Events Calendar
Upcoming Events
- May 24, 2013 - Food and Dietary Supplement Goods Manufacturing Practices
- May 27 - 28, 2013 - Pharmaceutical Networking Meeting PharmaVenue
- May 30, 2013 - Princeton Supply Chain Workshop
- May 30 - 31, 2013 - Comprehensive Overview of FDA Regulatory Compliance for Medical Devices
- June 3 - 4, 2013 - Comprehensive Overview of FDA Regulatory Compliance for Drug and Biotech Products
Events By Month
Click on a month below to view its associated events.
May 2013 [+] (28 total)
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10th Annual Strategic Alliance Management Congress
May 6 - 8, 2013
Philadelphia PA US
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Life Sciences Transportation Seminar
May 7, 2013
New Brunswick NJ US
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The Sunshine Act Reporting for Clinical Trials
May 7, 2013
California CA US
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The Infamous Form FDA 483: How you respond can make or break you
May 9, 2013
san francisco CA US
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Effective Document Management for the Pharmaceutical, Biotech and Medical Device Industries
May 9 - 10, 2013
King of Prussia PA US
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Pediatric Clinical Trial Design
May 13 - 14, 2013
Berlin DE
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Generics and Patent Strategies
May 13 - 14, 2013
London UK
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2013 PDA Container Closure Components and Systems Workshop
May 14 - 15, 2013
Bethesda MD US
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Establish and Maintain an Effective Supplier Qualification Program
May 14, 2013
san francisco CA US
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Freeze Drying: 2-Day Product and Process Course
May 14 - 15, 2013
Winchester
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2013 PDA/FDA Glass Packaging Conference
May 15 - 16, 2013
Bethesda MD US
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Life Sciences Transportation Seminar
May 16, 2013
Cambridge MA US
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FDA guidance “The Quality Systems Approach To the Pharmaceutical Good Manufacturing Practices"
May 16, 2013
Online Event CA
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"Diabetes & Complications" Symposiums and Grand Rounds
May 17 - 19, 2013
Kuala Lumpur MY
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The fifteenth advanced level workshop on PK/PD data analysis
May 19 - 23, 2013
Cambridge UK
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2013 PDA/FDA Process Validation Workshop
May 20 - 21, 2013
Bethesda MD US
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ADC Summit 2013
May 20 - 21, 2013
London UK
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The Hitchhiker’s guide to 483s and Warning Letters
May 21, 2013
Online Event ON CA
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Life Sciences Transportation Seminar
May 21, 2013
Research Triangle Park NC US
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Writing and Enforcing Effective SOPs
May 21, 2013
san francisco CA US
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Translational CNS Summit
May 21 - 23, 2013
Boston MA US
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Respiratory Drug Delivery (RDD) Europe 2013
May 21 - 24, 2013
Berlin DE
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Medical Foods: Practical Tips to Meet FDA Requirements for Claims and Quality
May 22, 2013
san francisco CA US
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7th annual Clinical Trial Logistics
May 22 - 23, 2013
London UK
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Food and Dietary Supplement Goods Manufacturing Practices
May 24, 2013
Palo Alto CA US
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Pharmaceutical Networking Meeting PharmaVenue
May 27 - 28, 2013
Madrid ES
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Comprehensive Overview of FDA Regulatory Compliance for Medical Devices
May 30 - 31, 2013
Berlin DE
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Princeton Supply Chain Workshop
May 30, 2013
Princeton NJ US
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June 2013 [+] (27 total)
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Comprehensive Overview of FDA Regulatory Compliance for Drug and Biotech Products
June 3 - 4, 2013
Los Angeles CA US
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Radiation Safety Officer Training for Laboratory Professionals
June 3 - 7, 2013
Boston MA US
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Exploratory Clinical Development World Europe 2013
June 4 - 6, 2013
London UK
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Pharma Outsourcing & Procurement Summit 2013
June 5 - 6, 2013
Berlin DE
