Events Calendar
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Events By Name
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Upcoming Events
- February 10 - 12, 2010 - QA/QC Strategy for Biopharmaceuticals and Biologics
- February 10, 2010 - A GMP Approach to the Detection, Correction and Prevention of Human Errors
- February 10, 2010 - Calibration Free Supersaturation Assessment And Control For The Development And Optimization Of Crystallization Processes
- February 10, 2010 - Calibration Free Supersaturation Assessment And Control For The Development And Optimization Of Crystallization Processes
- February 11, 2010 - Practical Applications of the ICH, OECD and other relevant regulatory guidance's in Drug Development
Events By Month
Click on a month below to view its associated events.
February 2010 [+] (63 total)
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Introduction to Effective Medical Writing
February 1 - 2, 2010
Malvern PA UNITED STATES
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Biopharma Freeze-Drying Course
February 1 - 3, 2010
Clearwater FL UNITED STATES
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Pharma Market Research Conference
February 1 - 2, 2010
Parsippany NJ UNITED STATES
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Basic Pharmacology Training Course
February 1 - 2, 2010
Arlington VA UNITED STATES
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2nd International Conference on Drug Discovery & Therapy
February 1 - 4, 2010
Dubai UNITED ARAB EMIRATES
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Measurement Uncertainty and Minimum Weight
February 2, 2010
UNITED STATES
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Change Control Management for a Stability Program – Potential Changes and Minimizing the Impact of Registration
February 2, 2010
Live Webinar PQ CANADA
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Fundamental Tools in Statistics for GMP Compliance
February 2 - 3, 2010
Jersey City NJ UNITED STATES
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The Drug Development Process - From Discovery to Commercialization
February 3 - 5, 2010
Malvern PA UNITED STATES
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Effective Document Management for the Pharmaceutical, Biotech & Medical Device Industries
February 3 - 4, 2010
Malvern PA UNITED STATES
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Molecular Medicine Tri-Conference
February 3 - 5, 2010
San Francisco CA UNITED STATES
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Routine Testing of Weighing Systems
February 3, 2010
UNITED STATES
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Optimization And Scale-Up Of A Hydrodynamically Limited Anti-Solvent Crystallization Process: From Lab To Plant
February 3, 2010
UNITED STATES
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Online Webinar on 21 CFR Part 11: Auditing for Part 11 Compliance
February 4, 2010
Online Training USA CA UNITED STATES
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Bay Area Pharma & Life Sciences IP Summit
February 4, 2010
San Mateo CA UNITED STATES
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The Challenges of Monitoring Impurities in Pharmaceutical Products – The Requirements in Q3 A/B and Key Factors in Setting Impurity Specifications
February 4, 2010
Live Webinar PQ CANADA
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Good Clinical Practices (GCP)
February 8 - 10, 2010
Malvern PA UNITED STATES
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Analytical Method Validation for Biologics, Biopharmaceuticals and Other Therapeutic Products
February 8 - 9, 2010
Malvern PA UNITED STATES
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FDA Inspections of Clinical Data Systems
February 8 - 9, 2010
Malvern PA UNITED STATES
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Practical Methods for Project Management
February 8 - 9, 2010
Costa Mesa CA UNITED STATES
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Statistics 101: Principles in Drug Development
February 8 - 9, 2010
Arlington VA UNITED STATES
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mplementation of the New USP and - The Basis for USP Microbiological General Chapter Testing
February 9, 2010
Live Webinar PQ CANADA
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Rheology Academy
February 9 - 11, 2010
Ashland VA UNITED STATES
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Calibration Free Supersaturation Assessment And Control For The Development And Optimization Of Crystallization Processes
February 10, 2010
UNITED STATES
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A GMP Approach to the Detection, Correction and Prevention of Human Errors
February 10, 2010
Live Webinar PQ CANADA
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QA/QC Strategy for Biopharmaceuticals and Biologics
February 10 - 12, 2010
Malvern PA UNITED STATES
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Calibration Free Supersaturation Assessment And Control For The Development And Optimization Of Crystallization Processes
February 10, 2010
UNITED STATES
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Adverse Drug Events - Reporting & Regulatory Requirements
February 11 - 12, 2010
Malvern PA UNITED STATES
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The WHO/ASEAN Stability Guidance – Recent Developments, Applying for Market Authorization and the Review of a Model Stability Study
February 11, 2010
Live Webinar PQ CANADA
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Practical Applications of the ICH, OECD and other relevant regulatory guidance's in Drug Development
