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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
Pragmatic Approaches to Drug Safety Across the Premarketing and Postmarketing Continuum Aug 18, 2014 ACPE, IACET In-Person Instruction North America Boston, MA, United States
Regulatory Affairs: The IND, NDA, and Postmarketing Aug 18, 2014 IACET In-Person Instruction North America Boston, MA, United States
Project Risk Management Aug 20, 2014 IACET, PMI In-Person Instruction North America Boston, MA, United States
Clinical Investigator: Module 2 - Conducting The Study Aug 21, 2014 ACPE, CME Online Instruction North America Online
Clinical Investigator: Module 1 - Study Preparation and Initiation Aug 21, 2014 ACPE, CME Online Instruction North America Online
Informed Consent Aug 21, 2014 ACPE Online Instruction North America Online
Crisis Management Aug 21, 2014 ACPE, IACET Online Instruction North America Online
Database Management Aug 21, 2014 ACPE, IACET Online Instruction North America Online
Literature Evaluation Aug 21, 2014 ACPE, IACET Online Instruction North America Online
Literature Searching Aug 21, 2014 ACPE, IACET Online Instruction North America Online
Medical Inquiries Aug 21, 2014 ACPE, IACET Online Instruction North America Online
Medical Writing Aug 21, 2014 IACET Online Instruction North America Online
Product Labeling Aug 21, 2014 ACPE, IACET Online Instruction North America Online
Regulatory Issues Aug 21, 2014 ACPE, IACET Online Instruction North America Online
Statistics for Medical Communications Professionals Aug 21, 2014 ACPE, IACET Online Instruction North America Online
The Use of Mobile Medical Applications as Companions Aug 21, 2014 Online Instruction Global Online
Generic Drug Labeling Proposed Rule and Safety Updates Aug 21, 2014 Online Instruction Global Online
English Literacy and Spanish Transcreation of Patient Documents: Concepts for Low Literacy Materials Aug 21, 2014 Online Instruction Global Online
Emerging Technologies to Rare Disorder Drug Development: Promises and Pitfalls Aug 21, 2014 Online Instruction Global Online
Big Data: Impact of Health Care Reform on Collaborations and Strategies Aug 21, 2014 Online Instruction Global Online
Implementation of the FDASIA Patient Provisions Aug 21, 2014 Online Instruction Global Online
Complimentary: Regulatory and Real World Evidence Challenges of Rare Diseases and Orphan Drugs Aug 21, 2014 Online Instruction Global Online
Variations in the European Union: CMC/Quality Changes Aug 21, 2014 Online Instruction Global Online
Good Pharmacovigilance Practice: How Good has it Proven to be for Industry? Aug 21, 2014 Online Instruction Global Online
Safety and Social Media: Is this the Question or the Answer Aug 21, 2014 Online Instruction Global Online
Pharmacovigilance and Risk Management: Patient Perspective Aug 21, 2014 Online Instruction Global Online
Complimentary Patient-Centeredness and Engagement in Clinical Research: Opportunities for Industry Aug 21, 2014 Online Instruction Global Online
Drug Safety Regulatory Requirements Aug 21, 2014 ACPE, IACET Online Instruction Global Online
Premarketing Clinical Trial Safety Aug 21, 2014 ACPE, IACET Online Instruction Global Online
Postmarketing Safety Management Aug 21, 2014 Online Instruction Global Online
Basics of Signal Detection and Pharmacoepidemiology Aug 21, 2014 ACPE, IACET Online Instruction Global Online
Safety Audits and Inspections Aug 21, 2014 Online Instruction Global Online
Five-Part Series on Fundamentals of Clinical Pharmacology for Drug Development - Part 1: Fundamentals of Clinical Pharmacology: Pharmacokinetics Aug 21, 2014 Online Instruction Global Online
Five-Part Series on Fundamentals of Clinical Pharmacology for Drug Development - Part 2: Fundamentals of Clinical Pharmacology: Pharmacodynamics Aug 21, 2014 Online Instruction Global Online
