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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 Jan 26, 2015 ACPE, CME Online Instruction North America Online
Clinical Investigator: Module 1 - Study Preparation and Initiation Jan 26, 2015 ACPE, CME Online Instruction North America Online
Informed Consent Jan 26, 2015 ACPE Online Instruction North America Online
Crisis Management Jan 26, 2015 ACPE, IACET Online Instruction North America Online
Database Management Jan 26, 2015 ACPE, IACET Online Instruction North America Online
Literature Evaluation Jan 26, 2015 ACPE, IACET Online Instruction North America Online
Literature Searching Jan 26, 2015 ACPE, IACET Online Instruction North America Online
Medical Inquiries Jan 26, 2015 ACPE, IACET Online Instruction North America Online
Medical Writing Jan 26, 2015 IACET Online Instruction North America Online
Product Labeling Jan 26, 2015 ACPE, IACET Online Instruction North America Online
Regulatory Issues Jan 26, 2015 ACPE, IACET Online Instruction North America Online
Statistics for Medical Communications Professionals Jan 26, 2015 ACPE, IACET Online Instruction North America Online
The Use of Mobile Medical Applications as Companions Jan 26, 2015 Online Instruction Global Online
Generic Drug Labeling Proposed Rule and Safety Updates Jan 26, 2015 Online Instruction Global Online
Emerging Technologies to Rare Disorder Drug Development: Promises and Pitfalls Jan 26, 2015 Online Instruction Global Online
Target Product Profile – Strategies to Optimize Drug Development, Product Labeling, and Commercialization Jan 26, 2015 Online Instruction Global Online
The Role of the Clinical Data Manager Jan 26, 2015 Online Instruction Global Online
Implementation of the FDASIA Patient Provisions Jan 26, 2015 Online Instruction Global Online
Complimentary: Regulatory and Real World Evidence Challenges of Rare Diseases and Orphan Drugs Jan 26, 2015 Online Instruction Global Online
Variations in the European Union: CMC/Quality Changes Jan 26, 2015 Online Instruction Global Online
Proarrhythmia Jan 26, 2015 Online Instruction Global Online
Facets of Drug-Induced Kidney Injury and Regulatory Perspective Jan 26, 2015 Online Instruction Global Online
Impact on Drug Development of Novel Translational Safety Biomarkers for Improved Detection of Drug-Induced Acute Kidney Injury Jan 26, 2015 Online Instruction Global Online
Pharmacovigilance and Risk Management: Patient Perspective Jan 26, 2015 Online Instruction Global Online
Complimentary Patient-Centeredness and Engagement in Clinical Research: Opportunities for Industry Jan 26, 2015 Online Instruction Global Online
Drug Safety Regulatory Requirements Jan 26, 2015 ACPE, IACET Online Instruction Global Online
Premarketing Clinical Trial Safety Jan 26, 2015 ACPE, IACET Online Instruction Global Online
Postmarketing Safety Management Jan 26, 2015 ACPE, IACET Online Instruction Global Online
Basics of Signal Detection and Pharmacoepidemiology Jan 26, 2015 ACPE, IACET Online Instruction Global Online
Safety Audits and Inspections Jan 26, 2015 ACPE, IACET Online Instruction Global Online
Five-Part Series on Fundamentals of Clinical Pharmacology for Drug Development - Part 1: Fundamentals of Clinical Pharmacology: Pharmacokinetics Jan 26, 2015 Online Instruction Global Online
Five-Part Series on Fundamentals of Clinical Pharmacology for Drug Development - Part 2: Fundamentals of Clinical Pharmacology: Pharmacodynamics Jan 26, 2015 Online Instruction Global Online
Pharmacovigilance and Global Harmonization Updates Jan 26, 2015 Online Instruction Global Online
Five-Part Series on Fundamentals of Clinical Pharmacology For Drug Development - Part 3: Principles of Modeling and Simulation Jan 26, 2015 Online Instruction Global Online
