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 Dec 23, 2014 ACPE, CME Online Instruction North America Online
Clinical Investigator: Module 1 - Study Preparation and Initiation Dec 23, 2014 ACPE, CME Online Instruction North America Online
Informed Consent Dec 23, 2014 ACPE Online Instruction North America Online
Crisis Management Dec 23, 2014 ACPE, IACET Online Instruction North America Online
Database Management Dec 23, 2014 ACPE, IACET Online Instruction North America Online
Literature Evaluation Dec 23, 2014 ACPE, IACET Online Instruction North America Online
Literature Searching Dec 23, 2014 ACPE, IACET Online Instruction North America Online
Medical Inquiries Dec 23, 2014 ACPE, IACET Online Instruction North America Online
Medical Writing Dec 23, 2014 IACET Online Instruction North America Online
Product Labeling Dec 23, 2014 ACPE, IACET Online Instruction North America Online
Regulatory Issues Dec 23, 2014 ACPE, IACET Online Instruction North America Online
Statistics for Medical Communications Professionals Dec 23, 2014 ACPE, IACET Online Instruction North America Online
The Use of Mobile Medical Applications as Companions Dec 23, 2014 Online Instruction Global Online
Generic Drug Labeling Proposed Rule and Safety Updates Dec 23, 2014 Online Instruction Global Online
Emerging Technologies to Rare Disorder Drug Development: Promises and Pitfalls Dec 23, 2014 Online Instruction Global Online
Target Product Profile – Strategies to Optimize Drug Development, Product Labeling, and Commercialization Dec 23, 2014 Online Instruction Global Online
The Role of the Clinical Data Manager Dec 23, 2014 Online Instruction Global Online
Implementation of the FDASIA Patient Provisions Dec 23, 2014 Online Instruction Global Online
Complimentary: Regulatory and Real World Evidence Challenges of Rare Diseases and Orphan Drugs Dec 23, 2014 Online Instruction Global Online
Variations in the European Union: CMC/Quality Changes Dec 23, 2014 Online Instruction Global Online
Proarrhythmia Dec 23, 2014 Online Instruction Global Online
Facets of Drug-Induced Kidney Injury and Regulatory Perspective Dec 23, 2014 Online Instruction Global Online
Impact on Drug Development of Novel Translational Safety Biomarkers for Improved Detection of Drug-Induced Acute Kidney Injury Dec 23, 2014 Online Instruction Global Online
Pharmacovigilance and Risk Management: Patient Perspective Dec 23, 2014 Online Instruction Global Online
Complimentary Patient-Centeredness and Engagement in Clinical Research: Opportunities for Industry Dec 23, 2014 Online Instruction Global Online
Drug Safety Regulatory Requirements Dec 23, 2014 ACPE, IACET Online Instruction Global Online
Premarketing Clinical Trial Safety Dec 23, 2014 ACPE, IACET Online Instruction Global Online
Postmarketing Safety Management Dec 23, 2014 ACPE, IACET Online Instruction Global Online
Basics of Signal Detection and Pharmacoepidemiology Dec 23, 2014 ACPE, IACET Online Instruction Global Online
Safety Audits and Inspections Dec 23, 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 23, 2014 Online Instruction Global Online
Five-Part Series on Fundamentals of Clinical Pharmacology for Drug Development - Part 2: Fundamentals of Clinical Pharmacology: Pharmacodynamics Dec 23, 2014 Online Instruction Global Online
Pharmacovigilance and Global Harmonization Updates Dec 23, 2014 Online Instruction Global Online
Five-Part Series on Fundamentals of Clinical Pharmacology For Drug Development - Part 3: Principles of Modeling and Simulation Dec 23, 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 23, 2014 Online Instruction Global Online
Five-Part Series on Fundamentals of Clinical Pharmacology for Drug Development - Part 5: Assessment of QT Prolongation Dec 23, 2014 Online Instruction Global Online
Designed for Success: Utilizing Protocol Quality by Design (QbD) to Plan Clinical Studies Dec 23, 2014 Online Instruction Global Online
Negotiation and Influence Dec 23, 2014 Online Instruction Global Online