February 11, 2010
Palo Alto CA UNITED STATES
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Practical Applications of the ICH, OECD and other relevant regulatory guidance's in Drug Development
February 11, 2010
Palo Alto CA UNITED STATES
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The Batch Record Review Process and Investigation of Discrepancies: Compliance, Training and Management
February 12 - 26, 2010
Live Webinar PQ CANADA
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Clinical Trial auditing - Identifying risks and building a more compliant and successful trial
February 16, 2010
Palo Alto CA UNITED STATES
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Introduction to GLP/GMP Training – An Introduction to Meeting the Requirements of 21 CFR Part 58 and 21 CFR Part 210/211;Exploring Good FDA Expectatns
February 16, 2010
Live Webinar PQ CANADA
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Clinical Trial auditing - Identifying risks and building a more compliant and successful trial
February 16, 2010
Palo Alto CA UNITED STATES
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Drug Master Files (DMFs) - Understanding & Meeting Your Global Regulatory and Processing Responsibilities
February 16, 2010
Live Webinar PQ CANADA
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A Risk-Based Approach to Environmental Monitoring – A Review of Warning Letters, Risk Analysis and Industry Best Practices for Data Collection, Monito
February 17, 2010
Live Webinar PQ CANADA
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Determination of Microbiological Rapid Method Requirements – Is There A Place for Them in Your Facilities?
February 18, 2010
Live Webinar PQ CANADA
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Effective Laboratory Safety Management
February 18 - 19, 2010
Costa Mesa CA UNITED STATES
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Conversion Prediction Of An Enzymatic Esterification With The ReactIR™ 45m And iC Quant™
February 18, 2010
UNITED STATES
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Stability testing of pharmaceuticals
February 22 - 24, 2010
Cambridge UNITED KINGDOM
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Current Expectations in the Characterization & Comparability of Product Reference Standards for Biotechnology Products
February 22, 2010
Live Webinar PQ CANADA
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Writing Effective Standard Operating Procedures and Other Process Documents
February 22 - 23, 2010
Malvern PA UNITED STATES
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FDA Inspections - What to Expect and How to Prepare
February 22 - 23, 2010
Malvern PA UNITED STATES
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Cost Contained Regulatory Compliance for the Drug, Biologics and Medical Device Industries
February 22 - 23, 2010
Malvern PA UNITED STATES
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Medical Devices: Demystifying Regulation and Guidance
February 22, 2010
Arlington VA UNITED STATES
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8th Cold Chain Management & Temperature Control Summit
February 23 - 25, 2010
Toronto ON CANADA
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Are Your Medicines Safe?
February 23, 2010
Brussels BELGIUM
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USP – Chapter 467 & GMP Requirements for Testing Residual Solvents
February 23, 2010
Live Webinar PQ CANADA
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Stability Studies for Biologics and Therapeutics: A Regulatory Perspective on Requirements, Equipment, Supporting Systems and Forced Degradation
February 24, 2010
Live Webinar PQ CANADA
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Comprehensive Overview of FDA Regulatory Compliance for Drugs and Biotech Products
February 24 - 25, 2010
Malvern PA UNITED STATES
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Writing in the Regulated Environment when English is Your Second Language
February 24 - 25, 2010
Malvern PA UNITED STATES
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Marketing, Advertising and Promotion of Pharmaceuticals and Medical Devices
February 24 - 25, 2010
Malvern PA UNITED STATES
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Solid Dosage Production in cGMP Manufacturing
February 24 - 25, 2010
Montreal PQ CANADA
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Containment Technology Forum: Basics and Beyond (E06)
February 24 - 25, 2010
Tampa FL UNITED STATES
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5th Annual Biomarkers Congress
February 25 - 26, 2010
Manchester AL UNITED KINGDOM
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The Role of Investigative Toxicology and Safety Biomarkers in Drug Safety Evaluations
February 25, 2010
Palo Alto CA UNITED STATES
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Refresher Training Course on GMP regulations and guidelines
February 25 - 26, 2010
Montreal ON CANADA
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Pharmacon Conference: Medicines Counterfeiting
February 25, 2010
Belgrade SERBIA AND MONTENEGRO
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The Role of Investigative Toxicology and Safety Biomarkers in Drug Safety Evaluations
February 25, 2010
Palo Alto CA UNITED STATES
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Medical Devices: EU Directives, Guidance, CE Marking and ISO Standard Certifications
February 25, 2010
Live Webinar PQ CANADA
