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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
Clinical Investigator: Module 2 - Conducting The Study Oct 26, 2014 ACPE, CME Online Instruction North America Online
Clinical Investigator: Module 1 - Study Preparation and Initiation Oct 26, 2014 ACPE, CME Online Instruction North America Online
Informed Consent Oct 26, 2014 ACPE Online Instruction North America Online
Crisis Management Oct 26, 2014 ACPE, IACET Online Instruction North America Online
Database Management Oct 26, 2014 ACPE, IACET Online Instruction North America Online
Literature Evaluation Oct 26, 2014 ACPE, IACET Online Instruction North America Online
Literature Searching Oct 26, 2014 ACPE, IACET Online Instruction North America Online
Medical Inquiries Oct 26, 2014 ACPE, IACET Online Instruction North America Online
Medical Writing Oct 26, 2014 IACET Online Instruction North America Online
Product Labeling Oct 26, 2014 ACPE, IACET Online Instruction North America Online
Regulatory Issues Oct 26, 2014 ACPE, IACET Online Instruction North America Online
Statistics for Medical Communications Professionals Oct 26, 2014 ACPE, IACET Online Instruction North America Online
The Use of Mobile Medical Applications as Companions Oct 26, 2014 Online Instruction Global Online
Generic Drug Labeling Proposed Rule and Safety Updates Oct 26, 2014 Online Instruction Global Online
Emerging Technologies to Rare Disorder Drug Development: Promises and Pitfalls Oct 26, 2014 Online Instruction Global Online
Big Data: Impact of Health Care Reform on Collaborations and Strategies Oct 26, 2014 Online Instruction Global Online
The Role of the Clinical Data Manager Oct 26, 2014 Online Instruction Global Online
Implementation of the FDASIA Patient Provisions Oct 26, 2014 Online Instruction Global Online
Complimentary: Regulatory and Real World Evidence Challenges of Rare Diseases and Orphan Drugs Oct 26, 2014 Online Instruction Global Online
Variations in the European Union: CMC/Quality Changes Oct 26, 2014 Online Instruction Global Online
Good Pharmacovigilance Practice: How Good has it Proven to be for Industry? Oct 26, 2014 Online Instruction Global Online
Pharmacovigilance and Risk Management: Patient Perspective Oct 26, 2014 Online Instruction Global Online
Complimentary Patient-Centeredness and Engagement in Clinical Research: Opportunities for Industry Oct 26, 2014 Online Instruction Global Online
Drug Safety Regulatory Requirements Oct 26, 2014 ACPE, IACET Online Instruction Global Online
Premarketing Clinical Trial Safety Oct 26, 2014 ACPE, IACET Online Instruction Global Online
Postmarketing Safety Management Oct 26, 2014 ACPE, IACET Online Instruction Global Online
Basics of Signal Detection and Pharmacoepidemiology Oct 26, 2014 ACPE, IACET Online Instruction Global Online
Safety Audits and Inspections Oct 26, 2014 Online Instruction Global Online
Five-Part Series on Fundamentals of Clinical Pharmacology for Drug Development - Part 1: Fundamentals of Clinical Pharmacology: Pharmacokinetics Oct 26, 2014 Online Instruction Global Online
Five-Part Series on Fundamentals of Clinical Pharmacology for Drug Development - Part 2: Fundamentals of Clinical Pharmacology: Pharmacodynamics Oct 26, 2014 Online Instruction Global Online
Pharmacovigilance and Global Harmonization Updates Oct 26, 2014 Online Instruction Global Online
Five-Part Series on Fundamentals of Clinical Pharmacology For Drug Development - Part 3: Principles of Modeling and Simulation Oct 26, 2014 Online Instruction Global Online
Five-Part Series on Fundamentals of Clinical Pharmacology for Drug Development - Part 4: Determining the Safe First Human Dose Oct 26, 2014 Online Instruction Global Online
Designed for Success: Utilizing Protocol Quality by Design (QbD) to Plan Clinical Studies Oct 26, 2014 Online Instruction Global Online
Negotiation and Influence Oct 26, 2014 Online Instruction Global Online
China Update: Regulatory Changes and Implications Oct 26, 2014 Online Instruction Global Online
Evaluation and Management of Cardiac Conditions in Oncology Patients Oct 26, 2014 Online Instruction Global Online
Risk Management of Medicinal Products: REMS and RMP - Need for Harmonization Within the ICH Region? Oct 26, 2014 Online Instruction Global Online
Introduction to Drug Safety Oct 26, 2014 ACPE, IACET Online Instruction Global Online
