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    Name Start Date Credits Format Region Location
    Clinical Investigator: Module 2 - Conducting The Study Dec 20, 2014 ACPE, CME Online Instruction North America Online
    Clinical Investigator: Module 1 - Study Preparation and Initiation Dec 20, 2014 ACPE, CME Online Instruction North America Online
    Informed Consent Dec 20, 2014 ACPE Online Instruction North America Online
    Crisis Management Dec 20, 2014 ACPE, IACET Online Instruction North America Online
    Database Management Dec 20, 2014 ACPE, IACET Online Instruction North America Online
    Literature Evaluation Dec 20, 2014 ACPE, IACET Online Instruction North America Online
    Literature Searching Dec 20, 2014 ACPE, IACET Online Instruction North America Online
    Medical Inquiries Dec 20, 2014 ACPE, IACET Online Instruction North America Online
    Medical Writing Dec 20, 2014 IACET Online Instruction North America Online
    Product Labeling Dec 20, 2014 ACPE, IACET Online Instruction North America Online
    Regulatory Issues Dec 20, 2014 ACPE, IACET Online Instruction North America Online
    Statistics for Medical Communications Professionals Dec 20, 2014 ACPE, IACET Online Instruction North America Online
    The Use of Mobile Medical Applications as Companions Dec 20, 2014 Online Instruction Global Online
    Generic Drug Labeling Proposed Rule and Safety Updates Dec 20, 2014 Online Instruction Global Online
    Emerging Technologies to Rare Disorder Drug Development: Promises and Pitfalls Dec 20, 2014 Online Instruction Global Online
    Target Product Profile – Strategies to Optimize Drug Development, Product Labeling, and Commercialization Dec 20, 2014 Online Instruction Global Online
    The Role of the Clinical Data Manager Dec 20, 2014 Online Instruction Global Online
    Implementation of the FDASIA Patient Provisions Dec 20, 2014 Online Instruction Global Online
    Complimentary: Regulatory and Real World Evidence Challenges of Rare Diseases and Orphan Drugs Dec 20, 2014 Online Instruction Global Online
    Variations in the European Union: CMC/Quality Changes Dec 20, 2014 Online Instruction Global Online
    Proarrhythmia Dec 20, 2014 Online Instruction Global Online
    Facets of Drug-Induced Kidney Injury and Regulatory Perspective Dec 20, 2014 Online Instruction Global Online
    Impact on Drug Development of Novel Translational Safety Biomarkers for Improved Detection of Drug-Induced Acute Kidney Injury Dec 20, 2014 Online Instruction Global Online
    Pharmacovigilance and Risk Management: Patient Perspective Dec 20, 2014 Online Instruction Global Online
    Complimentary Patient-Centeredness and Engagement in Clinical Research: Opportunities for Industry Dec 20, 2014 Online Instruction Global Online
    Drug Safety Regulatory Requirements Dec 20, 2014 ACPE, IACET Online Instruction Global Online
    Premarketing Clinical Trial Safety Dec 20, 2014 ACPE, IACET Online Instruction Global Online
    Postmarketing Safety Management Dec 20, 2014 ACPE, IACET Online Instruction Global Online
    Basics of Signal Detection and Pharmacoepidemiology Dec 20, 2014 ACPE, IACET Online Instruction Global Online
    Safety Audits and Inspections Dec 20, 2014 ACPE, IACET Online Instruction Global Online
    Five-Part Series on Fundamentals of Clinical Pharmacology for Drug Development - Part 1: Fundamentals of Clinical Pharmacology: Pharmacokinetics Dec 20, 2014 Online Instruction Global Online
    Five-Part Series on Fundamentals of Clinical Pharmacology for Drug Development - Part 2: Fundamentals of Clinical Pharmacology: Pharmacodynamics Dec 20, 2014 Online Instruction Global Online
    Pharmacovigilance and Global Harmonization Updates Dec 20, 2014 Online Instruction Global Online
    Five-Part Series on Fundamentals of Clinical Pharmacology For Drug Development - Part 3: Principles of Modeling and Simulation Dec 20, 2014 Online Instruction Global Online