Introduction to Drug Safety Dec 23, 2014 ACPE, IACET Online Instruction Global Online
How to Prepare for a Safety Inspection Dec 23, 2014 Online Instruction Global Online
Implementation and Status of Periodic Benefit-Risk Evaluation Reporting (PBRER) in Canada Dec 23, 2014 Online Instruction Global Online
Clinical Statistics for Nonstatisticians Dec 23, 2014 Online Instruction Global Online
Advanced Clinical Statistics for Nonstatisticians Dec 23, 2014 Online Instruction Global Online
Development of a Clinical Study Report Dec 23, 2014 Online Instruction Global Online
Art of Writing a Clinical Overview Dec 23, 2014 Online Instruction Global Online
Introductory Principles and Application of Risk Management within Clinical Operations Dec 23, 2014 Online Instruction Global Online
Seven-Part Series on Pediatric Drug Development - Part 6: Preclinical Toxicology & Safety Dec 23, 2014 Online Instruction Global Online
Complimentary - Need to Reinvent the Clinical Trial? Innovate, Collaborate & Integrate Dec 23, 2014 Online Instruction Global Online
Disruptive Innovation in Medical Information Dec 23, 2014 Online Instruction Global Online
A Tour of FDA Dec 23, 2014 Online Instruction Global Online
A Tour of Health Canada Dec 23, 2014 Online Instruction Global Online
A Tour of Health Europe Dec 23, 2014 Online Instruction Global Online
Aspects of Regulatory History Dec 23, 2014 Online Instruction Global Online
Bioresearch Monitoring Program (BIMO): Introduction Dec 23, 2014 Online Instruction Global Online
The Clinical Development Process: Investigational Product, Plan, and Data Management Dec 23, 2014 Online Instruction Global Online
Drug Safety & Adverse Event Reporting Dec 23, 2014 Online Instruction Global Online
Ethical Review Boards Dec 23, 2014 Online Instruction Global Online
Ethics as the Foundation to Clinical Research Dec 23, 2014 Online Instruction Global Online
Awareness of FDA Inspections for Pharmaceutical Manufacturers Dec 23, 2014 Online Instruction Global Online
Biotechnology: An Overview of Compliance Considerations Dec 23, 2014 Online Instruction Global Online
Change Control Dec 23, 2014 Online Instruction Global Online
Clinical Trial Audits and Consequences of Non-Compliance Dec 23, 2014 Online Instruction Global Online
Computerized Systems Inspections in the Medical Device Industry Dec 23, 2014 Online Instruction Global Online
European Union Clinical Trials Directive Dec 23, 2014 Online Instruction Global Online
GMP Principals of SOPs Dec 23, 2014 Online Instruction Global Online
GMP Updates - Enforcement Changes at the New FDA Dec 23, 2014 Online Instruction Global Online
GMPs for API Bulk Manufacturers Dec 23, 2014 Online Instruction Global Online
Good Clinical Practices (GCPs) for New Product Investigations Dec 23, 2014 Online Instruction Global Online
Good Laboratory Practices (GLPs) Dec 23, 2014 Online Instruction Global Online
GxPs Dec 23, 2014 Online Instruction Global Online
HIPAA - The Impact on Clinical Research Dec 23, 2014 Online Instruction Global Online
Introduction to GMPs Dec 23, 2014 Online Instruction Global Online
Investigational Product Development Dec 23, 2014 Online Instruction Global Online
ISO 14155: Obligations of Sponsors and Monitors for Medical Device Trials Dec 23, 2014 Online Instruction Global Online
Key Concepts of Process Validation Dec 23, 2014 Online Instruction Global Online
Laboratory Specimens for Clinical Research Dec 23, 2014 Online Instruction Global Online
Medical Device Safety Reporting Dec 23, 2014 Online Instruction Global Online
Orientation to GMP Compliance Dec 23, 2014 Online Instruction Global Online
Overview of the Clinical Research Process Dec 23, 2014 Online Instruction Global Online
Part 11: Electronic Records and Signatures - Application Dec 23, 2014 Online Instruction Global Online
Part 11: Electronic Records; Electronic Signatures Dec 23, 2014 Online Instruction Global Online
Principles of Good Documentation Dec 23, 2014 Online Instruction Global Online