Pharmacovigilance and Global Harmonization Updates Aug 21, 2014 Online Instruction Global Online
Designed for Success: Utilizing Protocol Quality by Design (QbD) to Plan Clinical Studies Aug 21, 2014 Online Instruction Global Online
Negotiation and Influence Aug 21, 2014 Online Instruction Global Online
China Update: Regulatory Changes and Implications Aug 21, 2014 Online Instruction Global Online
Evaluation and Management of Cardiac Conditions in Oncology Patients Aug 21, 2014 Online Instruction Global Online
Risk Management of Medicinal Products: REMS and RMP - Need for Harmonization Within the ICH Region? Aug 21, 2014 Online Instruction Global Online
Introduction to Drug Safety Aug 21, 2014 ACPE, IACET Online Instruction Global Online
How to Prepare for a Safety Inspection Aug 21, 2014 Online Instruction Global Online
Clinical Statistics for Nonstatisticians Aug 21, 2014 Online Instruction Global Online
Advanced Clinical Statistics for Nonstatisticians Aug 21, 2014 Online Instruction Global Online
Development of a Clinical Study Report Aug 21, 2014 Online Instruction Global Online
CardioVascular Safety: The New Paradigm - Proarrhythmic Assessment of New Drugs without the Thorough QT Study Aug 21, 2014 Online Instruction Global Online
CardioVascular Safety – What are the Key Issues Regarding Blood Pressure Assessment During Clinical Development Aug 21, 2014 Online Instruction Global Online
Introductory Principles and Application of Risk Management within Clinical Operations Aug 21, 2014 Online Instruction Global Online
Electronic Submissions 101 – Essential MS Word and Adobe Acrobat Tools/Skills and Current IT Options Aug 21, 2014 Online Instruction Global Online
A Tour of FDA Aug 21, 2014 Online Instruction Global Online
A Tour of Health Canada Aug 21, 2014 Online Instruction Global Online
A Tour of Health Europe Aug 21, 2014 Online Instruction Global Online
Aspects of Regulatory History Aug 21, 2014 Online Instruction Global Online
Bioresearch Monitoring Program (BIMO): Introduction Aug 21, 2014 Online Instruction Global Online
The Clinical Development Process: Investigational Product, Plan, and Data Management Aug 21, 2014 Online Instruction Global Online
Drug Safety & Adverse Event Reporting Aug 21, 2014 Online Instruction Global Online
Ethical Review Boards Aug 21, 2014 Online Instruction Global Online
Ethics as the Foundation to Clinical Research Aug 21, 2014 Online Instruction Global Online
Awareness of FDA Inspections for Pharmaceutical Manufacturers Aug 21, 2014 Online Instruction Global Online
Biotechnology: An Overview of Compliance Considerations Aug 21, 2014 Online Instruction Global Online
Change Control Aug 21, 2014 Online Instruction Global Online
Clinical Trial Audits and Consequences of Non-Compliance Aug 21, 2014 Online Instruction Global Online
Computerized Systems Inspections in the Medical Device Industry Aug 21, 2014 Online Instruction Global Online
European Union Clinical Trials Directive Aug 21, 2014 Online Instruction Global Online
GMP Principals of SOPs Aug 21, 2014 Online Instruction Global Online
GMP Updates - Enforcement Changes at the New FDA Aug 21, 2014 Online Instruction Global Online
GMPs for API Bulk Manufacturers Aug 21, 2014 Online Instruction Global Online
Good Clinical Practices (GCPs) for New Product Investigations Aug 21, 2014 Online Instruction Global Online
Good Laboratory Practices (GLPs) Aug 21, 2014 Online Instruction Global Online
GxPs Aug 21, 2014 Online Instruction Global Online
HIPAA - The Impact on Clinical Research Aug 21, 2014 Online Instruction Global Online
Introduction to GMPs Aug 21, 2014 Online Instruction Global Online
