canada Nov 22, 2014 Online Instruction Global Online
A Tour of Health Europe Nov 22, 2014 Online Instruction Global Online
Aspects of Regulatory History Nov 22, 2014 Online Instruction Global Online
Bioresearch Monitoring Program (BIMO): Introduction Nov 22, 2014 Online Instruction Global Online
The Clinical Development Process: Investigational Product, Plan, and Data Management Nov 22, 2014 Online Instruction Global Online
Drug Safety & Adverse Event Reporting Nov 22, 2014 Online Instruction Global Online
Ethical Review Boards Nov 22, 2014 Online Instruction Global Online
Ethics as the Foundation to Clinical Research Nov 22, 2014 Online Instruction Global Online
Awareness of FDA Inspections for Pharmaceutical Manufacturers Nov 22, 2014 Online Instruction Global Online
Biotechnology: An Overview of Compliance Considerations Nov 22, 2014 Online Instruction Global Online
Change Control Nov 22, 2014 Online Instruction Global Online
Clinical Trial Audits and Consequences of Non-Compliance Nov 22, 2014 Online Instruction Global Online
Computerized Systems Inspections in the Medical Device Industry Nov 22, 2014 Online Instruction Global Online
European Union Clinical Trials Directive Nov 22, 2014 Online Instruction Global Online
GMP Principals of SOPs Nov 22, 2014 Online Instruction Global Online
GMP Updates - Enforcement Changes at the New FDA Nov 22, 2014 Online Instruction Global Online
GMPs for API Bulk Manufacturers Nov 22, 2014 Online Instruction Global Online
Good Clinical Practices (GCPs) for New Product Investigations Nov 22, 2014 Online Instruction Global Online
Good Laboratory Practices (GLPs) Nov 22, 2014 Online Instruction Global Online
GxPs Nov 22, 2014 Online Instruction Global Online
HIPAA - The Impact on Clinical Research Nov 22, 2014 Online Instruction Global Online
Introduction to GMPs Nov 22, 2014 Online Instruction Global Online
Investigational Product Development Nov 22, 2014 Online Instruction Global Online
ISO 14155: Obligations of Sponsors and Monitors for Medical Device Trials Nov 22, 2014 Online Instruction Global Online
Key Concepts of Process Validation Nov 22, 2014 Online Instruction Global Online
Laboratory Specimens for Clinical Research Nov 22, 2014 Online Instruction Global Online
Medical Device Safety Reporting Nov 22, 2014 Online Instruction Global Online
Orientation to GMP Compliance Nov 22, 2014 Online Instruction Global Online
Overview of the Clinical Research Process Nov 22, 2014 Online Instruction Global Online
Part 11: Electronic Records and Signatures - Application Nov 22, 2014 Online Instruction Global Online
Part 11: Electronic Records; Electronic Signatures Nov 22, 2014 Online Instruction Global Online
Principles of Good Documentation Nov 22, 2014 Online Instruction Global Online
Protection of Human Subjects in Clinical Trials Nov 22, 2014 Online Instruction Global Online
Selecting and Managing Clinical Contract Research Organizations (CROs) Nov 22, 2014 Online Instruction Global Online
Understanding Post-Approval Changes Nov 22, 2014 Online Instruction Global Online
Computerized Systems Inspections in the Pharmaceutical Industry Nov 22, 2014 Online Instruction Global Online
Basics of the PhRMA Code Nov 22, 2014 Online Instruction Global Online
Basics of AdvaMed Code Nov 22, 2014 Online Instruction Global Online
Eucomed Guidelines on Interactions with Healthcare Professionals Nov 22, 2014 Online Instruction Global Online
Introduction to Medical Device Health Care Compliance Nov 22, 2014 Online Instruction Global Online
Foreign Corrupt Practices Act Nov 22, 2014 Online Instruction Global Online
Global Anti-bribery Nov 22, 2014 Online Instruction Global Online
Variations to Marketing Authorisation in Europe Nov 22, 2014 Online Instruction Global Online
Registration of Monoclonal Antibodies Nov 22, 2014 Online Instruction Global Online
How to Gain Approval to Market a Generic Medicinal Product in the USA Nov 22, 2014 Online Instruction Global Online
Pharmacokinetics and Pharmacodynamics in Drug Registration Nov 22, 2014 Online Instruction Global Online
Complimentary - When Outsourcing Stops Making Sense Nov 22, 2014 Online Instruction Global Online
Complimentary Quintiles/DIA Webinar - Giving Your Study The Right Start Toward Success Through Optimal Country and Site Selection Nov 22, 2014 Online Instruction Global Online
Implementing Risk-Based Monitoring: Practical Approaches Nov 22, 2014 Online Instruction Global Online
Complimentary - Risk-Based Monitoring: Regulatory Expectation and Operational Application Nov 22, 2014 Online Instruction Global Online
Fundamentals of Project Management for Nonproject Managers Nov 22, 2014 Online Instruction Global Online
Planning and Managing Your Projects Nov 22, 2014 Online Instruction Global Online
Preparing a Clinical Trial Budget Nov 22, 2014 Online Instruction Global Online