How to Prepare for a Safety Inspection Oct 26, 2014 Online Instruction Global Online
Clinical Statistics for Nonstatisticians Oct 26, 2014 Online Instruction Global Online
Advanced Clinical Statistics for Nonstatisticians Oct 26, 2014 Online Instruction Global Online
Development of a Clinical Study Report Oct 26, 2014 Online Instruction Global Online
Art of Writing a Clinical Overview Oct 26, 2014 Online Instruction Global Online
CardioVascular Safety: The New Paradigm - Proarrhythmic Assessment of New Drugs without the Thorough QT Study Oct 26, 2014 Online Instruction Global Online
CardioVascular Safety – What are the Key Issues Regarding Blood Pressure Assessment During Clinical Development Oct 26, 2014 Online Instruction Global Online
Introductory Principles and Application of Risk Management within Clinical Operations Oct 26, 2014 Online Instruction Global Online
Seven-Part Series on Pediatric Drug Development - Part 6: Preclinical Toxicology & Safety Oct 26, 2014 Online Instruction Global Online
Electronic Submissions 101 – Essential MS Word and Adobe Acrobat Tools/Skills and Current IT Options Oct 26, 2014 Online Instruction Global Online
Disruptive Innovation in Medical Information Oct 26, 2014 Online Instruction Global Online
A Tour of FDA Oct 26, 2014 Online Instruction Global Online
A Tour of Health Canada Oct 26, 2014 Online Instruction Global Online
A Tour of Health Europe Oct 26, 2014 Online Instruction Global Online
Aspects of Regulatory History Oct 26, 2014 Online Instruction Global Online
Bioresearch Monitoring Program (BIMO): Introduction Oct 26, 2014 Online Instruction Global Online
The Clinical Development Process: Investigational Product, Plan, and Data Management Oct 26, 2014 Online Instruction Global Online
Drug Safety & Adverse Event Reporting Oct 26, 2014 Online Instruction Global Online
Ethical Review Boards Oct 26, 2014 Online Instruction Global Online
Ethics as the Foundation to Clinical Research Oct 26, 2014 Online Instruction Global Online
Awareness of FDA Inspections for Pharmaceutical Manufacturers Oct 26, 2014 Online Instruction Global Online
Biotechnology: An Overview of Compliance Considerations Oct 26, 2014 Online Instruction Global Online
Change Control Oct 26, 2014 Online Instruction Global Online
Clinical Trial Audits and Consequences of Non-Compliance Oct 26, 2014 Online Instruction Global Online
Computerized Systems Inspections in the Medical Device Industry Oct 26, 2014 Online Instruction Global Online
European Union Clinical Trials Directive Oct 26, 2014 Online Instruction Global Online
GMP Principals of SOPs Oct 26, 2014 Online Instruction Global Online
GMP Updates - Enforcement Changes at the New FDA Oct 26, 2014 Online Instruction Global Online
GMPs for API Bulk Manufacturers Oct 26, 2014 Online Instruction Global Online
Good Clinical Practices (GCPs) for New Product Investigations Oct 26, 2014 Online Instruction Global Online
Good Laboratory Practices (GLPs) Oct 26, 2014 Online Instruction Global Online
GxPs Oct 26, 2014 Online Instruction Global Online
HIPAA - The Impact on Clinical Research Oct 26, 2014 Online Instruction Global Online
Introduction to GMPs Oct 26, 2014 Online Instruction Global Online
Investigational Product Development Oct 26, 2014 Online Instruction Global Online
ISO 14155: Obligations of Sponsors and Monitors for Medical Device Trials Oct 26, 2014 Online Instruction Global Online
Key Concepts of Process Validation Oct 26, 2014 Online Instruction Global Online
Laboratory Specimens for Clinical Research Oct 26, 2014 Online Instruction Global Online
Medical Device Safety Reporting Oct 26, 2014 Online Instruction Global Online
Orientation to GMP Compliance Oct 26, 2014 Online Instruction Global Online
Overview of the Clinical Research Process Oct 26, 2014 Online Instruction Global Online
Part 11: Electronic Records and Signatures - Application Oct 26, 2014 Online Instruction Global Online
Part 11: Electronic Records; Electronic Signatures Oct 26, 2014 Online Instruction Global Online
Principles of Good Documentation Oct 26, 2014 Online Instruction Global Online
Protection of Human Subjects in Clinical Trials Oct 26, 2014 Online Instruction Global Online
Selecting and Managing Clinical Contract Research Organizations (CROs) Oct 26, 2014 Online Instruction Global Online
Understanding Post-Approval Changes Oct 26, 2014 Online Instruction Global Online