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OrthoTec Conference 2013
June 5 - 6, 2013
Winona Lake IN US
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Importing and Exporting Medical Devices: A Primer on Regulatory Strategy and Requirements
June 6, 2013
san francisco CA US
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Freeze Drying: 2-Day Product and Process Course
June 9 - 10, 2013
Winchester
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Good Manufacturing Practices
June 10 - 12, 2013
Los Angeles CA US
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42nd Society of Pharmaceutical and Biotech Trainers (SPBT) Annual Conference
June 10 - 13, 2013
Orlando FL US
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2013 PDA/FDA Pharmaceutical Supply Chain Workshop
June 10 - 12, 2013
Bethesda MD US
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Redefining the "C" in CGMP Conference
June 11 - 13, 2013
Baltimore MD US
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Trial Master File (TMF): FDA Expectations from Sponsors and Sites
June 11, 2013
san francisco CA US
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Baltimore Classroom Training
June 11 - 12, 2013
Baltimore MD US
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MD&M East Conference & Expo
June 17 - 20, 2013
Philadelphia PA US
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MD&M East Conference & Expo
June 17 - 20, 2013
Philadelphia PA US
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2nd International Conference and Exhibition on Neurology and Therapeutics
June 17 - 19, 2013
chicago IL US
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ICH Q10 Pharmaceutical Quality System
June 18, 2013
Online Event CA
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Dissolution testing for the pharmaceutical industry
June 19 - 21, 2013
London UK
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2013 PDA Aseptic-Sterilization Conference
June 20 - 21, 2013
Chicago IL US
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ADMET Drug Properties in Drug Discovery and Development
June 20 - 21, 2013
Barcelona ES
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Biobanking
June 24 - 25, 2013
London UK
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John Collins
June 24 - 25, 2013
London UK
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Preparation of FDA Submissions (INDs, NDAs, BLAs, ANDAs, Post-Approval Supplements) and Communicating with the FDA
June 24 - 25, 2013
Los Angeles CA US
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Preparing the CMC Section for NDAs-CTDs-INDs
June 24 - 25, 2013
King of Prussia PA US
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Clinical Analytics for Decision Support
June 25 - 27, 2013
Boston MA US
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Natasha
June 26 - 27, 2013
Singapore SG
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8th Annual Global Pharma Manufacturing Summit 2013
June 27 - 28, 2013
Boston MA US
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July 2013 [+] (16 total)
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Pharmacovigilance
July 1 - 2, 2013
London UK
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Meeting stability challenges
July 4, 2013
London UK
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Biostatistics for Non-Statisticians
July 8 - 10, 2013
Los Angeles CA US
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Clinical Trial Project Management for Phase 1 thru Phase 4: Best Practices
July 8 - 10, 2013
Los Angeles CA US
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Aseptic Processing in the Manufacture of Biotech and Pharmaceutical Products
July 15 - 16, 2013
King of Prussia PA US
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Medical Devices: EU Directives, Guidance, CE Marking and ISO Standard Certifications
July 15 - 16, 2013
King of Prussia PA US
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Lyophilization Technology – Practical Application of the Scientific Principles
July 15 - 16, 2013
Los Angeles CA US
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4th International Conference on Biomarkers and Clinical Research
July 15 - 17, 2013
Philadelphia PA US
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3rd International Conference on Proteomics & Bioinformatics
July 15 - 17, 2013
Philadelphia PA US
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Comprehensive Overview of FDA Regulatory Compliance for Medical Devices
July 16 - 17, 2013
Los Angeles CA US
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Medical Devices - Developing Effective Post Market Surveillance and Complaint Handling Systems
July 18 - 19, 2013
King of Prussia PA US
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How to Monitor Pharmaceutical, Biologic and Medical Device Clinical Trials for GCP Compliance
July 22 - 23, 2013
Los Angeles CA US