Investigational Product Development Aug 21, 2014 Online Instruction Global Online
ISO 14155: Obligations of Sponsors and Monitors for Medical Device Trials Aug 21, 2014 Online Instruction Global Online
Key Concepts of Process Validation Aug 21, 2014 Online Instruction Global Online
Laboratory Specimens for Clinical Research Aug 21, 2014 Online Instruction Global Online
Medical Device Safety Reporting Aug 21, 2014 Online Instruction Global Online
Orientation to GMP Compliance Aug 21, 2014 Online Instruction Global Online
Overview of the Clinical Research Process Aug 21, 2014 Online Instruction Global Online
Part 11: Electronic Records and Signatures - Application Aug 21, 2014 Online Instruction Global Online
Part 11: Electronic Records; Electronic Signatures Aug 21, 2014 Online Instruction Global Online
Principles of Good Documentation Aug 21, 2014 Online Instruction Global Online
Protection of Human Subjects in Clinical Trials Aug 21, 2014 Online Instruction Global Online
Selecting and Managing Clinical Contract Research Organizations (CROs) Aug 21, 2014 Online Instruction Global Online
Understanding Post-Approval Changes Aug 21, 2014 Online Instruction Global Online
Computerized Systems Inspections in the Pharmaceutical Industry Aug 21, 2014 Online Instruction Global Online
Basics of the PhRMA Code Aug 21, 2014 Online Instruction Global Online
Basics of AdvaMed Code Aug 21, 2014 Online Instruction Global Online
Eucomed Guidelines on Interactions with Healthcare Professionals Aug 21, 2014 Online Instruction Global Online
Introduction to Medical Device Health Care Compliance Aug 21, 2014 Online Instruction Global Online
Foreign Corrupt Practices Act Aug 21, 2014 Online Instruction Global Online
Global Anti-bribery Aug 21, 2014 Online Instruction Global Online
Variations to Marketing Authorisation in Europe Aug 21, 2014 Online Instruction Global Online
Registration of Monoclonal Antibodies Aug 21, 2014 Online Instruction Global Online
How to Gain Approval to Market a Generic Medicinal Product in the USA Aug 21, 2014 Online Instruction Global Online
Pharmacokinetics and Pharmacodynamics in Drug Registration Aug 21, 2014 Online Instruction Global Online
Measurement in Clinical Trials: An Examination of the FDA Position on Review of Clinical Outcome Assessments (COAs) Aug 21, 2014 Online Instruction Global Online
The Electronic Trial Master File: So Much More than Just a Secure Document Repository Aug 21, 2014 Online Instruction Global Online
Planning and Implementing Large Cardiovascular Outcomes Studies: Opportunities & Challenges Aug 21, 2014 Online Instruction Global Online
Press the Easy Button – Ensure Consistency and Compliance for your Documents through Automation Aug 21, 2014 Online Instruction Global Online
When Outsourcing Stops Making Sense Aug 21, 2014 Online Instruction Global Online
Complimentary Quintiles/DIA Webinar - Giving Your Study The Right Start Toward Success Through Optimal Country and Site Selection Aug 21, 2014 Online Instruction Global Online
Complimentary - Risk-Based Monitoring: Regulatory Expectation and Operational Application Aug 21, 2014 Online Instruction Global Online
Fundamentals of Project Management for Nonproject Managers Aug 21, 2014 Online Instruction Global Online
Planning and Managing Your Project Aug 21, 2014 Online Instruction Global Online
Planning and Managing Your Projects Aug 21, 2014 Online Instruction Global Online
Change Management, Issues Management, Escalation Management Aug 21, 2014 Online Instruction Global Online
Project Risk Management: Dealing with the Certainty of Uncertainty Aug 21, 2014 Online Instruction Global Online
Team Building and Development Aug 21, 2014 Online Instruction Global Online
Preparing a Clinical Trial Budget Aug 21, 2014 Online Instruction Global Online