Team Building and Development Nov 22, 2014 Online Instruction Global Online
Introduction to the European Union Institutions and Regulatory Authority Nov 22, 2014 Online Instruction Global Online
Introduction to US Institutions and Regulatory Authority (FDA) Nov 22, 2014 Online Instruction Global Online
Introduction to Japanese Institutions and Regulatory Authorities Nov 22, 2014 Online Instruction Global Online
Overview of the CTD and eCTD Nov 22, 2014 Online Instruction Global Online
Introduction to the International Conference on Harmonisation (ICH) Nov 22, 2014 Online Instruction Global Online
The Regulatory Development of a Drug Nov 22, 2014 Online Instruction Global Online
Basics of Clinical Trials Nov 22, 2014 Online Instruction Global Online
How to Register Medicinal Products through the Centralized Procedure Nov 22, 2014 Online Instruction Global Online
How to Register Medicinal Products through the Mutual Recognition Procedure Nov 22, 2014 Online Instruction Global Online
How to Maintain Marketing Approvals in Europe for Centrally Authorised Products Nov 22, 2014 Online Instruction Global Online
How to Register a New Drug in the USA Nov 22, 2014 Online Instruction Global Online
How to Register Medicinal Products through the Decentralized Procedure Nov 22, 2014 Online Instruction Global Online
Access to Unapproved Drugs through Compassionate Use Nov 22, 2014 Online Instruction Global Online
Regulatory Requirements for the Conduct of Clinical Trials in Europe Nov 22, 2014 Online Instruction Global Online
Orphan Drugs in the USA, European Union, and Japan Nov 22, 2014 Online Instruction Global Online
Regulatory Requirements for the Submission of Investigational New Drug Applications in the USA (INDs) Nov 22, 2014 Online Instruction Global Online
Meeting Opportunities with Regulatory Agencies Nov 22, 2014 Online Instruction Global Online
Combination Products and Convergence: An Overview of Clinical Benefits, Regulatory Issues & Manufacturing Challenges Nov 22, 2014 Online Instruction Global Online
How New Electronic Trial Master File (eTMF) Data Standards Can Enhance Clinical Trial Efficiency and Quality Nov 22, 2014 Online Instruction Global Online
Complimentary - Regulatory Solutions in the Cloud - 10 Questions You Can't Afford NOT to Ask Nov 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 Nov 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 Nov 22, 2014 Online Instruction Global Online
The Case of the New England Compounding Center: Learning from the Tragedy Nov 22, 2014 Online Instruction Global Online
Complimentary - From the Clinic to the CFO: Adaptive Trials and Financial Decision-Making Nov 22, 2014 Online Instruction Global Online
Adverse Event Reporting Requirements: IND and Postmarketing Nov 22, 2014 Online Instruction Global Online
Complimentary - The Affiliate Challenge – How to Improve Compliance and Efficiency when Working with Regional Affiliates Nov 22, 2014 Online Instruction Global Online
The Future of Personalized Medicine and Companion Diagnostics Nov 22, 2014 Online Instruction Global Online
Seven-Part Series on Pediatric Drug Development - Part 1: Overall Challenge: The Vision of Better Medicines for Children Nov 22, 2014 Online Instruction Global Online
Seven-Part Series on Pediatric Drug Development - Part 3: Regulatory Framework EU Nov 22, 2014 Online Instruction Global Online
Seven-Part Pediatric Drug Development Webinar Series - Part 4: Dosing in Children Nov 22, 2014 Online Instruction Global Online
Seven-Part Series on Pediatric Drug Development - Part 2: Regulatory Framework US Overview Nov 22, 2014 Online Instruction Global Online
Seven-Part Series on Pediatric Drug Development - Part 5: Technical Development: Pediatric Formulations Nov 22, 2014 Online Instruction Global Online
Basics of the IND Nov 22, 2014 Online Instruction Global Online
Basics of the NDA Nov 22, 2014 Online Instruction Global Online
Regulatory Aspects of Prescription Drug/Biologics Advertising and Promotional Labeling Nov 22, 2014 Online Instruction Global Online
Seven-Part Series on Pediatric Drug Development - Part 7: Operational Challenges of Pediatric Clinical Trials Nov 22, 2014 Online Instruction Global Online
Supplements and Other Changes to an Approved Application Nov 22, 2014 Online Instruction Global Online
Clinical Trial Regulations Nov 26, 2014 Online Instruction Global Online
Target Product Profile – Strategies to Optimize Drug Development, Product Labeling, and Commercialization Dec 02, 2014 Online Instruction Global Online
Facets of Drug-Induced Kidney Injury and Regulatory Perspective Dec 03, 2014 ACPE, IACET Online Instruction Global Online
Complimentary - Cardio-Oncology: Innovative Strategies for Mitigating Cardiovascular Risk of New Cancer Therapies Dec 04, 2014 Online Instruction Global Online