Five-Part Series on Fundamentals of Clinical Pharmacology for Drug Development - Part 4: Determining the Safe First Human Dose Jan 26, 2015 Online Instruction Global Online
Five-Part Series on Fundamentals of Clinical Pharmacology for Drug Development - Part 5: Assessment of QT Prolongation Jan 26, 2015 Online Instruction Global Online
Designed for Success: Utilizing Protocol Quality by Design (QbD) to Plan Clinical Studies Jan 26, 2015 Online Instruction Global Online
Negotiation and Influence Jan 26, 2015 Online Instruction Global Online
Introduction to Drug Safety Jan 26, 2015 ACPE, IACET Online Instruction Global Online
How to Prepare for a Safety Inspection Jan 26, 2015 Online Instruction Global Online
Implementation and Status of Periodic Benefit-Risk Evaluation Reporting (PBRER) in Canada Jan 26, 2015 Online Instruction Global Online
Clinical Statistics for Nonstatisticians Jan 26, 2015 Online Instruction Global Online
Advanced Clinical Statistics for Nonstatisticians Jan 26, 2015 Online Instruction Global Online
Development of a Clinical Study Report Jan 26, 2015 Online Instruction Global Online
Art of Writing a Clinical Overview Jan 26, 2015 Online Instruction Global Online
Introductory Principles and Application of Risk Management within Clinical Operations Jan 26, 2015 Online Instruction Global Online
Seven-Part Series on Pediatric Drug Development - Part 6: Preclinical Toxicology & Safety Jan 26, 2015 Online Instruction Global Online
Complimentary - Need to Reinvent the Clinical Trial? Innovate, Collaborate & Integrate Jan 26, 2015 Online Instruction Global Online
Disruptive Innovation in Medical Information Jan 26, 2015 Online Instruction Global Online
A Tour of FDA Jan 26, 2015 Online Instruction Global Online
A Tour of Health Canada Jan 26, 2015 Online Instruction Global Online
A Tour of Health Europe Jan 26, 2015 Online Instruction Global Online
Aspects of Regulatory History Jan 26, 2015 Online Instruction Global Online
Bioresearch Monitoring Program (BIMO): Introduction Jan 26, 2015 Online Instruction Global Online
The Clinical Development Process: Investigational Product, Plan, and Data Management Jan 26, 2015 Online Instruction Global Online
Ethical Review Boards Jan 26, 2015 Online Instruction Global Online
Ethics as the Foundation to Clinical Research Jan 26, 2015 Online Instruction Global Online
Awareness of FDA Inspections for Pharmaceutical Manufacturers Jan 26, 2015 Online Instruction Global Online
Biotechnology: An Overview of Compliance Considerations Jan 26, 2015 Online Instruction Global Online
Change Control Jan 26, 2015 Online Instruction Global Online
Clinical Trial Audits and Consequences of Non-Compliance Jan 26, 2015 Online Instruction Global Online
Computerized Systems Inspections in the Medical Device Industry Jan 26, 2015 Online Instruction Global Online
European Union Clinical Trials Directive Jan 26, 2015 Online Instruction Global Online
GMP Principals of SOPs Jan 26, 2015 Online Instruction Global Online
GMP Updates - Enforcement Changes at the New FDA Jan 26, 2015 Online Instruction Global Online
GMPs for API Bulk Manufacturers Jan 26, 2015 Online Instruction Global Online
Good Clinical Practices (GCPs) for New Product Investigations Jan 26, 2015 Online Instruction Global Online
Good Laboratory Practices (GLPs) Jan 26, 2015 Online Instruction Global Online
GxPs Jan 26, 2015 Online Instruction Global Online
HIPAA - The Impact on Clinical Research Jan 26, 2015 Online Instruction Global Online
Introduction to GMPs Jan 26, 2015 Online Instruction Global Online
Investigational Product Development Jan 26, 2015 Online Instruction Global Online