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FDA’s New Guidance “Current Good Manufacturing Requirements for Combination Products” – cGMP Requirements
February 25, 2010
Live Webinar PQ CANADA
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Pittcon Conference and Expo 2010
February 28, 2010 - March 5, 2010
Orlando FL UNITED STATES
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March 2010 [+] (66 total)
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Biopharma Freeze-Drying Course
March 1 - 3, 2010
Amsterdam NETHERLANDS
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Pediatric Clinical Trial
March 1 - 2, 2010
Arlington VA UNITED STATES
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Adverse Drug Events - Reporting & Regulatory Requirements
March 1 - 2, 2010
Berlin GERMANY
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Good Clinical Practice for Medical Device Investigations
March 1 - 2, 2010
Malvern PA UNITED STATES
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Biostatistics for Non-Statisticians
March 1 - 3, 2010
Berlin GERMANY
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Online Training Webinar for Compliance & Regulatory Professional
March 2, 2010
Online DE UNITED STATES
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Corporate Compliance Training on the Topic of Business, Project and Compliance Risk
March 2, 2010
Online DE UNITED STATES
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Stability Programs for Product Shelf Life - From Development to Approval
March 2 - 3, 2010
Malvern PA UNITED STATES
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Good Clinical Practice Auditing
March 3 - 4, 2010
Malvern PA UNITED STATES
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The Drug Development Process - From Discovery to Commercialization
March 3 - 5, 2010
Berlin GERMANY
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Regulatory Corporate Compliance Training on FDA Inspections: What to Expect and How to Prepare
March 3, 2010
Online DE UNITED STATES
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Quality by Design for analytical methods: a revolution in method lifecycle management?
March 4, 2010
London UNITED KINGDOM
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Preparing and Closing Microbial Investigations – A Review of Industry Practices, Common Mistakes, Risk Analysis and Strategies
March 4, 2010
Live Webinar PQ CANADA
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Introduction to Molecular Biology Techniques
March 8 - 10, 2010
Malvern PA UNITED STATES
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Good Clinical Practices (GCP)
March 8 - 10, 2010
Berlin GERMANY
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Preparation of FDA Submissions (INDs, NDAs, BLAs, ANDAs, Post-Approval Supplements) and Communicating with the FDA
March 8 - 9, 2010
Malvern PA UNITED STATES
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Summit for Clinical Trials Operations Executives (SCOPE)
March 8 - 11, 2010
Philadelphia PA UNITED STATES
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The EU Clinical Trial Directive
March 9 - 10, 2010
Malvern PA UNITED STATES
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How to Prepare for a Systems-based Inspection - Understanding FDA's Risk-Based Inspections Approach
March 9 - 10, 2010
Malvern PA UNITED STATES
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GMP Annual Training –Exploring Good Manufacturing Practices Updates and FDA Regulatory Expectations
March 9 - 18, 2010
Live Webinar PQ CANADA
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The CTD/eCTD: Building the Marketing Application throughout Clinical Development
March 10 - 12, 2010
Malvern PA UNITED STATES
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Financial Fundamentals for Non-Financial Personnel - How Financial Issues Impact Business
March 11 - 12, 2010
Malvern PA UNITED STATES
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How to Develop an Effective Complaint Handling, and Post Market Surveillance Program for Drugs and Devices
March 11 - 12, 2010
Malvern PA UNITED STATES
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European Filing & Registration Procedures
March 11 - 12, 2010
Malvern PA UNITED STATES
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Comprehensive Forced Degradation Studies to Validate Stability–Indicating Methods for Biotechnology Products
March 15, 2010
Live Webinar PQ CANADA
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Latin America – Understanding the Structure, Regulatory Requirements and Compliance Processes for the Pharmaceutical, Biotech and Medical Device Indus
March 15 - 22, 2010
Live Webinar PQ CANADA
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Preparing the CMC Section for NDAs/CTDs/INDs
March 15 - 16, 2010
Costa Mesa CA UNITED STATES
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Cleanroom Microbiology for the Non-Microbiologist
March 15 - 16, 2010
Malvern PA UNITED STATES
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Labeling and Labeling Controls for Medical Devices
March 15 - 16, 2010
Malvern PA UNITED STATES
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Clinical Trials Design for Medical Devices
March 15 - 16, 2010
Malvern PA UNITED STATES
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Validation of Computer Systems
March 15 - 16, 2010
Berlin GERMANY
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XGen Congress
March 15 - 19, 2010
San Diego CA UNITED STATES
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Basic Drug Development: From Molecule to Market
March 15 - 16, 2010
Arlington VA UNITED STATES
