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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 Aug 01, 2014 Online Instruction Global Online
Generic Drug Labeling Proposed Rule and Safety Updates Aug 01, 2014 Online Instruction Global Online
English Literacy and Spanish Transcreation of Patient Documents: Concepts for Low Literacy Materials Aug 01, 2014 Online Instruction Global Online
Emerging Technologies to Rare Disorder Drug Development: Promises and Pitfalls Aug 01, 2014 Online Instruction Global Online
Big Data: Impact of Health Care Reform on Collaborations and Strategies Aug 01, 2014 Online Instruction Global Online
Implementation of the FDASIA Patient Provisions Aug 01, 2014 Online Instruction Global Online
Complimentary: Regulatory and Real World Evidence Challenges of Rare Diseases and Orphan Drugs Aug 01, 2014 Online Instruction Global Online
Variations in the European Union: CMC/Quality Changes Aug 01, 2014 Online Instruction Global Online
Good Pharmacovigilance Practice: How Good has it Proven to be for Industry? Aug 01, 2014 Online Instruction Global Online
Safety and Social Media: Is this the Question or the Answer Aug 01, 2014 Online Instruction Global Online
Pharmacovigilance and Risk Management: Patient Perspective Aug 01, 2014 Online Instruction Global Online
Complimentary Patient-Centeredness and Engagement in Clinical Research: Opportunities for Industry Aug 01, 2014 Online Instruction Global Online
Drug Safety Regulatory Requirements Aug 01, 2014 ACPE, IACET Online Instruction Global Online
Premarketing Clinical Trial Safety Aug 01, 2014 ACPE, IACET Online Instruction Global Online
Postmarketing Safety Management Aug 01, 2014 Online Instruction Global Online
Basics of Signal Detection and Pharmacoepidemiology Aug 01, 2014 Online Instruction Global Online
Safety Audits and Inspections Aug 01, 2014 Online Instruction Global Online
Five-Part Series on Fundamentals of Clinical Pharmacology for Drug Development - Part 1: Fundamentals of Clinical Pharmacology: Pharmacokinetics Aug 01, 2014 Online Instruction Global Online
Pharmacovigilance and Global Harmonization Updates Aug 01, 2014 Online Instruction Global Online
Designed for Success: Utilizing Protocol Quality by Design (QbD) to Plan Clinical Studies Aug 01, 2014 Online Instruction Global Online
Negotiation and Influence Aug 01, 2014 Online Instruction Global Online
China Update: Regulatory Changes and Implications Aug 01, 2014 Online Instruction Global Online
Evaluation and Management of Cardiac Conditions in Oncology Patients Aug 01, 2014 Online Instruction Global Online
Risk Management of Medicinal Products: REMS and RMP - Need for Harmonization Within the ICH Region? Aug 01, 2014 Online Instruction Global Online
Introduction to Drug Safety Aug 01, 2014 ACPE, IACET Online Instruction Global Online
How to Prepare for a Safety Inspection Aug 01, 2014 Online Instruction Global Online
Clinical Statistics for Nonstatisticians Aug 01, 2014 Online Instruction Global Online
Development of a Clinical Study Report Aug 01, 2014 Online Instruction Global Online
Complimentary Biomarker Strategies for More Efficient Early-Phase Drug Development in Alzheimer's Disease Aug 01, 2014 Online Instruction Global Online
CardioVascular Safety: The New Paradigm - Proarrhythmic Assessment of New Drugs without the Thorough QT Study Aug 01, 2014 Online Instruction Global Online
CardioVascular Safety – What are the Key Issues Regarding Blood Pressure Assessment During Clinical Development Aug 01, 2014 Online Instruction Global Online
Introductory Principles and Application of Risk Management within Clinical Operations Aug 01, 2014 Online Instruction Global Online
Electronic Submissions 101 – Essential MS Word and Adobe Acrobat Tools/Skills and Current IT Options Aug 01, 2014 Online Instruction Global Online
A Tour of FDA Aug 01, 2014 Online Instruction Global Online