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Recent FDA Approval Trends – What You Should Know
July 22 - 23, 2013
Los Angeles CA US
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GCP Audits - Best Practices for Ensuring Compliance & Detecting Fraud and Misconduct in Clinical Trials
July 29 - 30, 2013
Los Angeles CA US
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2nd International Conference on Nephrology & Therapeutics
July 29 - 31, 2013
Las Vegas NV US
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Constructing World-Class Universities Masterclass Hong Kong & Kuala Lumpur
July 29, 2013 - August 3, 2013
Hong Kong HK
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August 2013 [+] (20 total)
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Development and Validation of Bioanalytical Assays for Biologics: Quantification (PK) and Immunogenicity Assays
August 1 - 2, 2013
King of Prussia PA US
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Good Laboratory Practices for Pre-Clinical Testing
August 5 - 6, 2013
Los Angeles CA US
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Active Pharmaceutical Ingredient (API) and Drug Product Specifications
August 5 - 7, 2013
Los Angeles CA US
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2nd International Conference on Translational Medicine
August 5 - 7, 2013
Chicago IL US
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International Conference on Predictive, Preventive and Personalized Medicine & Molecular Diagnostics
August 5 - 7, 2013
Chicago IL US
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Stability Programs for Product Shelf Life - From Development to Approval
August 8 - 9, 2013
Los Angeles CA US
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The Electronic Common Technical Document (eCTD) - Building Comprehensive Functionality for Effective Implementation
August 12 - 13, 2013
King of Prussia PA US
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Effective Document Management for the Pharmaceutical, Biotech and Medical Device Industries
August 12 - 13, 2013
Los Angeles CA US
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Introduction to Effective Medical Writing
August 12 - 13, 2013
Los Angeles CA US
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2nd International Conference on Biodiversity & Sustainable Energy Development
August 12 - 14, 2013
Raleigh CA US
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8th Annual ImVacS: The Immunotherapeutics and Vaccine Summit
August 13 - 15, 2013
Boston MA US
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International Conference and Exhibition on Physical Medicine & Rehabilitation
August 19 - 21, 2013
Embassy Suites Las Vegas, USA NV US
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International Conference on Dental & Oral Health
August 19 - 21, 2013
Las Vegas NV US
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cGMP Quality Principles for Pharmaceuticals, Biopharmaceuticals, Biologics and Medical Devices
August 19 - 21, 2013
Los Angeles CA US
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Introduction to Molecular Biology Techniques
August 19 - 21, 2013
King of Prussia PA US
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Qualifying and Validating Cloud Computing
August 20 - 21, 2013
San Diego CA US
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International Conference On Molecular Epidemiology and Evolutionary Genetics
August 21 - 23, 2013
Orlando FL US
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Pharmaceutical and Biopharmaceutical Quality Control Laboratories - A Regulatory Compliance Primer
August 22 - 23, 2013
Los Angeles CA US
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2nd International Conference on Tissue Science & Regenerative Medicine
August 26 - 28, 2013
Raleigh NC US
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Biotechnology: Looking Ahead to the 4th Decade
August 27 - 28, 2013
Durham NC US
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September 2013 [+] (25 total)
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Royal Pharmaceutical Society Annual Conference 2013
September 8 - 9, 2013
Birmingham UK
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Validation of Computer Systems
September 9 - 10, 2013
King of Prussia PA US
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Selecting and Managing CROs
September 9 - 10, 2013
King of Prussia PA US
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Clinical Document Management - A Trial by Trial Approach to Compliance
September 11 - 12, 2013
King of Prussia PA US
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Process Validation for Medical Devices
September 11 - 13, 2013
King of Prussia PA US
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Successfully Handling FDA Inspections and ISO Audits for Medical Devices
September 16 - 17, 2013