    Five-Part Series on Fundamentals of Clinical Pharmacology for Drug Development - Part 4: Determining the Safe First Human Dose Dec 20, 2014 Online Instruction Global Online
    Five-Part Series on Fundamentals of Clinical Pharmacology for Drug Development - Part 5: Assessment of QT Prolongation Dec 20, 2014 Online Instruction Global Online
    Designed for Success: Utilizing Protocol Quality by Design (QbD) to Plan Clinical Studies Dec 20, 2014 Online Instruction Global Online
    Negotiation and Influence Dec 20, 2014 Online Instruction Global Online
    Introduction to Drug Safety Dec 20, 2014 ACPE, IACET Online Instruction Global Online
    How to Prepare for a Safety Inspection Dec 20, 2014 Online Instruction Global Online
    Implementation and Status of Periodic Benefit-Risk Evaluation Reporting (PBRER) in Canada Dec 20, 2014 Online Instruction Global Online
    Clinical Statistics for Nonstatisticians Dec 20, 2014 Online Instruction Global Online
    Advanced Clinical Statistics for Nonstatisticians Dec 20, 2014 Online Instruction Global Online
    Development of a Clinical Study Report Dec 20, 2014 Online Instruction Global Online
    Art of Writing a Clinical Overview Dec 20, 2014 Online Instruction Global Online
    Introductory Principles and Application of Risk Management within Clinical Operations Dec 20, 2014 Online Instruction Global Online
    Seven-Part Series on Pediatric Drug Development - Part 6: Preclinical Toxicology & Safety Dec 20, 2014 Online Instruction Global Online
    Complimentary - Need to Reinvent the Clinical Trial? Innovate, Collaborate & Integrate Dec 20, 2014 Online Instruction Global Online
    Disruptive Innovation in Medical Information Dec 20, 2014 Online Instruction Global Online
    A Tour of FDA Dec 20, 2014 Online Instruction Global Online
    A Tour of Health Canada Dec 20, 2014 Online Instruction Global Online
    A Tour of Health Europe Dec 20, 2014 Online Instruction Global Online
    Aspects of Regulatory History Dec 20, 2014 Online Instruction Global Online
    Bioresearch Monitoring Program (BIMO): Introduction Dec 20, 2014 Online Instruction Global Online
    The Clinical Development Process: Investigational Product, Plan, and Data Management Dec 20, 2014 Online Instruction Global Online
    Drug Safety & Adverse Event Reporting Dec 20, 2014 Online Instruction Global Online
    Ethical Review Boards Dec 20, 2014 Online Instruction Global Online
    Ethics as the Foundation to Clinical Research Dec 20, 2014 Online Instruction Global Online
    Awareness of FDA Inspections for Pharmaceutical Manufacturers Dec 20, 2014 Online Instruction Global Online
    Biotechnology: An Overview of Compliance Considerations Dec 20, 2014 Online Instruction Global Online
    Change Control Dec 20, 2014 Online Instruction Global Online
    Clinical Trial Audits and Consequences of Non-Compliance Dec 20, 2014 Online Instruction Global Online
    Computerized Systems Inspections in the Medical Device Industry Dec 20, 2014 Online Instruction Global Online
    European Union Clinical Trials Directive Dec 20, 2014 Online Instruction Global Online
    GMP Principals of SOPs Dec 20, 2014 Online Instruction Global Online
    GMP Updates - Enforcement Changes at the New FDA Dec 20, 2014 Online Instruction Global Online
    GMPs for API Bulk Manufacturers Dec 20, 2014 Online Instruction Global Online
    Good Clinical Practices (GCPs) for New Product Investigations Dec 20, 2014 Online Instruction Global Online
    Good Laboratory Practices (GLPs) Dec 20, 2014 Online Instruction Global Online
    GxPs Dec 20, 2014 Online Instruction Global Online
    HIPAA - The Impact on Clinical Research Dec 20, 2014 Online Instruction Global Online
    Introduction to GMPs Dec 20, 2014 Online Instruction Global Online
    Investigational Product Development Dec 20, 2014 Online Instruction Global Online
    ISO 14155: Obligations of Sponsors and Monitors for Medical Device Trials Dec 20, 2014 Online Instruction Global Online