ISO 14155: Obligations of Sponsors and Monitors for Medical Device Trials Jan 26, 2015 Online Instruction Global Online
Key Concepts of Process Validation Jan 26, 2015 Online Instruction Global Online
Laboratory Specimens for Clinical Research Jan 26, 2015 Online Instruction Global Online
Medical Device Safety Reporting Jan 26, 2015 Online Instruction Global Online
Orientation to GMP Compliance Jan 26, 2015 Online Instruction Global Online
Overview of the Clinical Research Process Jan 26, 2015 Online Instruction Global Online
Part 11: Electronic Records and Signatures - Application Jan 26, 2015 Online Instruction Global Online
Part 11: Electronic Records; Electronic Signatures Jan 26, 2015 Online Instruction Global Online
Principles of Good Documentation Jan 26, 2015 Online Instruction Global Online
Protection of Human Subjects in Clinical Trials Jan 26, 2015 Online Instruction Global Online
Selecting and Managing Clinical Contract Research Organizations (CROs) Jan 26, 2015 Online Instruction Global Online
Understanding Post-Approval Changes Jan 26, 2015 Online Instruction Global Online
Computerized Systems Inspections in the Pharmaceutical Industry Jan 26, 2015 Online Instruction Global Online
Basics of the PhRMA Code Jan 26, 2015 Online Instruction Global Online
Basics of AdvaMed Code Jan 26, 2015 Online Instruction Global Online
Eucomed Guidelines on Interactions with Healthcare Professionals Jan 26, 2015 Online Instruction Global Online
Introduction to Medical Device Health Care Compliance Jan 26, 2015 Online Instruction Global Online
Foreign Corrupt Practices Act Jan 26, 2015 Online Instruction Global Online
Global Anti-bribery Jan 26, 2015 Online Instruction Global Online
Variations to Marketing Authorisation in Europe Jan 26, 2015 Online Instruction Global Online
Registration of Monoclonal Antibodies Jan 26, 2015 Online Instruction Global Online
How to Gain Approval to Market a Generic Medicinal Product in the USA Jan 26, 2015 Online Instruction Global Online
Pharmacokinetics and Pharmacodynamics in Drug Registration Jan 26, 2015 Online Instruction Global Online
Complimentary Quintiles/DIA Webinar - Giving Your Study The Right Start Toward Success Through Optimal Country and Site Selection Jan 26, 2015 Online Instruction Global Online
Implementing Risk-Based Monitoring: Practical Approaches Jan 26, 2015 Online Instruction Global Online
Complimentary - Innovative Strategies for Developing Safer Cancer Therapies Jan 26, 2015 Online Instruction Global Online
Complimentary - Risk-Based Monitoring: Regulatory Expectation and Operational Application Jan 26, 2015 Online Instruction Global Online
Fundamentals of Project Management for Nonproject Managers Jan 26, 2015 Online Instruction Global Online
Planning and Managing Your Projects Jan 26, 2015 Online Instruction Global Online
Preparing a Clinical Trial Budget Jan 26, 2015 Online Instruction Global Online
Team Building and Development Jan 26, 2015 Online Instruction Global Online
Pricing, Economic, Reimbursement, Market Share (PERMS) Strategy: An Interactive Holistic Approach in Rare Diseases Jan 26, 2015 Online Instruction Global Online
Introduction to the European Union Institutions and Regulatory Authority Jan 26, 2015 Online Instruction Global Online
Introduction to US Institutions and Regulatory Authority (FDA) Jan 26, 2015 Online Instruction Global Online
Introduction to Japanese Institutions and Regulatory Authorities Jan 26, 2015 Online Instruction Global Online
Overview of the CTD and eCTD Jan 26, 2015 Online Instruction Global Online
Introduction to the International Conference on Harmonisation (ICH) Jan 26, 2015 Online Instruction Global Online