A Tour of Health Canada Aug 01, 2014 Online Instruction Global Online
A Tour of Health Europe Aug 01, 2014 Online Instruction Global Online
Aspects of Regulatory History Aug 01, 2014 Online Instruction Global Online
Bioresearch Monitoring Program (BIMO): Introduction Aug 01, 2014 Online Instruction Global Online
The Clinical Development Process: Investigational Product, Plan, and Data Management Aug 01, 2014 Online Instruction Global Online
Drug Safety & Adverse Event Reporting Aug 01, 2014 Online Instruction Global Online
Ethical Review Boards Aug 01, 2014 Online Instruction Global Online
Ethics as the Foundation to Clinical Research Aug 01, 2014 Online Instruction Global Online
Awareness of FDA Inspections for Pharmaceutical Manufacturers Aug 01, 2014 Online Instruction Global Online
Biotechnology: An Overview of Compliance Considerations Aug 01, 2014 Online Instruction Global Online
Change Control Aug 01, 2014 Online Instruction Global Online
Clinical Trial Audits and Consequences of Non-Compliance Aug 01, 2014 Online Instruction Global Online
Computerized Systems Inspections in the Medical Device Industry Aug 01, 2014 Online Instruction Global Online
European Union Clinical Trials Directive Aug 01, 2014 Online Instruction Global Online
GMP Principals of SOPs Aug 01, 2014 Online Instruction Global Online
GMP Updates - Enforcement Changes at the New FDA Aug 01, 2014 Online Instruction Global Online
GMPs for API Bulk Manufacturers Aug 01, 2014 Online Instruction Global Online
Good Clinical Practices (GCPs) for New Product Investigations Aug 01, 2014 Online Instruction Global Online
Good Laboratory Practices (GLPs) Aug 01, 2014 Online Instruction Global Online
GxPs Aug 01, 2014 Online Instruction Global Online
HIPAA - The Impact on Clinical Research Aug 01, 2014 Online Instruction Global Online
Introduction to GMPs Aug 01, 2014 Online Instruction Global Online
Investigational Product Development Aug 01, 2014 Online Instruction Global Online
ISO 14155: Obligations of Sponsors and Monitors for Medical Device Trials Aug 01, 2014 Online Instruction Global Online
Key Concepts of Process Validation Aug 01, 2014 Online Instruction Global Online
Laboratory Specimens for Clinical Research Aug 01, 2014 Online Instruction Global Online
Medical Device Safety Reporting Aug 01, 2014 Online Instruction Global Online
Orientation to GMP Compliance Aug 01, 2014 Online Instruction Global Online
Overview of the Clinical Research Process Aug 01, 2014 Online Instruction Global Online
Part 11: Electronic Records and Signatures - Application Aug 01, 2014 Online Instruction Global Online
Part 11: Electronic Records; Electronic Signatures Aug 01, 2014 Online Instruction Global Online
Principles of Good Documentation Aug 01, 2014 Online Instruction Global Online
Protection of Human Subjects in Clinical Trials Aug 01, 2014 Online Instruction Global Online
Selecting and Managing Clinical Contract Research Organizations (CROs) Aug 01, 2014 Online Instruction Global Online
Understanding Post-Approval Changes Aug 01, 2014 Online Instruction Global Online
Computerized Systems Inspections in the Pharmaceutical Industry Aug 01, 2014 Online Instruction Global Online
Basics of the PhRMA Code Aug 01, 2014 Online Instruction Global Online
Basics of AdvaMed Code Aug 01, 2014 Online Instruction Global Online
Eucomed Guidelines on Interactions with Healthcare Professionals Aug 01, 2014 Online Instruction Global Online
Introduction to Medical Device Health Care Compliance Aug 01, 2014 Online Instruction Global Online
Foreign Corrupt Practices Act Aug 01, 2014 Online Instruction Global Online
Global Anti-bribery Aug 01, 2014 Online Instruction Global Online
Variations to Marketing Authorisation in Europe Aug 01, 2014 Online Instruction Global Online
Registration of Monoclonal Antibodies Aug 01, 2014 Online Instruction Global Online
How to Gain Approval to Market a Generic Medicinal Product in the USA Aug 01, 2014 Online Instruction Global Online