Computerized Systems Inspections in the Pharmaceutical Industry Oct 26, 2014 Online Instruction Global Online
Basics of the PhRMA Code Oct 26, 2014 Online Instruction Global Online
Basics of AdvaMed Code Oct 26, 2014 Online Instruction Global Online
Eucomed Guidelines on Interactions with Healthcare Professionals Oct 26, 2014 Online Instruction Global Online
Introduction to Medical Device Health Care Compliance Oct 26, 2014 Online Instruction Global Online
Foreign Corrupt Practices Act Oct 26, 2014 Online Instruction Global Online
Global Anti-bribery Oct 26, 2014 Online Instruction Global Online
Variations to Marketing Authorisation in Europe Oct 26, 2014 Online Instruction Global Online
Registration of Monoclonal Antibodies Oct 26, 2014 Online Instruction Global Online
How to Gain Approval to Market a Generic Medicinal Product in the USA Oct 26, 2014 Online Instruction Global Online
Pharmacokinetics and Pharmacodynamics in Drug Registration Oct 26, 2014 Online Instruction Global Online
Complimentary - Press the Easy Button – Ensure Consistency and Compliance for your Documents through Automation Oct 26, 2014 Online Instruction Global Online
Complimentary - When Outsourcing Stops Making Sense Oct 26, 2014 Online Instruction Global Online
Complimentary Quintiles/DIA Webinar - Giving Your Study The Right Start Toward Success Through Optimal Country and Site Selection Oct 26, 2014 Online Instruction Global Online
Complimentary - Risk-Based Monitoring: Regulatory Expectation and Operational Application Oct 26, 2014 Online Instruction Global Online
Fundamentals of Project Management for Nonproject Managers Oct 26, 2014 Online Instruction Global Online
Planning and Managing Your Projects Oct 26, 2014 Online Instruction Global Online
Project Risk Management: Dealing with the Certainty of Uncertainty Oct 26, 2014 Online Instruction Global Online
Team Building and Development Oct 26, 2014 Online Instruction Global Online
Preparing a Clinical Trial Budget Oct 26, 2014 Online Instruction Global Online
Team Building and Development Oct 26, 2014 Online Instruction Global Online
Introduction to the European Union Institutions and Regulatory Authority Oct 26, 2014 Online Instruction Global Online
Introduction to US Institutions and Regulatory Authority (FDA) Oct 26, 2014 Online Instruction Global Online
Introduction to Japanese Institutions and Regulatory Authorities Oct 26, 2014 Online Instruction Global Online
Overview of the CTD and eCTD Oct 26, 2014 Online Instruction Global Online
Introduction to the International Conference on Harmonisation (ICH) Oct 26, 2014 Online Instruction Global Online
The Regulatory Development of a Drug Oct 26, 2014 Online Instruction Global Online
Basics of Clinical Trials Oct 26, 2014 Online Instruction Global Online
How to Register Medicinal Products through the Centralized Procedure Oct 26, 2014 Online Instruction Global Online
How to Register Medicinal Products through the Mutual Recognition Procedure Oct 26, 2014 Online Instruction Global Online
How to Maintain Marketing Approvals in Europe for Centrally Authorised Products Oct 26, 2014 Online Instruction Global Online
How to Register a New Drug in the USA Oct 26, 2014 Online Instruction Global Online
How to Register Medicinal Products through the Decentralized Procedure Oct 26, 2014 Online Instruction Global Online
Access to Unapproved Drugs through Compassionate Use Oct 26, 2014 Online Instruction Global Online
Regulatory Requirements for the Conduct of Clinical Trials in Europe Oct 26, 2014 Online Instruction Global Online
Orphan Drugs in the USA, European Union, and Japan Oct 26, 2014 Online Instruction Global Online
Regulatory Requirements for the Submission of Investigational New Drug Applications in the USA (INDs) Oct 26, 2014 Online Instruction Global Online
Meeting Opportunities with Regulatory Agencies Oct 26, 2014 Online Instruction Global Online
Combination Products and Convergence: An Overview of Clinical Benefits, Regulatory Issues & Manufacturing Challenges Oct 26, 2014 Online Instruction Global Online
Regulatory Solutions in the Cloud - 10 Questions You Can't Afford NOT to Ask Oct 26, 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 Oct 26, 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 Oct 26, 2014 Online Instruction Global Online