Team Building and Development Aug 21, 2014 Online Instruction Global Online
Introduction to the European Union Institutions and Regulatory Authority Aug 21, 2014 Online Instruction Global Online
Introduction to US Institutions and Regulatory Authority (FDA) Aug 21, 2014 Online Instruction Global Online
Introduction to Japanese Institutions and Regulatory Authorities Aug 21, 2014 Online Instruction Global Online
Overview of the CTD and eCTD Aug 21, 2014 Online Instruction Global Online
Introduction to the International Conference on Harmonisation (ICH) Aug 21, 2014 Online Instruction Global Online
The Regulatory Development of a Drug Aug 21, 2014 Online Instruction Global Online
Basics of Clinical Trials Aug 21, 2014 Online Instruction Global Online
How to Register Medicinal Products through the Centralized Procedure Aug 21, 2014 Online Instruction Global Online
How to Register Medicinal Products through the Mutual Recognition Procedure Aug 21, 2014 Online Instruction Global Online
How to Maintain Marketing Approvals in Europe for Centrally Authorised Products Aug 21, 2014 Online Instruction Global Online
How to Register a New Drug in the USA Aug 21, 2014 Online Instruction Global Online
How to Register Medicinal Products through the Decentralized Procedure Aug 21, 2014 Online Instruction Global Online
Access to Unapproved Drugs through Compassionate Use Aug 21, 2014 Online Instruction Global Online
Regulatory Requirements for the Conduct of Clinical Trials in Europe Aug 21, 2014 Online Instruction Global Online
Orphan Drugs in the USA, European Union, and Japan Aug 21, 2014 Online Instruction Global Online
Regulatory Requirements for the Submission of Investigational New Drug Applications in the USA (INDs) Aug 21, 2014 Online Instruction Global Online
Meeting Opportunities with Regulatory Agencies Aug 21, 2014 Online Instruction Global Online
A Regulatory Perspective of Biosimilars in Emerging Markets Aug 21, 2014 Online Instruction Global Online
Combination Products and Convergence: An Overview of Clinical Benefits, Regulatory Issues & Manufacturing Challenges Aug 21, 2014 Online Instruction Global Online
Strategies for Successfully Introducing REMS to Your Organization: From Development and Implementation and Internal and External Evaluation Aug 21, 2014 Online Instruction Global Online
The Case of the New England Compounding Center: Learning from the Tragedy Aug 21, 2014 Online Instruction Global Online
Complimentary - From the Clinic to the CFO: Adaptive Trials and Financial Decision-Making Aug 21, 2014 Online Instruction Global Online
Adverse Event Reporting Requirements: IND and Postmarketing Aug 21, 2014 Online Instruction Global Online
Complimentary - The Affiliate Challenge – How to Improve Compliance and Efficiency when Working with Regional Affiliates Aug 21, 2014 Online Instruction Global Online
The Future of Personalized Medicine and Companion Diagnostics Aug 21, 2014 Online Instruction Global Online
Seven-Part Series on Pediatric Drug Development - Part 1: Overall Challenge: The Vision of Better Medicines for Children Aug 21, 2014 Online Instruction Global Online
Seven-Part Series on Pediatric Drug Development - Part 3: Regulatory Framework EU Aug 21, 2014 Online Instruction Global Online
Seven-Part Pediatric Drug Development Webinar Series - Part 4: Dosing in Children Aug 21, 2014 Online Instruction Global Online
Seven-Part Series on Pediatric Drug Development - Part 2 Regulatory Framework US Overview Aug 21, 2014 Online Instruction Global Online
Seven-Part Series on Pediatric Drug Development - Part V: Technical Development: Pediatric Formulations Aug 21, 2014 Online Instruction Global Online
Basics of the IND Aug 21, 2014 Online Instruction Global Online
Basics of the NDA Aug 21, 2014 Online Instruction Global Online