Implementing Risk-Based Monitoring: Practical Approaches Dec 09, 2014 ACPE, IACET Online Instruction Global Online
Implementation and Status of Periodic Benefit-Risk Evaluation Reporting (PBRER) in Canada Dec 09, 2014 Online Instruction Global Online
Introduction to Pharmacoepidemiology and Applications in Premarketing and Postmarketing Surveillance, Risk Management and Value Demonstration Jan 25, 2015 In-Person Instruction North America Washington, DC, United States
Pharmacovigilance and Risk Management Planning Jan 25, 2015 In-Person Instruction North America Washington, DC, United States
PBRERs Jan 25, 2015 In-Person Instruction North America Washington, DC, United States
Pharmacovigilance System Master File Jan 25, 2015 In-Person Instruction North America Washington, DC, United States
Pharmacovigilance and Risk Management Strategies 2015 Jan 26, 2015 Meetings North America Washington, DC, United States
Regulatory Aspects of Prescription Drug/Biologics Advertising and Promotional Labeling Feb 05, 2015 IACET Online Instruction Global Online
Joint Adaptive Design and Bayesian Statistics Conference: Drivers of Efficiency in Modern Medical Product Development Feb 11, 2015 Meetings North America Arlington, VA, United States
OPDP/APLB and Compliance 101: A Primer Feb 17, 2015 In-Person Instruction North America Washington, DC, United States
Marketing Pharmaceuticals 2015: Drug/Device Marketing in an Evolving Environment Feb 18, 2015 Meetings North America Washington, DC, United States
Art of Writing a Clinical Overview Feb 24, 2015 IACET Online Instruction Global Online
Introduction to Signal Detection and Data Mining Mar 02, 2015 In-Person Instruction North America Washington, DC, United States
Preparing a Clinical Trial Budget Mar 10, 2015 Online Instruction Global Online
Regulatory Affairs: The IND, NDA, and Postmarketing Mar 15, 2015 In-Person Instruction North America Irvine, CA, United States
Medical & Scientific Communications 2015 Annual Forum Mar 16, 2015 Meetings North America Glendale, AZ, United States
Premarketing Clinical Safety and Pharmacovigilance Mar 23, 2015 In-Person Instruction North America Washington, DC, United States
Preparing for a FDA Advisory Committee Meeting Apr 01, 2015 In-Person Instruction North America Washington, DC, United States
CMC Workshop 2015 Apr 13, 2015 Meetings North America Bethesda, MD, United States
Regulatory Affairs for Biologics Apr 14, 2015 In-Person Instruction North America Bethesda, MD, United States
DIA/FDA Statistics Forum 2015 Apr 20, 2015 Meetings North America North Bethesda, MD, United States
Key Considerations for the Development and Marketing of Biosimilar Products Apr 27, 2015 In-Person Instruction North America Washington, DC, United States
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
eRegulatory and Intelligence Annual Conference May 11, 2015 Meetings North America
Basics of the NDA Phase May 18, 2015 Online Instruction Global Online
How to Prepare for a Safety Inspection Jun 01, 2015 IACET Online Instruction Global Online
DIA 2015 51st Annual Meeting: Develop. Innovate. Advance. Jun 14, 2015 Meetings North America Washington, DC, United States
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
Pragmatic Approaches to Drug Safety Across the Premarketing and Postmarketing Continuum Aug 10, 2015 In-Person Instruction North America
Development of a Clinical Study Report Aug 17, 2015 In-Person Instruction North America
Regulatory Affairs: The IND, NDA, and Postmarketing Aug 17, 2015 In-Person Instruction North America
Clinical Project Management Aug 24, 2015 In-Person Instruction North America Washington, DC, United States
New Drug Product Development and Life Cycle Management Aug 26, 2015 In-Person Instruction North America Washington, DC, United States
Overview of Drug Development in Japan Sep 02, 2015 Online Instruction Global Online
DIA/FDA Oligonucleotide-based Therapeutic Conference 2015 Sep 09, 2015 Meetings North America Washington, DC, United States
Clinical Statistics for Nonstatisticians Sep 28, 2015 ACPE, IACET In-Person Instruction North America Washington, DC, United States
Introduction to Signal Detection and Data Mining Oct 05, 2015 Online Instruction Global Online
Risk Management and Safety Communication Oct 26, 2015 In-Person Instruction North America Washington, DC, United States
Postmarketing Drug Safety & Pharmacovigilance Nov 09, 2015 In-Person Instruction North America
Regulatory Affairs: The IND, NDA, and Postmarketing Nov 09, 2015 In-Person Instruction North America
Navigating Chemistry, Manufacturing and Controls Through the Drug Development Process Nov 09, 2015 In-Person Instruction North America
Advanced Clinical Statistics for NonStatisticians Nov 11, 2015 ACPE, IACET In-Person Instruction North America