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Pharma R&D Partnering World Asia 2010
March 16 - 19, 2010
Singapore SINGAPORE
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Drug Discovery Technology World Asia 2010
March 16 - 19, 2010
Singapore SINGAPORE
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World Pharma Trials Asia 2010
March 16 - 19, 2010
Singapore SINGAPORE
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Biologic Manufacturing World Asia 2010
March 16 - 19, 2010
Singapore SINGAPORE
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Pharma & Biotech Supply Chain Management World Asia
March 16 - 19, 2010
Singapore SINGAPORE
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BioPharma Asia Convention 2010
March 16 - 19, 2010
Singapore SINGAPORE
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Microbiology of Water in a GMP Environment
March 16, 2010
Live Webinar PQ CANADA
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Preparing for FDA GLP Audits
March 17, 2010
Live Webinar PQ CANADA
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Technical Writing for Pharmaceutical, Medical Device and Biotech Industries
March 17 - 19, 2010
Malvern PA UNITED STATES
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Sterilization Procedures: Technology, Equipment & Validation
March 17 - 18, 2010
Malvern PA UNITED STATES
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Purchasing Controls in the Medical Device Industry
March 17 - 18, 2010
Malvern PA UNITED STATES
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Developing an Environmental Plan for a Controlled/Classified Environment
March 18, 2010
Live Webinar PQ CANADA
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Overview of FDA Regulatory Compliance for Medical Devices
March 22 - 23, 2010
Dublin IRELAND
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Project Management for Phase 1 & 2 Clinical Trials
March 22 - 23, 2010
Malvern PA UNITED STATES
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Aseptic Processing in the Manufacture of Biotech and Pharmaceutical Products
March 22 - 23, 2010
Costa Mesa CA UNITED STATES
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Pharmaceutical Production Batch Record Review
March 22 - 23, 2010
Costa Mesa CA UNITED STATES
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Asthma and COPD: Clinical Drug Development
March 22 - 23, 2010
Arlington VA UNITED STATES
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microRNA in Human Disease & Development
March 22 - 24, 2010
Cambridge MA UNITED STATES
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6th Annual Stability Testing Conference
March 23 - 24, 2010
Somerset NJ UNITED STATES
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Future directions for pharmacy education
March 24, 2010
Reading UNITED KINGDOM
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Root Cause Analysis for CAPA
March 24 - 26, 2010
Dublin IRELAND
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Optimization of Drug-Like Properties in Drug Discovery - Assessment and Structure Modification Strategies
March 24 - 26, 2010
Costa Mesa CA UNITED STATES
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Project Management for Phast 3 & LCM (Life Cycle Management) of the Drug Development Process
March 24 - 25, 2010
Malvern PA UNITED STATES
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Investigating Out-of-Specification (OOS) Test Results for Pharmaceutical Production
March 24, 2010
Live Webinar PQ CANADA
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Cancer Stem Cells
March 24 - 25, 2010
Cambridge MA UNITED STATES
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Effective Quality Assurance Auditing for FDA Regulated Industries
March 29 - 30, 2010
Dublin IRELAND
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Selecting and Managing CROs
March 29 - 30, 2010
Malvern PA UNITED STATES
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Gobal REgulatory Affairs: An Overview of Drugs and Biologics
March 29 - 30, 2010
Arlington VA UNITED STATES
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4th Improving Solubility
March 29 - 31, 2010
Philadelphia PA UNITED STATES
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Refresher Training Course on GMP regulations and guidelines
March 30 - 31, 2010
Vancouver BC CANADA
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Leadership Workshop
March 30 - 31, 2010
Montreal PQ CANADA
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Leadership Workshop
March 30 - 31, 2010
Montreal PQ CANADA
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Drug Master Files (DMFs) - Understanding and Meeting Your Regulatory and Process Responsibilities
March 31, 2010 - April 1, 2010
Malvern PA UNITED STATES
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April 2010 [+] (10 total)
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Collaborations, Deals and Alliances Congress
April 11 - 14, 2010
Philadelphia PA UNITED STATES
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Prescription Drug Labeling Regulation
April 12 - 13, 2010
Arlington VA UNITED STATES
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FIP Quality International 2010 Managing quality across the drug supply chain: from product inception to patient utilization
April 15 - 16, 2010
London UNITED KINGDOM
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Logichem 2010
April 20 - 22, 2010
London MN UNITED KINGDOM
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Cancer: Pathophysiology, Current Therapies, Clinical Trials and Drug Development
April 26 - 28, 2010