Pharmacokinetics and Pharmacodynamics in Drug Registration Aug 01, 2014 Online Instruction Global Online
Measurement in Clinical Trials: An Examination of the FDA Position on Review of Clinical Outcome Assessments (COAs) Aug 01, 2014 Online Instruction Global Online
The Electronic Trial Master File: So Much More than Just a Secure Document Repository Aug 01, 2014 Online Instruction Global Online
Planning and Implementing Large Cardiovascular Outcomes Studies: Opportunities & Challenges Aug 01, 2014 Online Instruction Global Online
Press the Easy Button – Ensure Consistency and Compliance for your Documents through Automation Aug 01, 2014 Online Instruction Global Online
When Outsourcing Stops Making Sense Aug 01, 2014 Online Instruction Global Online
Complimentary Quintiles/DIA Webinar - Giving Your Study The Right Start Toward Success Through Optimal Country and Site Selection Aug 01, 2014 Online Instruction Global Online
Complimentary - Risk-Based Monitoring: Regulatory Expectation and Operational Application Aug 01, 2014 Online Instruction Global Online
Fundamentals of Project Management for Nonproject Managers Aug 01, 2014 Online Instruction Global Online
Planning and Managing Your Project Aug 01, 2014 Online Instruction Global Online
Change Management, Issues Management, Escalation Management Aug 01, 2014 Online Instruction Global Online
Project Risk Management: Dealing with the Certainty of Uncertainty Aug 01, 2014 Online Instruction Global Online
Team Building and Development Aug 01, 2014 Online Instruction Global Online
Preparing a Clinical Trial Budget Aug 01, 2014 Online Instruction Global Online
Introduction to the European Union Institutions and Regulatory Authority Aug 01, 2014 Online Instruction Global Online
Introduction to US Institutions and Regulatory Authority (FDA) Aug 01, 2014 Online Instruction Global Online
Introduction to Japanese Institutions and Regulatory Authorities Aug 01, 2014 Online Instruction Global Online
Overview of the CTD and eCTD Aug 01, 2014 Online Instruction Global Online
Introduction to the International Conference on Harmonisation (ICH) Aug 01, 2014 Online Instruction Global Online
The Regulatory Development of a Drug Aug 01, 2014 Online Instruction Global Online
Basics of Clinical Trials Aug 01, 2014 Online Instruction Global Online
How to Register Medicinal Products through the Centralized Procedure Aug 01, 2014 Online Instruction Global Online
How to Register Medicinal Products through the Mutual Recognition Procedure Aug 01, 2014 Online Instruction Global Online
How to Maintain Marketing Approvals in Europe for Centrally Authorised Products Aug 01, 2014 Online Instruction Global Online
How to Register a New Drug in the USA Aug 01, 2014 Online Instruction Global Online
How to Register Medicinal Products through the Decentralized Procedure Aug 01, 2014 Online Instruction Global Online
Access to Unapproved Drugs through Compassionate Use Aug 01, 2014 Online Instruction Global Online
Regulatory Requirements for the Conduct of Clinical Trials in Europe Aug 01, 2014 Online Instruction Global Online
Orphan Drugs in the USA, European Union, and Japan Aug 01, 2014 Online Instruction Global Online
Regulatory Requirements for the Submission of Investigational New Drug Applications in the USA (INDs) Aug 01, 2014 Online Instruction Global Online
Meeting Opportunities with Regulatory Agencies Aug 01, 2014 Online Instruction Global Online
A Regulatory Perspective of Biosimilars in Emerging Markets Aug 01, 2014 Online Instruction Global Online
Combination Products and Convergence: An Overview of Clinical Benefits, Regulatory Issues & Manufacturing Challenges Aug 01, 2014 Online Instruction Global Online
Strategies for Successfully Introducing REMS to Your Organization: From Development and Implementation and Internal and External Evaluation Aug 01, 2014 Online Instruction Global Online
