Events Calendar
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Events By Name
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Upcoming Events
- February 13 - 14, 2012 - Clinical Trials & Outsourcing Asia Congress 2012
- February 13 - 14, 2012 - 2nd Pharma R&D Asia Congress
- February 14 - 15, 2012 - Marketing, Advertising and Promotion of Pharmaceuticals and Medical Devices
- February 15 - 16, 2012 - FDA Inspections -What Regulators Expect and How to Prepare
- February 21 - 22, 2012 - 7th Annual Biomarkers Congress 2012
Events By Month
Click on a month below to view its associated events.
February 2012 [+] (42 total)
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The Drug Development Process - from Discovery to Commercialization
February 1 - 3, 2012
King of Prussia PA UNITED STATES
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Efficient Computer System Validation - 10 Easy Steps - Webinar By GlobalCompliancePanel
February 1, 2012
Online Training DE UNITED STATES
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Residual Moisture Testing - Proven Techniques - Webinar By GlobalCompliancePanel
February 1, 2012
Online Training DE UNITED STATES
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Risk Analysis for Portfolio of Drug Development Programs - Webinar By GlobalCompliancePanel
February 2, 2012
Online Training DE UNITED STATES
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Effective Internal and External Quality Assurance Auditing for FDA Regulated Industries
February 2 - 3, 2012
King of Prussia PA UNITED STATES
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SLAS2012, First Annual Conference & Exhibition
February 4 - 8, 2012
San Diego CA UNITED STATES
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SLAS2012, the First Annual Conference & Exhibition
February 4 - 8, 2012
San Diego CA UNITED STATES
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Analytical Method Validation for Biologics, Biopharmaceuticals and Other Therapeutic Products
February 6 - 7, 2012
King of Prussia PA UNITED STATES
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Good Clinical Practices (GCPs)
February 6 - 8, 2012
King of Prussia PA UNITED STATES
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Practical Methods for Project Management
February 6 - 7, 2012
Los Angeles CA UNITED STATES
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Life Sciences Internal Audit Forum
February 7 - 9, 2012
Philadelphia PA UNITED STATES
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QA/QC Strategy for Biologics and Biopharmaceuticals
February 8 - 10, 2012
King of Prussia PA UNITED STATES
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Product Risk Management Under ISO 14971 and FDA-ICH Q9 - Webinar By GlobalCompliancePanel
February 8, 2012
Online Training DE UNITED STATES
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Life Cycle Validation of GMP Potency Bioassays
February 9, 2012
Palo Alto CA UNITED STATES
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Adverse Drug Events – Reporting and Regulatory Requirements
February 9 - 10, 2012
King of Prussia PA UNITED STATES
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Effective Laboratory Safety Management
February 9 - 10, 2012
Los Angeles CA UNITED STATES
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Clinical Trials & Outsourcing Asia Congress 2012
February 13 - 14, 2012
Shanghai, China CHINA
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2nd Pharma R&D Asia Congress
February 13 - 14, 2012
Shanghai CHINA
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Marketing, Advertising and Promotion of Pharmaceuticals and Medical Devices
February 14 - 15, 2012
King of Prussia PA UNITED STATES
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FDA Inspections -What Regulators Expect and How to Prepare
February 15 - 16, 2012
King of Prussia PA UNITED STATES
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Risk Assessment - Compliance Using Easy To Fill Out Documentation - Webinar By GlobalCompliancePanel
February 21, 2012
Online Training DE UNITED STATES
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Dietary Supplement Regulatory Compliance in the United States: Labeling, Product Claims & Updates from the FDA - Webinar By GlobalCompliancePanel
February 21, 2012
Wilmington DE UNITED STATES
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7th Annual Biomarkers Congress 2012
February 21 - 22, 2012
Manchester UNITED KINGDOM
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1st Annual CNS Biomarkers Congress 2012
February 21 - 22, 2012
Manchester UNITED KINGDOM
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Implement a Tougher Supplier Audit Program - Webinar By GlobalCompliancePanel
February 22, 2012
Online Training DE UNITED STATES
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Accelerating Bioassay Transfer in a GMP Environment
February 23, 2012
Palo Alto CA UNITED STATES
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Biostatistics for Non-Statisticians
February 27 - 29, 2012
King of Prussia PA UNITED STATES
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Lyophilization Technology - Practical Application of the Scientific Principles
February 27 - 29, 2012
King of Prussia PA UNITED STATES
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IBC's Process & Product Validation
February 27 - 29, 2012
San Diego CA UNITED STATES
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IBC's Outsourcing Manufacturing of Biopharmaceuticals
February 27 - 28, 2012
San Diego CA UNITED STATES
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IBC's Technology Transfer for Biopharmaceuticals
February 27 - 28, 2012
San Diego CA UNITED STATES
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Biopharmaceutical Raw Materials throughout the Product Lifecycle
February 27 - 28, 2012
San Diego CA UNITED STATES
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Viral Safety for Biologicals
February 27 - 28, 2012
San Diego CA UNITED STATES