Regulatory Aspects of Prescription Drug/Biologics Advertising and Promotional Labeling Aug 21, 2014 Online Instruction Global Online
The Current State of Quality Oversight (QO) in the Pharmaceutical Industry Aug 21, 2014 Online Instruction Global Online
Supplements and Other Changes to an Approved Application Aug 21, 2014 Online Instruction Global Online
Drug Induced Liver Injury (DILI) Sep 04, 2014 In-Person Instruction China Shanghai, China
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
Overview of Drug Development Sep 08, 2014 IACET, PMI In-Person Instruction North America Horsham, PA, United States
Key Considerations for the Development and Marketing of Biosimilar Products Sep 09, 2014 IACET In-Person Instruction North America Horsham, PA, United States
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 IACET 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
Development of a Clinical Study Report Sep 15, 2014 IACET In-Person Instruction North America Rockville, MD, United States
Clinical Statistics for Nonstatisticians Sep 15, 2014 ACPE, IACET In-Person Instruction North America Rockville, MD, United States
Global Regulatory Strategy and Drug Development in Asia-Pacific, Latin America and Other Emerging Markets Sep 15, 2014 IACET In-Person Instruction North America Rockville, MD, United States
EudraVigilance - electronic reporting of ICSRs in the EEA Sep 17, 2014 In-Person Instruction Europe Zagreb, Croatia (Hrvatska)
Complimentary - Moving Your Regulated Content Management Platform to the Cloud: Benefits & Barriers Sep 17, 2014 Online Instruction Global Online
DIA Biosimilars 2014 Sep 18, 2014 ACPE, IACET Meetings North America Washington, DC, United States
Clinical Project Management (Basic-Int) Sep 18, 2014 In-Person Instruction China Suzhou, China
Improving Efficiency Within the Current Regulatory System: Results of the Escher project Sep 18, 2014 Meetings Europe Brussels, Belgium
Regulatory Information Management (RIM) Sep 21, 2014 In-Person Instruction North America Washington, DC, United States
MetaTMF METRICS 101 Sep 21, 2014 In-Person Instruction North America Washington, DC, United States
Medical Approach in Diagnosis and Management of ADRs Sep 22, 2014 In-Person Instruction Europe Charenton Le Pont, Paris, France
EDM and ERS 2014 Sep 22, 2014 Meetings North America Washington, DC, United States
EudraVigilance - electronic reporting of ICSRs in the EEA Sep 22, 2014 In-Person Instruction Europe Paris, France
Clinical Project Management - Part I Sep 22, 2014 In-Person Instruction Europe Charenton Le Pont, Paris, France
Quality by Design - New Concepts for Chemical and Biotech Product Development and Optimisation Sep 22, 2014 In-Person Instruction Europe Vienna, Austria
8th Annual European Medical Information and Communications Conference Sep 23, 2014 Meetings Europe London, United Kingdom
Clinical Trials Workshop I - Translating the New Clinical Trials Regulation into Practice Sep 23, 2014 Meetings Europe London, United Kingdom
Strategies for Good Clinical Practice Audits Sep 23, 2014 IACET, RN Online Instruction Global Online
Diagnosis and Management of Drug-Induced Liver Injury (DILI) Sep 23, 2014 In-Person Instruction Europe Charenton Le Pont, Paris, France
Clinical Trials Workshop II - Translating the New Transparency Requirements into Practice Sep 24, 2014 Meetings Europe London, United Kingdom
11th Latin American Conference of Clinical Research Sep 25, 2014 Meetings LATIN AMERICA Monterrey, Mexico
eXtended EudraVigilance Medicinal Product Dictionary (XEVMPD) Sep 25, 2014 In-Person Instruction Europe Paris, France
Statistical Workshop 2014 Sep 25, 2014 Meetings China Wuhan, China
Introduction to Signal Detection and Data Mining Sep 29, 2014 IACET Online Instruction Global Online