The Case of the New England Compounding Center: Learning from the Tragedy Aug 01, 2014 Online Instruction Global Online
Complimentary - From the Clinic to the CFO: Adaptive Trials and Financial Decision-Making Aug 01, 2014 Online Instruction Global Online
Complimentary - The Affiliate Challenge – How to Improve Compliance and Efficiency when Working with Regional Affiliates Aug 01, 2014 Online Instruction Global Online
The Future of Personalized Medicine and Companion Diagnostics Aug 01, 2014 Online Instruction Global Online
Seven-Part Series on Pediatric Drug Development - Part 1: Overall Challenge: The Vision of Better Medicines for Children Aug 01, 2014 Online Instruction Global Online
Seven-Part Series on Pediatric Drug Development - Part 3: Regulatory Framework EU Aug 01, 2014 Online Instruction Global Online
Seven-Part Pediatric Drug Development Webinar Series - Part 4: Dosing in Children Aug 01, 2014 Online Instruction Global Online
Seven-Part Series on Pediatric Drug Development - Part 2 Regulatory Framework US Overview Aug 01, 2014 Online Instruction Global Online
Basics of the IND Aug 01, 2014 Online Instruction Global Online
Basics of the NDA Aug 01, 2014 Online Instruction Global Online
Regulatory Aspects of Prescription Drug/Biologics Advertising and Promotional Labeling Aug 01, 2014 Online Instruction Global Online
The Current State of Quality Oversight (QO) in the Pharmaceutical Industry Aug 01, 2014 Online Instruction Global Online
Supplements and Other Changes to an Approved Application Aug 01, 2014 Online Instruction Global Online
Five-Part Series on Fundamentals of Clinical Pharmacology for Drug Development - Part 2: Fundamentals of Clinical Pharmacology: Pharmacodynamics Aug 07, 2014 ACPE, IACET Online Instruction Global Online
Seven-Part Series on Pediatric Drug Development - Part V: Technical Development: Pediatric Formulations Aug 12, 2014 ACPE, IACET Online Instruction Global Online
Team Building and Development Aug 13, 2014 IACET, PMI Online Instruction Global Online
Five-Part Series on Fundamentals of Clinical Pharmacology For Drug Development - Part 3: Principles of Modeling and Simulation Sep 04, 2014 ACPE, IACET 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 Sep 09, 2014 Online Instruction Global Online
Seven-Part Series on Pediatric Drug Development - Part VI: Preclinical Toxicology & Safety Sep 09, 2014 ACPE, IACET Online Instruction Global Online
Art of Writing a Clinical Overview Sep 09, 2014 IACET Online Instruction Global Online
Understanding and Implementing Clinical Data Management in EDC Trials Sep 15, 2014 Meetings China Beijing, China
Strategies for Good Clinical Practice Audits Sep 23, 2014 IACET, RN Online Instruction Global Online
Introduction to Signal Detection and Data Mining Sep 29, 2014 IACET Online Instruction Global Online
Five-Part Series on Fundamentals of Clinical Pharmacology for Drug Development - Part 4: Determining the Safe First Human Dose Oct 09, 2014 ACPE, IACET Online Instruction Global Online
Fact or Fiction: Legal Restrictions to Patient Engagement in Drug Development Oct 14, 2014 Online Instruction Global Online
Seven-Part Series on Pediatric Drug Development - Part VII: Operational Challenges of Pediatric Clinical Trials Oct 14, 2014 ACPE, IACET 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 Oct 21, 2014 Online Instruction Global Online
Negotiation and Influence Oct 30, 2014 IACET, PMI Online Instruction Global Online
Five-Part Series on Fundamentals of Clinical Pharmacology for Drug Development - Part 5: Assessment of QT Prolongation Nov 06, 2014 ACPE, IACET 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 3 - Understanding the Legislation Landscape: Regulatory Updates from the FDA and EMA Nov 12, 2014 Online Instruction Global Online
Review a Global Quality Dossier (CTD) with Concept of Quality by Design (QbD) Dec 08, 2014 In-Person Instruction China