King of Prussia PA US
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Preparing the CMC Section for NDAs-CTDs-INDs
September 16 - 17, 2013
Los Angeles CA US
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2nd International Conference on Surgery and Anesthesia
September 16 - 18, 2013
Las Vegas NV US
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Freeze Drying Technology - An In-Depth 3-Day Course
September 16 - 18, 2013
Amsterdam
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2013 PDA/FDA Joint Regulatory Conference
September 16 - 18, 2013
Washington DC US
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2nd International Conference on Clinical Microbiol
September 16 - 18, 2013
Las Vegas NV US
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Introduction to Medical Combination Products
September 17 - 18, 2013
King of Prussia PA US
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Effective Internal and External Quality Assurance Auditing for FDA Regulated Industries
September 17 - 18, 2013
Berlin DE
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Big Dip 2013: Big Data in Pharma
September 17 - 20, 2013
London MA US
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Cancer Vaccines
September 18 - 19, 2013
London UK
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ADME, PK/TK, and Drug Metabolism in Drug Discovery and Development
September 18 - 20, 2013
King of Prussia PA US
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Advanced Analytics for Therapeutic Proteins: from Research to Manufacturing
September 18 - 20, 2013
Irsee DE
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2013 PDA/FDA Workshop on Improving Investigations
September 18 - 19, 2013
Washington DC US
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Introduction to Medical Device Submissions - 510ks, PMAs, and Exemptions
September 19 - 20, 2013
King of Prussia PA US
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Comprehensive Overview of FDA Regulatory Compliance for Drug and Biotech Products
September 19 - 20, 2013
Berlin DE
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12th Annual Biological Production Forum 2013
September 23 - 25, 2013
Düsseldorf UK
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Vaccine World China 2013
September 24 - 26, 2013
Hong Kong HK
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3rd World Congress on Cell Science & Stem Cell Research
September 30, 2013 - October 2, 2013
San Antonio TX US
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Pharmaceutical Production Batch Record Review
September 30, 2013 - October 1, 2013
King of Prussia PA US
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International Conference on Psychology, Autism and Alzheimer's Disease
September 30, 2013 - October 1, 2013
San Antonio TX US
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October 2013 [+] (37 total)
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Root Cause Analysis of Failures & Deviations - Developing an Effective CAPA Strategy
October 2 - 4, 2013
King of Prussia PA US
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Japan - Regulatory Filing Requirements and Compliance Processes for Life Sciences
October 3 - 4, 2013
King of Prussia PA US
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Best Practices for an Effective Cleaning Validation Program
October 7 - 8, 2013
King of Prussia PA US
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CMC Regulatory Compliance for Biopharmaceuticals and Biologics
October 7 - 8, 2013
Berlin DE
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Technical Writing for the Pharmaceutical, Medical Device, and Biotech Industries
October 7 - 9, 2013
King of Prussia PA US
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2013 PDA Visual Inspection Forum
October 7 - 8, 2013
Bethesda MD US
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Proactive Compliance Conference
October 7 - 8, 2013
New Brunswick NJ US
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International Conference and Exhibition on Lasers, Optics & Photonics
October 7 - 9, 2013
San Antonio TX US
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Lyophilization Technology - A Comprehensive Course
October 7 - 9, 2013
San Francisco CA US
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2nd International Conference and Exhibition on Materials Science & Engineering
October 7 - 9, 2013
Los Vegas NV US
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Marketing, Advertising and Promotion of Pharmaceuticals and Medical Devices
October 8 - 9, 2013
King of Prussia PA US
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Biosimilars – Understanding the Regulatory Challenges
October 9 - 10, 2013
Berlin DE
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Good Manufacturing Practices
October 9 - 11, 2013
King of Prussia PA US