The Regulatory Development of a Drug Jan 26, 2015 Online Instruction Global Online
Basics of Clinical Trials Jan 26, 2015 Online Instruction Global Online
How to Register Medicinal Products through the Centralized Procedure Jan 26, 2015 Online Instruction Global Online
How to Register Medicinal Products through the Mutual Recognition Procedure Jan 26, 2015 Online Instruction Global Online
How to Maintain Marketing Approvals in Europe for Centrally Authorised Products Jan 26, 2015 Online Instruction Global Online
How to Register a New Drug in the USA Jan 26, 2015 Online Instruction Global Online
How to Register Medicinal Products through the Decentralized Procedure Jan 26, 2015 Online Instruction Global Online
Access to Unapproved Drugs through Compassionate Use Jan 26, 2015 Online Instruction Global Online
Regulatory Requirements for the Conduct of Clinical Trials in Europe Jan 26, 2015 Online Instruction Global Online
Orphan Drugs in the USA, European Union, and Japan Jan 26, 2015 Online Instruction Global Online
Regulatory Requirements for the Submission of Investigational New Drug Applications in the USA (INDs) Jan 26, 2015 Online Instruction Global Online
Meeting Opportunities with Regulatory Agencies Jan 26, 2015 Online Instruction Global Online
How New Electronic Trial Master File (eTMF) Data Standards Can Enhance Clinical Trial Efficiency and Quality Jan 26, 2015 Online Instruction Global Online
Complimentary - Regulatory Solutions in the Cloud - 10 Questions You Can't Afford NOT to Ask Jan 26, 2015 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 Jan 26, 2015 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 Jan 26, 2015 Online Instruction Global Online
Complimentary - From the Clinic to the CFO: Adaptive Trials and Financial Decision-Making Jan 26, 2015 Online Instruction Global Online
Adverse Event Reporting Requirements: IND and Postmarketing Jan 26, 2015 Online Instruction Global Online
Complimentary - The Affiliate Challenge – How to Improve Compliance and Efficiency when Working with Regional Affiliates Jan 26, 2015 Online Instruction Global Online
The Future of Personalized Medicine and Companion Diagnostics Jan 26, 2015 Online Instruction Global Online
Seven-Part Series on Pediatric Drug Development - Part 1: Overall Challenge: The Vision of Better Medicines for Children Jan 26, 2015 Online Instruction Global Online
Seven-Part Series on Pediatric Drug Development - Part 3: Regulatory Framework EU Jan 26, 2015 Online Instruction Global Online
Seven-Part Pediatric Drug Development Webinar Series - Part 4: Dosing in Children Jan 26, 2015 Online Instruction Global Online
Seven-Part Series on Pediatric Drug Development - Part 2: Regulatory Framework US Overview Jan 26, 2015 Online Instruction Global Online
Seven-Part Series on Pediatric Drug Development - Part 5: Technical Development: Pediatric Formulations Jan 26, 2015 Online Instruction Global Online
Basics of the IND Jan 26, 2015 Online Instruction Global Online
Basics of the NDA Jan 26, 2015 Online Instruction Global Online
Regulatory Aspects of Prescription Drug/Biologics Advertising and Promotional Labeling Jan 26, 2015 Online Instruction Global Online
Seven-Part Series on Pediatric Drug Development - Part 7: Operational Challenges of Pediatric Clinical Trials Jan 26, 2015 Online Instruction Global Online
Supplements and Other Changes to an Approved Application Jan 26, 2015 Online Instruction Global Online
Clinical Trials Transparency 3 Part Webinar Series - Part 3: Understanding the Legislation Landscape: Regulatory Updates from the FDA, EMA and Health Canada Jan 26, 2015 Online Instruction Global Online