Strategies for Successfully Introducing REMS to Your Organization: From Development and Implementation and Internal and External Evaluation Oct 26, 2014 Online Instruction Global Online
The Case of the New England Compounding Center: Learning from the Tragedy Oct 26, 2014 Online Instruction Global Online
Complimentary - From the Clinic to the CFO: Adaptive Trials and Financial Decision-Making Oct 26, 2014 Online Instruction Global Online
Adverse Event Reporting Requirements: IND and Postmarketing Oct 26, 2014 Online Instruction Global Online
Complimentary - The Affiliate Challenge – How to Improve Compliance and Efficiency when Working with Regional Affiliates Oct 26, 2014 Online Instruction Global Online
The Future of Personalized Medicine and Companion Diagnostics Oct 26, 2014 Online Instruction Global Online
Seven-Part Series on Pediatric Drug Development - Part 1: Overall Challenge: The Vision of Better Medicines for Children Oct 26, 2014 Online Instruction Global Online
Seven-Part Series on Pediatric Drug Development - Part 3: Regulatory Framework EU Oct 26, 2014 Online Instruction Global Online
Seven-Part Pediatric Drug Development Webinar Series - Part 4: Dosing in Children Oct 26, 2014 Online Instruction Global Online
Seven-Part Series on Pediatric Drug Development - Part 2: Regulatory Framework US Overview Oct 26, 2014 Online Instruction Global Online
Seven-Part Series on Pediatric Drug Development - Part 5: Technical Development: Pediatric Formulations Oct 26, 2014 Online Instruction Global Online
Basics of the IND Oct 26, 2014 Online Instruction Global Online
Basics of the NDA Oct 26, 2014 Online Instruction Global Online
Regulatory Aspects of Prescription Drug/Biologics Advertising and Promotional Labeling Oct 26, 2014 Online Instruction Global Online
Seven-Part Series on Pediatric Drug Development - Part 7: Operational Challenges of Pediatric Clinical Trials Oct 26, 2014 Online Instruction Global Online
The Current State of Quality Oversight (QO) in the Pharmaceutical Industry Oct 26, 2014 Online Instruction Global Online
Supplements and Other Changes to an Approved Application Oct 26, 2014 Online Instruction Global Online
4th DIA Project Management Training Course in Japan Oct 27, 2014 PMI In-Person Instruction Japan Tokyo, Japan
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 ACPE, IACET Meetings North America Ottawa, ON, Canada
Combination Products: A Comprehensive Overview of Premarket Opportunities and Postmarket Challenges! Oct 28, 2014 IACET In-Person Instruction North America Washington, DC, United States
How New Electronic Trial Master File (eTMF) Data Standards Can Enhance Clinical Trial Efficiency and Quality Oct 28, 2014 Online Instruction Global Online
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
Complimentary Tutorial: Competing Regulatory Oversight of Investigational Tests, including LDTs, for Co-Development Programs Oct 29, 2014 In-Person Instruction 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
Multicentre International Data Integrity Workshop (Mumbai) Nov 03, 2014 In-Person Instruction India Andheri East, MH, India
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
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
Multicentre International Data Integrity Workshop (Mumbai) Nov 06, 2014 In-Person Instruction India Andheri East, MH, India
ISPE/DIA Workshop on Computer Systems Compliance “Maintain Data Integrity to Reduce Risk for the Patient” Nov 06, 2014 Meetings Europe Basel, Switzerland
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
Multicentre International Data Integrity Workshop (Hyderabad) Nov 10, 2014 In-Person Instruction India Hyderabad, India
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
Tutorial: AN INTRODUCTION TO THE JOINT MODELLING OF LONGITUDINAL AND SURVIVAL DATA Nov 10, 2014 In-Person Instruction Europe Barcelona, Spain
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
Multicentre International Data Integrity Workshop (Bangalore) Nov 13, 2014 In-Person Instruction India Bangalore, India
11th Annual Meeting DIA Japan 2014 Nov 16, 2014 Meetings Japan Tokyo, Japan
#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
#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
Proarrhythmia Nov 19, 2014 ACPE, IACET Online Instruction Global Online
eXtended EudraVigilance Medicinal Product Dictionary (XEVMPD) Nov 20, 2014 In-Person Instruction Europe London, United Kingdom