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Process Validation Intensive
October 9 - 10, 2013
New Brunswick NJ US
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Writing Effective Standard Operating Procedures and Other Process Documents
October 10 - 11, 2013
King of Prussia PA US
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Introduction to Statistical Analysis of Laboratory Data
October 14 - 15, 2013
King of Prussia PA US
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Effective Internal and External Quality Assurance Auditing for FDA Regulated Industries
October 14 - 15, 2013
King of Prussia PA US
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Process Validation for Drugs and Biologics
October 14 - 15, 2013
King of Prussia PA US
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Writing in the Regulated Environment When English Is Your Second Language
October 14 - 15, 2013
King of Prussia PA US
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2nd International Conference on Clinical & Cellular Immunology
October 15 - 17, 2013
Las Vegas NV US
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Comprehensive Overview of FDA Regulatory Compliance for Drug and Biotech Products
October 16 - 17, 2013
King of Prussia PA US
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Effective Risk-Based Applications of Drug cGMPs and Validation Requirements of Cosmetics and OTC Drug Products
October 16 - 17, 2013
King of Prussia PA US
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Clinical Document Management - A Trial by Trial Approach to Compliance
October 21 - 22, 2013
Berlin DE
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How to Monitor Pharmaceutical, Biologic and Medical Device Clinical Trials for GCP Compliance
October 21 - 22, 2013
King of Prussia PA US
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Preparation of FDA Submissions (INDs, NDAs, BLAs, ANDAs, Post-Approval Supplements) and Communicating with the FDA
October 21 - 22, 2013
King of Prussia PA US
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PDA 8th Annual Global Conference on Pharmaceutical Microbiology
October 21 - 23, 2013
Bethesda MD US
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Clinical Trial Project Management for Phase 1 thru Phase 4: Best Practices
October 23 - 25, 2013
Berlin DE
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GCP Audits - Best Practices for Ensuring Compliance & Detecting Fraud and Misconduct in Clinical Trials
October 23 - 24, 2013
King of Prussia PA US
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QA/QC Strategy for Biopharmaceuticals and Biologics
October 23 - 25, 2013
King of Prussia PA US
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2nd International Conference and Exhibition on Probiotics & Functional Foods
October 23 - 25, 2013
Orlando FL US
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Auditing and Qualifying Suppliers and Vendors
October 24 - 25, 2013
Berlin DE
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Design Control for Medical Device Professionals
October 28 - 29, 2013
King of Prussia PA US
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Effective Document Management for the Pharmaceutical, Biotech & Medical Device Industries
October 28 - 29, 2013
Berlin DE
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Analytical Method Validation for Biologics, Biopharmaceuticals and Other Therapeutic Products
October 29 - 30, 2013
King of Prussia PA US
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Design Validation, Verification, and Risk Analysis for Medical Device Professionals
October 30 - 31, 2013
King of Prussia PA US
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Aseptic Processing in the Manufacture of Biotech and Pharmaceutical Products
October 31, 2013 - November 1, 2013
King of Prussia PA US
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CMC Regulatory Compliance for Biopharmaceuticals and Biologics
October 31, 2013 - November 1, 2013
King of Prussia PA US
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November 2013 [+] (26 total)
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2013 ISPE Annual Meeting
November 3 - 6, 2013
Washington DC US
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ADME, PK/TK, and Drug Metabolism in Drug Discovery and Development
November 4 - 6, 2013
Berlin DE
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Biosimilars – Understanding the Regulatory Challenges
November 4 - 5, 2013
King of Prussia PA US
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Clinical Trial Design for Medical Devices
November 4 - 5, 2013
Los Angeles CA US
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Medical Devices: EU Directives, Guidance, CE Marking and ISO Standard Certifications
November 4 - 5, 2013
Los Angeles CA US
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Recent FDA Approval Trends – What You Should Know