Pharmacovigilance and Risk Management Strategies 2015 Jan 26, 2015 ACPE, CME, IACET, RN Meetings North America Washington, DC, United States
EudraVigilance - electronic reporting of ICSRs in the EEA Jan 28, 2015 In-Person Instruction Europe London, United Kingdom
18th Annual Workshop in Japan for Clinical Data Management Jan 29, 2015 Meetings Japan Tokyo, Japan
5th DIA Labeling Workshop in Japan Feb 03, 2015 Meetings Japan Tokyo, Japan
Regulatory Aspects of Prescription Drug/Biologics Advertising and Promotional Labeling Feb 05, 2015 IACET Online Instruction Global Online
Excellence in Pharmacovigilance: Clinical Trials and Post-Marketing Feb 09, 2015 In-Person Instruction Europe London, United Kingdom
1st Maghreb Regulatory Conference Feb 10, 2015 Meetings Europe Algiers, Algeria
Clinical Trials Transparency 3 Part Webinar Series - Part 3: Understanding the Legislation Landscape: Regulatory Updates from the FDA, EMA and Health Canada Feb 10, 2015 IACET Online Instruction Global Online
Bayesian Methods for Drug Safety Evaluation and Signal Detection Feb 10, 2015 IACET In-Person Instruction North America Arlington, VA, United States
Use of Historical Data in Clinical Trials Feb 10, 2015 IACET 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 IACET Meetings North America Arlington, VA, United States
ICH endorsed PhV training course Feb 12, 2015 In-Person Instruction Europe Algiers, Algeria
EudraVigilance - electronic reporting of ICSRs in the EEA Feb 16, 2015 In-Person Instruction Europe London, United Kingdom
OPDP/APLB and Compliance 101: A Primer Feb 17, 2015 ACPE, IACET In-Person Instruction North America Washington, DC, United States
Marketing Pharmaceuticals 2015: Drug/Device Marketing in an Evolving Environment Feb 18, 2015 ACPE, IACET Meetings North America Washington, DC, United States
eXtended EudraVigilance Medicinal Product Dictionary (XEVMPD) Feb 19, 2015 In-Person Instruction Europe London, United Kingdom
Art of Writing a Clinical Overview Feb 24, 2015 IACET Online Instruction Global Online
Introduction to Signal Detection and Data Mining Mar 02, 2015 IACET In-Person Instruction North America Washington, DC, United States
eXtended EudraVigilance Medicinal Product Dictionary (XEVMPD) Mar 02, 2015 In-Person Instruction Europe Madrid, Spain
EudraVigilance - electronic reporting of ICSRs in the EEA Mar 04, 2015 In-Person Instruction Europe Madrid, Spain
Pricing, Economic, Reimbursement, Market Share (PERMS) Strategy: An Interactive Holistic Approach in Rare Diseases Mar 05, 2015 IACET Online Instruction Global Online
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
Introduction to Pharmacovigilance and Rules for Expedited Reporting of Individual Case Safety Reports (ICSRs) in Europe Mar 10, 2015 In-Person Instruction Europe London, United Kingdom
Preparing a Clinical Trial Budget Mar 10, 2015 IACET, PMI Online Instruction Global Online
EudraVigilance - electronic reporting of ICSRs in the EEA Mar 11, 2015 In-Person Instruction Europe London, United Kingdom
3rd DIA Clinical Operation & Monitoring Workshop in Japan Mar 12, 2015 Meetings Japan Tokyo, Japan
Regulatory Affairs: The IND, NDA, and Postmarketing Mar 15, 2015 In-Person Instruction North America Irvine, CA, United States
Core Curriculum Mar 15, 2015 In-Person Instruction North America Glendale, AZ, United States
Medical Communications: Compliance in 2015 Mar 16, 2015 In-Person Instruction North America
EudraVigilance - electronic reporting of ICSRs in the EEA Mar 16, 2015 In-Person Instruction Europe Vienna, Austria
Medical & Scientific Communications 2015 Annual Forum Mar 16, 2015 Meetings North America Glendale, AZ, United States