    Key Concepts of Process Validation Dec 20, 2014 Online Instruction Global Online
    Laboratory Specimens for Clinical Research Dec 20, 2014 Online Instruction Global Online
    Medical Device Safety Reporting Dec 20, 2014 Online Instruction Global Online
    Orientation to GMP Compliance Dec 20, 2014 Online Instruction Global Online
    Overview of the Clinical Research Process Dec 20, 2014 Online Instruction Global Online
    Part 11: Electronic Records and Signatures - Application Dec 20, 2014 Online Instruction Global Online
    Part 11: Electronic Records; Electronic Signatures Dec 20, 2014 Online Instruction Global Online
    Principles of Good Documentation Dec 20, 2014 Online Instruction Global Online
    Protection of Human Subjects in Clinical Trials Dec 20, 2014 Online Instruction Global Online
    Selecting and Managing Clinical Contract Research Organizations (CROs) Dec 20, 2014 Online Instruction Global Online
    Understanding Post-Approval Changes Dec 20, 2014 Online Instruction Global Online
    Computerized Systems Inspections in the Pharmaceutical Industry Dec 20, 2014 Online Instruction Global Online
    Basics of the PhRMA Code Dec 20, 2014 Online Instruction Global Online
    Basics of AdvaMed Code Dec 20, 2014 Online Instruction Global Online
    Eucomed Guidelines on Interactions with Healthcare Professionals Dec 20, 2014 Online Instruction Global Online
    Introduction to Medical Device Health Care Compliance Dec 20, 2014 Online Instruction Global Online
    Foreign Corrupt Practices Act Dec 20, 2014 Online Instruction Global Online
    Global Anti-bribery Dec 20, 2014 Online Instruction Global Online
    Variations to Marketing Authorisation in Europe Dec 20, 2014 Online Instruction Global Online
    Registration of Monoclonal Antibodies Dec 20, 2014 Online Instruction Global Online
    How to Gain Approval to Market a Generic Medicinal Product in the USA Dec 20, 2014 Online Instruction Global Online
    Pharmacokinetics and Pharmacodynamics in Drug Registration Dec 20, 2014 Online Instruction Global Online
    Complimentary Quintiles/DIA Webinar - Giving Your Study The Right Start Toward Success Through Optimal Country and Site Selection Dec 20, 2014 Online Instruction Global Online
    Implementing Risk-Based Monitoring: Practical Approaches Dec 20, 2014 Online Instruction Global Online
    Complimentary - Innovative Strategies for Developing Safer Cancer Therapies Dec 20, 2014 Online Instruction Global Online
    Complimentary - Risk-Based Monitoring: Regulatory Expectation and Operational Application Dec 20, 2014 Online Instruction Global Online
    Fundamentals of Project Management for Nonproject Managers Dec 20, 2014 Online Instruction Global Online
    Planning and Managing Your Projects Dec 20, 2014 Online Instruction Global Online
    Preparing a Clinical Trial Budget Dec 20, 2014 Online Instruction Global Online
    Team Building and Development Dec 20, 2014 Online Instruction Global Online
    Introduction to the European Union Institutions and Regulatory Authority Dec 20, 2014 Online Instruction Global Online
    Introduction to US Institutions and Regulatory Authority (FDA) Dec 20, 2014 Online Instruction Global Online
    Introduction to Japanese Institutions and Regulatory Authorities Dec 20, 2014 Online Instruction Global Online
    Overview of the CTD and eCTD Dec 20, 2014 Online Instruction Global Online
    Introduction to the International Conference on Harmonisation (ICH) Dec 20, 2014 Online Instruction Global Online
    The Regulatory Development of a Drug Dec 20, 2014 Online Instruction Global Online
    Basics of Clinical Trials Dec 20, 2014 Online Instruction Global Online
    How to Register Medicinal Products through the Centralized Procedure Dec 20, 2014 Online Instruction Global Online
    How to Register Medicinal Products through the Mutual Recognition Procedure Dec 20, 2014 Online Instruction Global Online