EudraVigilance - electronic reporting of ICSRs in the EEA Oct 01, 2014 In-Person Instruction Europe London, United Kingdom
Pharmacovigilance and Risk Management Planning Oct 01, 2014 ACPE, IACET In-Person Instruction North America Toronto, ON, Canada
DIA Canadian Pharmacovigilance & Risk Management Oct 02, 2014 IACET Meetings North America Toronto, ON, Canada
EudraVigilance - Electronic reporting of ICSRs in the EEA Oct 06, 2014 In-Person Instruction Europe Madrid, Spain
Disruptive Innovation in Medical Information Oct 06, 2014 ACPE, IACET Online Instruction Global Online
Joint DIA/ICOS Cardio-Oncology Conference Oct 09, 2014 Meetings Europe Prague, Czech Republic
eXtended EudraVigilance Medicinal Product Dictionary (XEVMPD) Oct 09, 2014 In-Person Instruction Europe Madrid, Spain
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
EMA Excellence in Pharmacovigilance: Clinical trials and post-marketing Oct 13, 2014 In-Person Instruction Europe London, United Kingdom
Introduction to Health Technology Assessment (HTA) Oct 13, 2014 In-Person Instruction Europe Charenton Le Pont, Paris, France
How to prepare for your meeting with Health Authorities Oct 14, 2014 In-Person Instruction Europe Charenton Le Pont, Paris, France
Introduction to Pharmacovigilance and Rules for Expedited Reporting of Individual Case Safety Reports (ICSRs) in Europe Oct 14, 2014 In-Person Instruction Europe London, United Kingdom
Fact or Fiction: Legal Restrictions to Patient Engagement in Drug Development Oct 14, 2014 ACPE, IACET 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
EudraVigilance - electronic reporting of ICSRs in the EEA Oct 15, 2014 In-Person Instruction Europe London, United Kingdom
DIA 2014 9th Annual India Conference: The Future of Indian Health Care: Patients, Access and Innovation Oct 16, 2014 Meetings India Mumbai, India
Regulatory Affairs for Biologics Oct 19, 2014 IACET In-Person Instruction North America Irvine, CA, United States
Postmarketing Drug Safety and Pharmacovigilance Oct 20, 2014 ACPE, IACET In-Person Instruction North America Horsham, PA, United States
EudraVigilance - electronic reporting of ICSRs in the EEA Oct 20, 2014 In-Person Instruction Europe San Marino, San Marino
ICH endorsed PhV training course Oct 21, 2014 In-Person Instruction Europe Dakar, Senegal
Global CTD Dossier – Regulatory aspects and focus on quality documentation including concepts of Quality by Design Oct 21, 2014 In-Person Instruction Europe Dakar, Senegal
Adaptive Design in Clinical Trials: When and How to Apply Oct 21, 2014 In-Person Instruction North America Philadelphia, PA, United States
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 IACET Online Instruction Global Online
4th African Regulatory Conference (ARC) Oct 22, 2014 Meetings Europe Dakar, Senegal
Practical GCP Compliance Auditing of Trials and Systems Oct 22, 2014 In-Person Instruction Europe London, United Kingdom
Biopharmaceuticals, Biosimilars and Advanced Therapies - Development and Regulatory Framework in Europe Oct 22, 2014 In-Person Instruction Europe London, United Kingdom
Clinical Statistics for Non-Statisticians Oct 23, 2014 In-Person Instruction Europe London, United Kingdom
5th DIA Cardiac Safety Workshop in Japan Oct 23, 2014 Meetings Japan Tokyo, Japan
4th DIA Project Management Training Course in Japan Oct 27, 2014 In-Person Instruction Japan Tokyo, Japan
Biostatistics for Non-Statisticians Oct 27, 2014 IACET In-Person Instruction North America
Risk Management Plans and Drug Utilization Studies in Canada Oct 27, 2014 IACET In-Person Instruction North America Ottawa, ON, Canada
DIA’s Annual Canadian Meeting: Thinking Globally, Acting Locally for The Well-Being of the Patient Oct 28, 2014 Meetings North America Ottawa, ON, Canada