eXtended EudraVigilance Medicinal Product Dictionary (XEVMPD) Mar 19, 2015 In-Person Instruction Europe Vienna, Austria
2nd DIA Risk Management Workshop in Japan Mar 19, 2015 Meetings Japan Tokyo, Japan
Premarketing Clinical Safety and Pharmacovigilance Mar 23, 2015 IACET In-Person Instruction North America Washington, DC, United States
Clinical Data Validation Workshop Mar 25, 2015 Meetings China
EudraVigilance - Electronic Reporting of ICSRs in the EEA Mar 25, 2015 In-Person Instruction Europe Bucharest, Romania
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
Information Day on ICH Apr 13, 2015 Meetings Europe Paris, France
8th Annual Clinical Forum Apr 13, 2015 Meetings Europe Paris, France
27th Annual EuroMeeting Apr 13, 2015 Meetings Europe Paris, France
EM01: HOT TOPICS IN PHARMACOVIGILANCE AND ADVERSE REACTION REPORTING Apr 13, 2015 In-Person Instruction Europe Paris, France
EM02: INTERACTIONS BETWEEN REGULATORY AND LEGAL IN INTELLECTUAL PROPERTY, PRODUCT LIABILITY AND COMPETITION Apr 13, 2015 In-Person Instruction Europe Paris, France
EM03: ANALYSIS OF SAFETY DATA FROM CLINICAL TRIALS Apr 13, 2015 In-Person Instruction Europe Paris, France
EM04: PRIVACY AND PERSONAL DATA PROTECTION IN DRUG DEVELOPMENT Apr 13, 2015 In-Person Instruction Europe Paris, France
EM05: MOVING FROM RISK MANAGEMENT TO BENEFIT/RISK MANAGEMENT EMBEDDING PHARMACOVIGILANCE PRINCIPLES INTO THE PRODUCT LIFE CYCLE Apr 13, 2015 In-Person Instruction Europe Paris, France
EM06: MODELLING AND SIMULATION Apr 13, 2015 In-Person Instruction Europe Paris, France
CF01: A LEGAL UPDATE: RECENT AND CURRENT DEVELOPMENTS IN EUROPEAN PHARMACEUTICAL LAW Apr 13, 2015 In-Person Instruction Europe Paris, France
CF02: ENSURING DATA QUALITY AND DETECTING POTENTIAL FRAUD/GCP MISCONDUCT Apr 13, 2015 In-Person Instruction Europe Paris, France
Regulatory Affairs for Biologics Apr 14, 2015 In-Person Instruction North America Bethesda, MD, United States
EudraVigilance - electronic reporting of ICSRs in the EEA Apr 15, 2015 In-Person Instruction Europe Paris, France
Advanced Signal Detection - Tools, Triage, Evaluation, and Escalation Apr 20, 2015 In-Person Instruction North America Washington, DC, United States
DIA/FDA Statistics 2015 Forum Apr 20, 2015 Meetings North America North Bethesda, MD, United States
EudraVigilance - electronic reporting of ICSRs in the EEA Apr 20, 2015 In-Person Instruction Europe London, United Kingdom
9th DIA Annual Conference in Japan for Asian New Drug Development Apr 20, 2015 Meetings Japan Tokyo, Japan
eXtended EudraVigilance Medicinal Product Dictionary (XEVMPD) Apr 23, 2015 In-Person Instruction Europe London, United Kingdom
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
Key Considerations for the Development and Marketing of Biosimilar Products Apr 27, 2015 In-Person Instruction North America Washington, DC, United States
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
Pragmatic Approaches to Drug Safety Across the Premarketing and Postmarketing Continuum Apr 29, 2015 ACPE, IACET In-Person Instruction North America Washington, DC, United States
EudraVigilance - electronic reporting of ICSRs in the EEA May 04, 2015 In-Person Instruction Europe San Marino, San Marino
Basics of the IND Phase May 04, 2015 IACET Online Instruction Global Online
Oversight of Clinical Monitoring: Trends and Strategies May 05, 2015 IACET Online Instruction Global Online
Introduction to Health Technology Assessment (HTA) May 06, 2015 In-Person Instruction Europe Amsterdam, Netherlands
eRegulatory and Intelligence Annual Conference May 11, 2015 Meetings North America Philadelphia, PA, United States
Electronic Submissions: The Next Era of Electronic Submissions May 14, 2015 IACET In-Person Instruction North America Philadelphia, PA, United States