    How to Maintain Marketing Approvals in Europe for Centrally Authorised Products Dec 20, 2014 Online Instruction Global Online
    How to Register a New Drug in the USA Dec 20, 2014 Online Instruction Global Online
    How to Register Medicinal Products through the Decentralized Procedure Dec 20, 2014 Online Instruction Global Online
    Access to Unapproved Drugs through Compassionate Use Dec 20, 2014 Online Instruction Global Online
    Regulatory Requirements for the Conduct of Clinical Trials in Europe Dec 20, 2014 Online Instruction Global Online
    Orphan Drugs in the USA, European Union, and Japan Dec 20, 2014 Online Instruction Global Online
    Regulatory Requirements for the Submission of Investigational New Drug Applications in the USA (INDs) Dec 20, 2014 Online Instruction Global Online
    Meeting Opportunities with Regulatory Agencies Dec 20, 2014 Online Instruction Global Online
    How New Electronic Trial Master File (eTMF) Data Standards Can Enhance Clinical Trial Efficiency and Quality Dec 20, 2014 Online Instruction Global Online
    Complimentary - Regulatory Solutions in the Cloud - 10 Questions You Can't Afford NOT to Ask Dec 20, 2014 Online Instruction Global Online
    Clinical Trials Transparency 3-Part Series: Moving the Debate Forward - Realizing the Benefits of Providing Greater Access to Clinical Trial Data: Part 1 - Paving the Way for Greater Access To Data Dec 20, 2014 Online Instruction Global Online
    Clinical Trials Transparency 3-Part Series: Moving the Debate Forward-Realizing the Benefits of Providing Greater Access to Clinical Trial Data: Part 2-Connecting the Research Community: Data Sharing–Perspectives from Academia and Patient Advocacy Groups Dec 20, 2014 Online Instruction Global Online
    Complimentary - From the Clinic to the CFO: Adaptive Trials and Financial Decision-Making Dec 20, 2014 Online Instruction Global Online
    Adverse Event Reporting Requirements: IND and Postmarketing Dec 20, 2014 Online Instruction Global Online
    Complimentary - The Affiliate Challenge – How to Improve Compliance and Efficiency when Working with Regional Affiliates Dec 20, 2014 Online Instruction Global Online
    The Future of Personalized Medicine and Companion Diagnostics Dec 20, 2014 Online Instruction Global Online
    Seven-Part Series on Pediatric Drug Development - Part 1: Overall Challenge: The Vision of Better Medicines for Children Dec 20, 2014 Online Instruction Global Online
    Seven-Part Series on Pediatric Drug Development - Part 3: Regulatory Framework EU Dec 20, 2014 Online Instruction Global Online
    Seven-Part Pediatric Drug Development Webinar Series - Part 4: Dosing in Children Dec 20, 2014 Online Instruction Global Online
    Seven-Part Series on Pediatric Drug Development - Part 2: Regulatory Framework US Overview Dec 20, 2014 Online Instruction Global Online
    Seven-Part Series on Pediatric Drug Development - Part 5: Technical Development: Pediatric Formulations Dec 20, 2014 Online Instruction Global Online
    Basics of the IND Dec 20, 2014 Online Instruction Global Online
    Basics of the NDA Dec 20, 2014 Online Instruction Global Online
    Regulatory Aspects of Prescription Drug/Biologics Advertising and Promotional Labeling Dec 20, 2014 Online Instruction Global Online
    Seven-Part Series on Pediatric Drug Development - Part 7: Operational Challenges of Pediatric Clinical Trials Dec 20, 2014 Online Instruction Global Online
    Supplements and Other Changes to an Approved Application Dec 20, 2014 Online Instruction Global Online
    Introduction to Pharmacoepidemiology and Applications in Premarketing and Postmarketing Surveillance, Risk Management and Value Demonstration Jan 25, 2015 IACET, RN In-Person Instruction North America Washington, DC, United States
    Pharmacovigilance and Risk Management Planning Jan 25, 2015 ACPE, IACET, RN In-Person Instruction North America Washington, DC, United States