Combination Products: A Comprehensive Overview of Premarket Opportunities and Postmarket Challenges! Oct 28, 2014 In-Person Instruction North America Washington, DC, United States
Patient Engagement throughout the Full Spectrum of Drug Development: An Interactive Workshop for Life Science Companies and Patient Groups Oct 29, 2014 IACET Meetings North America Washington, DC, United States
DIA Meeting on Combination Products Oct 29, 2014 IACET Meetings North America Washington, DC, United States
DIA Meeting on Companion Diagnostics Oct 30, 2014 IACET Meetings North America Washington, DC, United States
Negotiation and Influence Oct 30, 2014 IACET, PMI Online Instruction Global Online
Quantitative Science Forum Oct 31, 2014 Meetings China Beijing, China
Navigating Chemistry, Manufacturing & Controls Through the Drug Development Process Nov 03, 2014 IACET In-Person Instruction North America Horsham, PA, United States
How to Prepare for Pharmacovigilance Audits and Inspections Nov 03, 2014 In-Person Instruction Europe Charenton Le Pont, Paris, France
Advanced Signal Detection - Tools, Triage, Evaluation, and Escalation Nov 03, 2014 IACET In-Person Instruction North America Washington, DC, United States
Essentials of European Regulatory Affairs Nov 03, 2014 In-Person Instruction Europe Charenton Le Pont, Paris, France
Signal Management in Pharmacovigilance Nov 03, 2014 In-Person Instruction Europe Charenton Le Pont, Paris, France
Introduction to Pharmacovigilance and Rules for Expedited Reporting of Individual Case Safety Reports (ICSRs) in Europe Nov 04, 2014 In-Person Instruction Europe London, United Kingdom
Essentials of Clinical Study Management Nov 05, 2014 In-Person Instruction Europe London, United Kingdom
US Regulatory Affairs Nov 05, 2014 In-Person Instruction Europe London, United Kingdom
EudraVigilance - electronic reporting of ICSRs in the EEA Nov 05, 2014 In-Person Instruction Europe London, United Kingdom
ISPE/DIA Workshop on Computer Systems Compliance “Maintain Data Integrity to Reduce Risk for the Patient” Nov 06, 2014 Meetings Europe Basel, Switzerland
Tutorial 1: From the Pediatric Case Files of FDA Nov 06, 2014 IACET In-Person Instruction North America North Bethesda, MD, United States
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
Pediatric Research Conference 2014: Transforming the Pediatric Research Landscape through Innovation and Forward Thinking Nov 06, 2014 IACET Meetings North America North Bethesda, MD, United States
Electronic Submissions: The Next Era of Electronic Submissions Nov 09, 2014 IACET In-Person Instruction North America Bethesda, MD, United States
Benefit/Risk Management Nov 10, 2014 In-Person Instruction Europe Barcelona, Spain
Clinical Project Management Part II Nov 10, 2014 In-Person Instruction Europe Barcelona, Spain
Regulatory Affairs: The IND, NDA, and Postmarketing Nov 10, 2014 IACET In-Person Instruction North America Bethesda, MD, United States
The Leadership Experience Nov 10, 2014 IACET, PMI In-Person Instruction North America Bethesda, MD, United States
Risk Management and Safety Communication Strategies Nov 10, 2014 ACPE, IACET In-Person Instruction North America Bethesda, MD, United States
Joint DIA/AEMPS Statistics Workshop Nov 10, 2014 Meetings Europe Barcelona, Spain
EudraVigilance - electronic reporting of ICSRs in the EEA Nov 10, 2014 In-Person Instruction Europe Vienna, Austria
Optimizing Financial Management to Maximize Clinical Trial Investments Nov 11, 2014 Meetings North America Philadelphia, PA, United States
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 IACET Online Instruction Global Online
#1 Basic Introduction for Non-Specialist: Drug-Drug Interaction and Summary of Change in New Japanese Drug-Drug Interaction Guideline Nov 16, 2014 In-Person Instruction Japan Tokyo, Japan