Essentials of Clinical Study Management May 18, 2015 In-Person Instruction Europe London, United Kingdom
Pre-Marketing Clinical Safety May 18, 2015 In-Person Instruction Europe London, United Kingdom
Basics of the NDA Phase May 18, 2015 IACET Online Instruction Global Online
Introduction to Pharmacovigilance and Rules for Expedited Reporting of Individual Case Safety Reports (ICSRs) in Europe May 19, 2015 In-Person Instruction Europe London, United Kingdom
EudraVigilance - electronic reporting of ICSRs in the EEA May 20, 2015 In-Person Instruction Europe London, United Kingdom
The 7th DIA China Annual Meeting May 24, 2015 Meetings China Shanghai, China
How to Prepare for a Safety Inspection Jun 01, 2015 IACET Online Instruction Global Online
EudraVigilance - electronic reporting of ICSRs in the EEA Jun 03, 2015 In-Person Instruction Europe Berlin, Germany
EudraVigilance - electronic reporting of ICSRs in the EEA Jun 08, 2015 In-Person Instruction Europe London, United Kingdom
Medical Approach in Diagnosis and Management of ADRs Jun 10, 2015 In-Person Instruction Europe Charenton Le Pont, Paris, France
eXtended EudraVigilance Medicinal Product Dictionary (XEVMPD) Jun 11, 2015 In-Person Instruction Europe London, United Kingdom
Diagnosis and Management of Drug-Induced Liver Injury (DILI) Jun 11, 2015 In-Person Instruction Europe Charenton Le Pont, Paris, France
#20: The Sunshine Act: Understanding the Essentials of Compliance Jun 14, 2015 CME, IACET, RN In-Person Instruction North America Washington, DC, United States
#21: Leadership: How to Organize and Lead People in a Work Group Jun 14, 2015 IACET, PMI In-Person Instruction North America Washington, DC, United States
#22: Successful Drug Development: Best Practices for Clinical Trial Design, Agency Interactions, and Regulatory Document Writing Jun 14, 2015 IACET In-Person Instruction North America Washington, DC, United States
#23: How to Prepare for an FDA Inspection Jun 14, 2015 CME, IACET, RN In-Person Instruction North America Washington, DC, United States
#24: Pharmacogenomics and Companion Diagnostics: The Future of Clinical Trials, New Product Development and the Practice of Medicine Jun 14, 2015 ACPE, CME, IACET, RN In-Person Instruction North America Washington, DC, United States
DIA 2015 51st Annual Meeting: Develop. Innovate. Advance. Jun 14, 2015 Meetings North America Washington, DC, United States
#40: Analysis of Safety Data from Clinical Trials Jun 14, 2015 ACPE, CME, IACET, RN In-Person Instruction North America Washington, DC, United States
#41: Quality Oversight of CROs-Clinical Vendors Jun 14, 2015 IACET In-Person Instruction North America Washington, DC, United States
#42: Fundamentals of ANDA Submissions and FDA Expectations Under GDUFA Jun 14, 2015 CME, IACET, RN In-Person Instruction North America Washington, DC, United States
#43: Clinical Statistics for Nonstatisticians Jun 14, 2015 ACPE, CME, IACET, RN In-Person Instruction North America Washington, DC, United States
#44: Risk Management and Safety Communication Strategies Jun 14, 2015 ACPE, CME, IACET, RN In-Person Instruction North America Washington, DC, United States
#45: The Good Pharmacovigiliance Practices in the EU: Global Applications Jun 14, 2015 CME, IACET, RN In-Person Instruction North America Washington, DC, United States
#30: Japan Regulatory Environment: Overview of the Organization, Processes, Systems, and Changes Affecting Pharmaceutical Development Jun 14, 2015 IACET In-Person Instruction North America Washington, DC, United States
#31: Preparing for a US FDA Advisory Committee Meeting Jun 14, 2015 IACET In-Person Instruction North America Washington, DC, United States