Protection of Human Subjects in Clinical Trials Dec 23, 2014 Online Instruction Global Online
Selecting and Managing Clinical Contract Research Organizations (CROs) Dec 23, 2014 Online Instruction Global Online
Understanding Post-Approval Changes Dec 23, 2014 Online Instruction Global Online
Computerized Systems Inspections in the Pharmaceutical Industry Dec 23, 2014 Online Instruction Global Online
Basics of the PhRMA Code Dec 23, 2014 Online Instruction Global Online
Basics of AdvaMed Code Dec 23, 2014 Online Instruction Global Online
Eucomed Guidelines on Interactions with Healthcare Professionals Dec 23, 2014 Online Instruction Global Online
Introduction to Medical Device Health Care Compliance Dec 23, 2014 Online Instruction Global Online
Foreign Corrupt Practices Act Dec 23, 2014 Online Instruction Global Online
Global Anti-bribery Dec 23, 2014 Online Instruction Global Online
Variations to Marketing Authorisation in Europe Dec 23, 2014 Online Instruction Global Online
Registration of Monoclonal Antibodies Dec 23, 2014 Online Instruction Global Online
How to Gain Approval to Market a Generic Medicinal Product in the USA Dec 23, 2014 Online Instruction Global Online
Pharmacokinetics and Pharmacodynamics in Drug Registration Dec 23, 2014 Online Instruction Global Online
Complimentary Quintiles/DIA Webinar - Giving Your Study The Right Start Toward Success Through Optimal Country and Site Selection Dec 23, 2014 Online Instruction Global Online
Implementing Risk-Based Monitoring: Practical Approaches Dec 23, 2014 Online Instruction Global Online
Complimentary - Innovative Strategies for Developing Safer Cancer Therapies Dec 23, 2014 Online Instruction Global Online
Complimentary - Risk-Based Monitoring: Regulatory Expectation and Operational Application Dec 23, 2014 Online Instruction Global Online
Fundamentals of Project Management for Nonproject Managers Dec 23, 2014 Online Instruction Global Online
Planning and Managing Your Projects Dec 23, 2014 Online Instruction Global Online
Preparing a Clinical Trial Budget Dec 23, 2014 Online Instruction Global Online
Team Building and Development Dec 23, 2014 Online Instruction Global Online
Introduction to the European Union Institutions and Regulatory Authority Dec 23, 2014 Online Instruction Global Online
Introduction to US Institutions and Regulatory Authority (FDA) Dec 23, 2014 Online Instruction Global Online
Introduction to Japanese Institutions and Regulatory Authorities Dec 23, 2014 Online Instruction Global Online
Overview of the CTD and eCTD Dec 23, 2014 Online Instruction Global Online
Introduction to the International Conference on Harmonisation (ICH) Dec 23, 2014 Online Instruction Global Online
The Regulatory Development of a Drug Dec 23, 2014 Online Instruction Global Online
Basics of Clinical Trials Dec 23, 2014 Online Instruction Global Online
How to Register Medicinal Products through the Centralized Procedure Dec 23, 2014 Online Instruction Global Online
How to Register Medicinal Products through the Mutual Recognition Procedure Dec 23, 2014 Online Instruction Global Online
How to Maintain Marketing Approvals in Europe for Centrally Authorised Products Dec 23, 2014 Online Instruction Global Online
How to Register a New Drug in the USA Dec 23, 2014 Online Instruction Global Online
How to Register Medicinal Products through the Decentralized Procedure Dec 23, 2014 Online Instruction Global Online
Access to Unapproved Drugs through Compassionate Use Dec 23, 2014 Online Instruction Global Online
Regulatory Requirements for the Conduct of Clinical Trials in Europe Dec 23, 2014 Online Instruction Global Online
Orphan Drugs in the USA, European Union, and Japan Dec 23, 2014 Online Instruction Global Online
Regulatory Requirements for the Submission of Investigational New Drug Applications in the USA (INDs) Dec 23, 2014 Online Instruction Global Online
Meeting Opportunities with Regulatory Agencies Dec 23, 2014 Online Instruction Global Online