Washington DC UNITED STATES
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Clinical Trial Planning and Management
April 26 - 27, 2010
Arlington VA UNITED STATES
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LogiPharma Europe 2010
April 27 - 29, 2010
Geneva AL SWITZERLAND
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Successful eCTD Lifecycle Management
April 27 - 28, 2010
London UNITED KINGDOM
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Rheology Academy
April 27 - 29, 2010
Ashland VA UNITED STATES
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Reaction Progress Kinetic Analysis: A Powerful Methodology For Streamlining The Study Of Complex Organic Reactions
April 28, 2010
UNITED STATES
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May 2010 [+] (11 total)
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BIO International Convention 2010
May 3 - 6, 2010
Chicago IL UNITED STATES
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Global Pharmacovigilance Training Course
May 3 - 5, 2010
Arlington VA UNITED STATES
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Drug Development Decisions: The NDA Simulation Workshop
May 3 - 5, 2010
Arlington VA UNITED STATES
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Pharmacokinetic Concepts in Drug Development
May 10 - 12, 2010
Arlington VA UNITED STATES
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Faster, Better Organic Chemistry Through The Use Of Real-Time In Situ FTIR Technology & Software Optimized For The Organic Chemist
May 12, 2010
UNITED STATES
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The twelth advanced level workshop on Pharmacokinetic - Pharmacodynamic data analysis: A hands-on residential course using WinNonlin
May 16 - 20, 2010
Cambridge UNITED KINGDOM
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Pharmaceutical License Meeting
May 17 - 18, 2010
Madrid SPAIN
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Global Clinical Outsourcing Forum
May 18 - 19, 2010
Munich GERMANY
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New Clinical Statisticians Training Course
May 24 - 25, 2010
Arlington VA UNITED STATES
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5th Annual Pharmaceutical & Biotech Patent Litigation Strategies
May 24 - 26, 2010
London UNITED KINGDOM
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Interphex at Total Processing & Packaging 2010
May 25 - 27, 2010
Birmingham UNITED KINGDOM
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June 2010 [+] (5 total)
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DDI-2010: 13th International Conference on Drug-Drug Interactions
June 14 - 16, 2010
Seattle WA UNITED STATES
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The 9th Annual Biological Production Forum 2010
June 21 - 23, 2010
Frankfurt GERMANY
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Oncologic Development Strategies: Protocol Development and Biomarker Applications
June 21 - 23, 2010
Arlington VA UNITED STATES
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Immunogenicity, Prediction, Detection and Effective Assay Development
June 21 - 23, 2010
Munich GERMANY
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Biologics Drug Development: Manufacturing, Non-Clinical, and Regulatory Requirements
June 28 - 30, 2010
Arlingon VA UNITED STATES
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July 2010 [+] (3 total)
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Drug Development for Pharmaceutical Physicians and Scientists Part I
July 12 - 13, 2010
Arlington VA UNITED STATES
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Cancer 202: A Basic Overview of Current Therapies for New Oncology Researchers
July 19 - 20, 2010
Arlington VA UNITED STATES
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Eleventh Annual Land O’Lakes Bioanalytical Conference
July 19 - 23, 2010
Merrimac WI UNITED STATES
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August 2010 [+] (2 total)
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Rheology Academy
August 10 - 12, 2010
Ashland VA UNITED STATES
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Medifest South Africa
August 24 - 26, 2010
Cape Town SOUTH AFRICA
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September 2010 [+] (4 total)
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The RPS conference 2010: Supporting patient and professional decision making
September 5 - 6, 2010
London UNITED KINGDOM
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Thirteenth Annual Land O’Lakes Conference on Drug Metabolism/Applied Pharmacokinetics
September 13 - 17, 2010
Merrimac WI UNITED STATES
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The Pan African Health Expo and Conference 2010
September 16 - 18, 2010
Johannesburg AL SOUTH AFRICA
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3rd International Symposium on Green Processing in the Pharmaceutical & Fine Chemical Industries
September 30, 2010 - October 1, 2010
Boston MA UNITED STATES
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October 2010 [+] (0 total)
November 2010 [+] (1 total)
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Rheology Academy
November 9 - 11, 2010
Ashland VA UNITED STATES
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December 2010 [+] (1 total)
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Medifest India
December 10 - 12, 2010
New Delhi INDIA
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January 2011 [+] (0 total)
February 2011 [+] (0 total)
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