    PBRERs Jan 25, 2015 IACET, RN In-Person Instruction North America Washington, DC, United States
    Pharmacovigilance System Master File Jan 25, 2015 IACET, RN In-Person Instruction North America Washington, DC, United States
    Pharmacovigilance and Risk Management Strategies 2015 Jan 26, 2015 ACPE, CME, IACET, RN Meetings North America Washington, DC, United States
    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
    Bayesian Methods for Drug Safety Evaluation and Signal Detection Feb 10, 2015 In-Person Instruction North America Arlington, VA, United States
    Use of Historical Data in Clinical Trials Feb 10, 2015 In-Person Instruction North America Arlington, VA, United States
    Joint Adaptive Design and Bayesian Statistics Conference: Drivers of Efficiency in Modern Medical Product Development Feb 11, 2015 Meetings North America Arlington, VA, United States
    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 In-Person Instruction North America Washington, DC, United States
    Marketing Pharmaceuticals 2015: Drug/Device Marketing in an Evolving Environment Feb 18, 2015 Meetings North America Washington, DC, United States
    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 In-Person Instruction 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
    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 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
    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
    2nd DIA Risk Management Workshop in Japan Mar 19, 2015 Meetings Japan Tokyo, Japan
    Premarketing Clinical Safety and Pharmacovigilance Mar 23, 2015 In-Person Instruction North America Washington, DC, United States
    Preparing for a FDA Advisory Committee Meeting Mar 30, 2015 IACET In-Person Instruction North America Washington, DC, United States
    CMC Workshop 2015 Apr 13, 2015 Meetings North America Bethesda, MD, United States
    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
    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
    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
    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
    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 Online Instruction Global Online
    Oversight of Clinical Monitoring: Trends and Strategies May 05, 2015 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
    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 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
    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 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
    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
    Adverse Event Reporting Requirements: IND and Post-marketing Jul 13, 2015 Online Instruction Global Online
    Interactions with the FDA during IND/NDA Phases Jul 16, 2015 Online Instruction Global Online
    Pragmatic Approaches to Drug Safety Across the Premarketing and Postmarketing Continuum Aug 10, 2015 In-Person Instruction North America
    Development of a Clinical Study Report Aug 10, 2015 IACET In-Person Instruction North America
    Regulatory Affairs: The IND, NDA, and Postmarketing Aug 10, 2015 In-Person Instruction North America
    Clinical Project Management Aug 24, 2015 In-Person Instruction North America Washington, DC, United States
    New Drug Product Development and Life Cycle Management Aug 26, 2015 In-Person Instruction North America Washington, DC, United States
    Overview of Drug Development in Japan Sep 02, 2015 Online Instruction Global Online
    DIA/FDA Oligonucleotide-based Therapeutic Conference 2015 Sep 09, 2015 Meetings North America Washington, DC, United States
    Clinical Project Management Part I Sep 16, 2015 In-Person Instruction Europe London, United Kingdom
    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 Online Instruction Global Online
    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 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