#32: Influencing Culture, Avoiding Bureaucracy, and Encouraging Innovation Jun 14, 2015 IACET In-Person Instruction North America Washington, DC, United States
#33: Large-Scale Regulatory Functional Outsourcing: Emerging Trends, Challenges, and Decision Criteria Jun 14, 2015 IACET In-Person Instruction North America Washington, DC, United States
#34: Preparation of Risk Evaluation and Mitigation Strategies Assessment Reports Jun 14, 2015 ACPE, CME, IACET, RN In-Person Instruction North America Washington, DC, United States
#35: Ethical Issues in Clinical Trials Jun 14, 2015 CME, IACET, RN In-Person Instruction 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 ACPE, IACET In-Person Instruction North America Boston, MA, United States
Development of a Clinical Study Report Aug 10, 2015 IACET In-Person Instruction North America Boston, MA, United States
Regulatory Affairs: The IND, NDA, and Postmarketing Aug 10, 2015 In-Person Instruction North America Boston, MA, United States
Clinical Project Management Aug 24, 2015 IACET, PMI 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
Adaptive Design in Clinical Trials: When and How to Apply Sep 15, 2015 In-Person Instruction North America Washington, DC, United States
Clinical Project Management Part I Sep 16, 2015 In-Person Instruction Europe London, United Kingdom
Patient Engagement in Benefit-Risk Assessment throughout the Life Cycle of Medical Products Sep 17, 2015 Meetings North America North Bethesda, MD, United States
Paediatric Investigation Plans (PIP) Sep 17, 2015 In-Person Instruction Europe London, United Kingdom
Post-Authorisation Safety Studies (PASS) Sep 21, 2015 In-Person Instruction Europe Berlin, Germany
Medical Devices: Regulation and lifecycle management Sep 21, 2015 In-Person Instruction Europe Vienna, Austria
Quality by Design - New Concepts for Chemical and Biotech Product Development and Optimisation Sep 21, 2015 In-Person Instruction Europe Vienna, Austria
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 IACET Online Instruction Global Online
Introduction to the role of QPPVs Oct 12, 2015 In-Person Instruction Europe
9th European Forum for Qualified Person for Pharmacovigilance (QPPV) and Pre-Conference Workshop Oct 13, 2015 Meetings Europe London, United Kingdom
Practical GCP Compliance Auditing of Trials and Systems Oct 14, 2015 In-Person Instruction Europe London, United Kingdom
How to Prepare for Your Meeting with Health Authorities and Present Your Product Oct 14, 2015 In-Person Instruction Europe London, United Kingdom
Clinical Statistics for Non-Statisticians Oct 15, 2015 In-Person Instruction Europe London, United Kingdom
Risk Management and Safety Communication Oct 26, 2015 In-Person Instruction North America Washington, DC, United States
Benefit/Risk Management Nov 03, 2015 In-Person Instruction Europe Charenton Le Pont, Paris, France
Signal Management in Pharmacovigilance Nov 05, 2015 In-Person Instruction Europe Charenton Le Pont, Paris, France
Postmarketing Drug Safety & Pharmacovigilance Nov 09, 2015 ACPE, IACET 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
US Regulatory Affairs: A Comprehensive Review of Regulatory Procedures for INDs and NDAs in the US Nov 16, 2015 In-Person Instruction Europe London, United Kingdom
Clinical Project Management Part II Nov 16, 2015 In-Person Instruction Europe London, United Kingdom
Biopharmaceuticals, Biosimilars and Advanced Therapies - Development and Regulatory Framework in Europe Nov 25, 2015 In-Person Instruction Europe Vienna, Austria
Essentials of European Regulatory Affairs Nov 26, 2015 In-Person Instruction Europe Vienna, Austria