FDA IND/NDA Workshop Nov 20, 2014 Meetings China Beijing, China
Need to Reinvent the Clinical Trial? Innovate, Collaborate & Integrate Nov 20, 2014 Online Instruction Global Online
Impact on Drug Development of Novel Translational Safety Biomarkers for Improved Detection of Drug-Induced Acute Kidney Injury Nov 20, 2014 ACPE, IACET Online Instruction Global Online
The 1st DIA China Drug Induced Cardiovascular Toxicity Workshop Nov 23, 2014 Meetings China
EudraVigilance - electronic reporting of ICSRs in the EEA Nov 26, 2014 In-Person Instruction Europe Lisboa, Portugal
Tutorial 01:ELECTRONIC TRIAL MASTER FILES (eTMF) - MOVING FROM IMPLEMENTATION TO PROJECT EXCELLENCE Dec 01, 2014 In-Person Instruction Europe Berlin, Germany
Tutorial 02: UNDERSTANDING THE IMPACT OF IDENTIFICATION OF MEDICINAL PRODUCTS (IDMP) ON PROCESSES, DATA PROVISION, GOVERNANCE AND IT ARCHITECTURE Dec 01, 2014 In-Person Instruction Europe Berlin, Germany
15th Annual Conference on Electronic Document Management (eDM) Dec 02, 2014 Meetings Europe Berlin, Germany
Biosimilars Conference Dec 02, 2014 Meetings Europe Berlin, Germany
Target Product Profile – Strategies to Optimize Drug Development, Product Labeling, and Commercialization Dec 02, 2014 Online Instruction Global Online
The Basics of Clinical Data Management From Start to End Dec 03, 2014 IACET In-Person Instruction North America Washington, DC, United States
EudraVigilance - electronic reporting of ICSRs in the EEA Dec 03, 2014 In-Person Instruction Europe London, United Kingdom
Facets of Drug-Induced Kidney Injury and Regulatory Perspective Dec 03, 2014 ACPE, IACET Online Instruction Global Online
Cardio-Oncology: Innovative Strategies for Mitigating Cardiovascular Risk of New Cancer Therapies Dec 04, 2014 Online Instruction Global Online
Joint MHRA/MedDRA 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
3rd DIA Statistics Workshop for all Clinical Research Professionals in Japan Dec 09, 2014 Meetings Japan Tokyo, Japan
Implementation and Status of Periodic Benefit-Risk Evaluation Reporting (PBRER) in Canada Dec 09, 2014 Online Instruction Global Online
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
1st Maghreb Regulatory Conference Feb 10, 2015 Meetings Europe Algiers, Algeria
ICH endorsed PhV training course Feb 12, 2015 In-Person Instruction Europe Algiers, Algeria
Marketing Pharmaceuticals 2015: Drug/Device Marketing in an Evolving Environment Feb 17, 2015 Meetings North America Washington, DC, United States
Benefit/Risk Management Mar 10, 2015 In-Person Instruction Europe Hamburg, Germany
Essentials of European Regulatory Affairs Mar 10, 2015 In-Person Instruction Europe Hamburg, Germany
3rd DIA Clinical Operation & Monitoring Workshop in Japan Mar 12, 2015 Meetings Japan Tokyo, Japan
Medical & Scientific Communications 2015 Annual Forum Mar 16, 2015 Meetings North America Glendale, AZ, 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/FDA Statistics Forum 2015 Apr 20, 2015 Meetings North America North Bethesda, MD, United States
Global CTD Dossier – Regulatory aspects and focus on quality documentation including concepts of Quality by Design Apr 26, 2015 In-Person Instruction Europe Dakar, Senegal
ICH endorsed PhV training course Apr 26, 2015 In-Person Instruction Europe Dakar, Senegal
4th African Regulatory Conference (ARC) Apr 27, 2015 Meetings Europe Dakar, Senegal
Signal Management in Pharmacovigilance Apr 27, 2015 In-Person Instruction Europe Basel, Switzerland
How to prepare for Pharmacovigilance Audits and Inspections Apr 28, 2015 In-Person Instruction Europe Basel, Switzerland
eRegulatory and Intelligence Annual Conference May 11, 2015 Meetings North America
7th DIA China Annual Meeting May 24, 2015 Meetings China Shanghai, China
Medical Approach in Diagnosis and Management of ADRs Jun 10, 2015 In-Person Instruction Europe Charenton Le Pont, Paris, France
Diagnosis and Management of Drug-Induced Liver Injury (DILI) Jun 11, 2015 In-Person Instruction Europe Charenton Le Pont, Paris, France
DIA 2015 51st Annual Meeting: Develop. Innovate. Advance. Jun 14, 2015 Meetings North America Washington, DC, United States
Paediatric Investigation Plans (PIP) Sep 17, 2015 In-Person Instruction Europe London, United Kingdom
Good Managament of Medical Devices Sep 21, 2015 In-Person Instruction Europe Vienna, Austria