#2 Next Steps for Content of Company Core Data Sheet Prepared by Western Companies - Part 1 Nov 16, 2014 In-Person Instruction Japan Tokyo, Japan
#3 Action Learning for Six Sigma Analytical Tools Using Real Case Studies Nov 16, 2014 In-Person Instruction Japan Tokyo, Japan
#4 Coaching as a Diverse Communication Tool Across Functions and Areas Nov 16, 2014 In-Person Instruction Japan Tokyo, Japan
#5 The Basics of “Investigator Initiated Trial (IIT)” Regulation Nov 16, 2014 In-Person Instruction Japan Tokyo, Japan
11th Annual Meeting DIA Japan 2014 Nov 16, 2014 Meetings Japan Tokyo, Japan
#6 Prediction for Human Pharmacokinetics and Safety Using Systems Pharmacology Nov 16, 2014 In-Person Instruction Japan Tokyo, Japan
#7 Next Steps for Content of Company Core Data Sheet Prepared by Western Companies - Part 2 Nov 16, 2014 In-Person Instruction Japan Tokyo, Japan
#8 An Introduction to Adaptive Designs Nov 16, 2014 In-Person Instruction Japan Tokyo, Japan
#9 Let’s Learn and Talk about Project Management Basics of the Clinical Study in Medical Institutes! Nov 16, 2014 In-Person Instruction Japan Tokyo, Japan
#10 HTA 2016? What are the challenges for Japan? Nov 16, 2014 In-Person Instruction Japan Tokyo, Japan
Special DIA Japan 2014 Sunday Pass: Buy Pre-Conference Tutorial(s) and Stay for Afternoon Plenary/Special Sessions Nov 16, 2014 Meetings Japan Tokyo, Japan
EudraVigilance - electronic reporting of ICSRs in the EEA Nov 17, 2014 In-Person Instruction Europe London, United Kingdom
Special DIA Japan 2014 Medical Device Pass: Attend [V6-S6] and Stay through Closing Sessions Nov 18, 2014 Meetings Japan Tokyo, Japan
eXtended EudraVigilance Medicinal Product Dictionary (XEVMPD) Nov 20, 2014 In-Person Instruction Europe London, United Kingdom
1st Maghreb Regulatory Conference Nov 24, 2014 Meetings Europe Algiers, Algeria
ICH endorsed PhV training course Nov 26, 2014 In-Person Instruction Europe Algiers, Algeria
EudraVigilance - electronic reporting of ICSRs in the EEA Nov 26, 2014 In-Person Instruction Europe Lisboa, Portugal
15th Annual Conference on Electronic Document Management (eDM) Dec 02, 2014 Meetings Europe Berlin, Germany
Biosimilars Conference Dec 02, 2014 Meetings Europe Berlin, Germany
EudraVigilance - electronic reporting of ICSRs in the EEA Dec 03, 2014 In-Person Instruction Europe London, United Kingdom
Joint MHRA/EMA/MSSO Information Day MedDRA in the Pharmacovigilance Regulatory Process Dec 08, 2014 In-Person Instruction Europe London, United Kingdom
Preparation of a Successful (CTD) with Quality by Design (QbD) Dec 08, 2014 In-Person Instruction China
2nd DIA Advanced Regulatory Affairs Training Course in Japan Dec 08, 2014 In-Person Instruction Japan Tokyo, Japan
FDA IND/NDA Workshop Dec 11, 2014 Meetings China Beijing, China
Pharmacovigilance and Risk Management Strategies 2015 Jan 26, 2015 Meetings North America Washington, DC, United States
18th Annual Workshop in Japan for Clinical Data Management Jan 29, 2015 Meetings Japan Tokyo, Japan
Joint Adaptive Design and Bayesian Statistics Conference: Drivers of Efficiency in Modern Medical Product Development Feb 10, 2015 Meetings North America Arlington, VA, United States
Marketing Pharmaceuticals 2015 Feb 17, 2015 Meetings North America Washington, DC, United States
CMC Workshop 2015 Apr 13, 2015 Meetings North America Bethesda, MD, United States
8th Annual Clinical Forum Apr 13, 2015 Meetings Europe Paris, France
27th Annual EuroMeeting Apr 13, 2015 Meetings Europe Paris, France
DIA China 2014 7th Annual Meeting May 24, 2015 Meetings China Shanghai, China
DIA 2015 51st Annual Meeting: Develop. Innovate. Advance. Jun 14, 2015 Meetings North America Washington, DC, United States