How New Electronic Trial Master File (eTMF) Data Standards Can Enhance Clinical Trial Efficiency and Quality Dec 23, 2014 Online Instruction Global Online
Complimentary - Regulatory Solutions in the Cloud - 10 Questions You Can't Afford NOT to Ask Dec 23, 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 23, 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 23, 2014 Online Instruction Global Online
Complimentary - From the Clinic to the CFO: Adaptive Trials and Financial Decision-Making Dec 23, 2014 Online Instruction Global Online
Adverse Event Reporting Requirements: IND and Postmarketing Dec 23, 2014 Online Instruction Global Online
Complimentary - The Affiliate Challenge – How to Improve Compliance and Efficiency when Working with Regional Affiliates Dec 23, 2014 Online Instruction Global Online
The Future of Personalized Medicine and Companion Diagnostics Dec 23, 2014 Online Instruction Global Online
Seven-Part Series on Pediatric Drug Development - Part 1: Overall Challenge: The Vision of Better Medicines for Children Dec 23, 2014 Online Instruction Global Online
Seven-Part Series on Pediatric Drug Development - Part 3: Regulatory Framework EU Dec 23, 2014 Online Instruction Global Online
Seven-Part Pediatric Drug Development Webinar Series - Part 4: Dosing in Children Dec 23, 2014 Online Instruction Global Online
Seven-Part Series on Pediatric Drug Development - Part 2: Regulatory Framework US Overview Dec 23, 2014 Online Instruction Global Online
Seven-Part Series on Pediatric Drug Development - Part 5: Technical Development: Pediatric Formulations Dec 23, 2014 Online Instruction Global Online
Basics of the IND Dec 23, 2014 Online Instruction Global Online
Basics of the NDA Dec 23, 2014 Online Instruction Global Online
Regulatory Aspects of Prescription Drug/Biologics Advertising and Promotional Labeling Dec 23, 2014 Online Instruction Global Online
Seven-Part Series on Pediatric Drug Development - Part 7: Operational Challenges of Pediatric Clinical Trials Dec 23, 2014 Online Instruction Global Online
Supplements and Other Changes to an Approved Application Dec 23, 2014 Online Instruction Global Online
Introduction to Pharmacoepidemiology and Applications in Premarketing and Postmarketing Surveillance, Risk Management and Value Demonstration Jan 25, 2015 IACET, RN In-Person Instruction North America Washington, DC, United States
Pharmacovigilance and Risk Management Planning Jan 25, 2015 ACPE, IACET, RN In-Person Instruction North America Washington, DC, United States
PBRERs Jan 25, 2015 IACET, RN In-Person Instruction North America Washington, DC, United States
Pharmacovigilance System Master File Jan 25, 2015 IACET, RN In-Person Instruction North America Washington, DC, United States
Pharmacovigilance and Risk Management Strategies 2015 Jan 26, 2015 ACPE, CME, IACET, RN 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
Bayesian Methods for Drug Safety Evaluation and Signal Detection Feb 10, 2015 In-Person Instruction North America Arlington, VA, United States
Use of Historical Data in Clinical Trials Feb 10, 2015 In-Person Instruction North America Arlington, VA, United States
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 Mar 30, 2015 IACET 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 2015 Forum 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 Philadelphia, PA, United States
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 10, 2015 IACET In-Person Instruction North America
Regulatory Affairs: The IND, NDA, and Postmarketing Aug 10, 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 Philadelphia, PA, United States
Regulatory Affairs: The IND, NDA, and Postmarketing Nov 09, 2015 In-Person Instruction North America Philadelphia, PA, United States
Navigating Chemistry, Manufacturing and Controls Through the Drug Development Process Nov 09, 2015 In-Person Instruction North America Philadelphia, PA, United States
Advanced Clinical Statistics for NonStatisticians Nov 11, 2015 ACPE, IACET In-Person Instruction North America Philadelphia, PA, United States