November 4 - 5, 2013
Berlin DE
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The EU Clinical Trial Directive
November 4 - 5, 2013
King of Prussia PA US
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Pediatric Clinical Trial Design
November 6 - 7, 2013
Los Angeles CA US
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Navigating Latin American Regulatory Compliance Requirements for Clinical Trials
November 6 - 7, 2013
Los Angeles CA US
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The Drug Development Process - From Discovery to Commercialization
November 6 - 8, 2013
King of Prussia PA US
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Lyophilization Technology – Practical Application of the Scientific Principles
November 7 - 8, 2013
King of Prussia PA US
Read more... -
Medical Devices - Developing Effective Post Market Surveillance and Complaint Handling Systems
November 7 - 8, 2013
Los Angeles CA US
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Adverse Drug Events – Understanding and Reporting Requirements
November 11 - 12, 2013
King of Prussia PA US
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Cleanroom Microbiology for the Non-Microbiologist
November 11 - 12, 2013
King of Prussia PA US
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Process Validation for Drugs and Biologics
November 11 - 12, 2013
Berlin DE
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2nd International Summit on GLP, GCP & Clinical
November 12 - 14, 2013
Skokie IL US
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PDA/FDA Advanced Technologies for Virus Detection in the Evaluation of Biologicals Conference
November 13 - 14, 2013
Bethesda MD US
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Process Validation for Medical Devices
November 13 - 15, 2013
Berlin DE
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Good Manufacturing Practices
November 13 - 15, 2013
Berlin DE
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Sterilization Procedures: Introduction to the Science and Methods
November 13 - 14, 2013
King of Prussia PA US
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Comprehensive Overview of European Regulatory Procedures - EU and Member State Submission Requirements
November 14 - 15, 2013
Berlin DE
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Advanced Topics in Biostatistics for Non-Statisticians
November 14 - 15, 2013
King of Prussia PA US
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Comprehensive Overview of FDA Regulatory Compliance for Medical Devices
November 18 - 19, 2013
King of Prussia PA US
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Freeze Drying: 2-Day Product and Process Course
November 18 - 19, 2013
Dublin
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Pharmtech
November 25 - 28, 2013
Moscow RU
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Pharmingredients+
November 25 - 28, 2013
Moscow RU
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December 2013 [+] (15 total)
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2nd International Conference and Exhibition on Obesity & Weight Management
December 2 - 4, 2013
Las Vegas NV US
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Pharmaceutical Production Batch Record Review
December 2 - 3, 2013
Berlin DE
Read more... -
The Electronic Common Technical Document (eCTD) - Building Comprehensive Functionality for Effective Implementation
December 2 - 3, 2013
King of Prussia PA US
Read more... -
cGMP Quality Principles for Pharmaceuticals, Biopharmaceuticals, Biologics and Medical Devices
December 2 - 4, 2013
King of Prussia PA US
Read more... -
FDA Inspections: What Regulators Expect and How to Prepare
December 4 - 5, 2013
Berlin DE
Read more... -
Development and Validation of Bioanalytical Assays for Biologics: Quantification (PK) and Immunogenicity Assays
December 5 - 6, 2013
Los Angeles CA US
Read more... -
Introduction to Effective Medical Writing
December 5 - 6, 2013
Berlin DE
Read more... -
Good Laboratory Practices for Pre-Clinical Testing
December 9 - 11, 2013
King of Prussia PA US
Read more... -
Preparing the CMC Section for NDAs-CTDs-INDs
December 9 - 10, 2013
King of Prussia PA US
Read more... -
Validation of Computer Systems
December 9 - 10, 2013
Los Angeles CA US
Read more... -
Stability Programs for Product Shelf Life - From Development to Approval
December 9 - 10, 2013
Berlin DE
Read more... -
Technical Writing for the Pharmaceutical, Medical Device, and Biotech Industries
December 9 - 11, 2013
Berlin DE
Read more... -
Freeze Drying: 2-Day Product and Process Course
December 10 - 11, 2013
Winchester
Read more... -
Active Pharmaceutical Ingredient (API) and Drug Product Specifications
December 11 - 13, 2013
Berlin DE
Read more... -
Writing Effective Standard Operating Procedures and Other Process Documents
December 12 - 13, 2013
Berlin DE
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