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Biophrmaceutical Development & Production Week
February 27, 2012 - March 2, 2012
San Diego CA UNITED STATES
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Biopharmaceutical Development & Production Week
February 27, 2012 - March 2, 2012
San Diego CA UNITED STATES
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Lessons from 483s
February 27 - 28, 2012
Tampa FL UNITED STATES
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AsiaTIDES: Oligonucleotide and Peptide Research, Technology and Product Development
February 28, 2012 - March 1, 2012
Tokyo JAPAN
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The Global Evolution of Aseptic Processing
February 29, 2012 - March 1, 2012
Tampa FL UNITED STATES
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IBC's Biosimilars and Biobetters: Technologies & Development Strategies
February 29, 2012 - March 2, 2012
San Diego MA UNITED STATES
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IBC's Antibody Development & Production
February 29, 2012 - March 2, 2012
San Diego CA UNITED STATES
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IBC's Analytical Technologies for Biotherapeutic Development
February 29, 2012 - March 2, 2012
San Diego CA UNITED STATES
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IBC's Recombinant Protein & Complex Biologic Development & Production
February 29, 2012 - March 2, 2012
San Diego CA UNITED STATES
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March 2012 [+] (37 total)
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Clinical Document Management - A Trial by Trial Approach to Compliance
March 1 - 2, 2012
Los Angeles CA UNITED STATES
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Introduction to Statistical Analysis of Laboratory Data
March 1 - 2, 2012
King of Prussia PA UNITED STATES
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Preparation of FDA Submissions and Communicating with the FDA (INDs, NDAs, BLAs, ANDAs, ABLAs, Post-Approval Supplements)
March 5 - 6, 2012
King of Prussia PA UNITED STATES
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Introduction to Molecular Biology Techniques - Applications in the Biotechnology and Pharmaceutical Industries
March 5 - 7, 2012
King of Prussia PA UNITED STATES
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Introduction to Medical Combination Products
March 5 - 6, 2012
Los Angeles CA UNITED STATES
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Cleanroom Microbiology for the Non-Microbiologist
March 5 - 6, 2012
King of Prussia PA UNITED STATES
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21 CFR Part 11 and Annex 11; What you Need to Know to Pass the New Regulatory Audits - Webinar By GlobalCompliancePanel
March 6, 2012
Wilmington DE UNITED STATES
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DHF, DMR, DHR, and the Technical File-Design Dossier - Similarities and Differences - Webinar By GlobalCompliancePanel
March 7, 2012
Wilmington DE UNITED STATES
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Introduction to Medical Device Submissions - 510ks, PMAs, and Exemptions
March 7 - 8, 2012
Los Angeles PA UNITED STATES
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Sterilization Procedures Technology, Equipment & Validation
March 7 - 8, 2012
King of Prussia PA UNITED STATES
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Validation of Computer Systems
March 8 - 9, 2012
King of Prussia PA UNITED STATES
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Managing Immunogenicity Risk in Biopharmaceuticals
March 8, 2012
Palo Alto CA UNITED STATES
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Design Control for Medical Device Professionals
March 12 - 13, 2012
Los Angeles CA UNITED STATES
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Vaccine World Summit
March 12 - 16, 2012
Hyderabad INDIA
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Changes in the EU Medical Device Directives; 2010 Modifications and the 2012 Recast of the MDD Directives - Webinar By GlobalCompliancePanel
March 13, 2012
Wilmington DE UNITED STATES
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Auditing Computer Systems for FDA and International Compliance - Webinar By GlobalCompliancePanel
March 13, 2012
Wilmington DE UNITED STATES
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The Drug Development Process - from Discovery to Commercialization
March 14 - 16, 2012
Berlin GERMANY
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Biostatistics for Non-Statisticians
March 14 - 16, 2012
Berlin GERMANY
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Design Validation, Verification, and Risk Analysis for Medical Device Professionals
March 14 - 15, 2012
Los Angeles CA UNITED STATES
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Preparing the CMC Section for NDAs/INDs/CTDs
March 15 - 16, 2012
Los Angeles CA UNITED STATES
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Good Clinical Practices (GCPs)
March 19 - 21, 2012
Berlin GERMANY
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cGMP Quality Principles for Pharmaceuticals, Biopharmaceuticals, Biologics and Medical Devices
March 19 - 21, 2012
Dublin IRELAND
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Selecting and Managing CROs
March 19 - 20, 2012
Los Angeles CA UNITED STATES
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Lyophilization Technology - Practical Application of the Scientific Principles
March 20 - 22, 2012
Dublin IRELAND
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Excel Spreadsheet Validation to Eliminate 483s - Webinar By GlobalCompliancePanel
March 20, 2012
Wilmington DE UNITED STATES
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The 510(k) Submission: Requirements, Contents, and Options - Webinar By GlobalCompliancePanel
March 20, 2012
Online Training DE UNITED STATES
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Master Verification & Validation Planning under U.S. FDA CGMP, ICH Q-series and ISO 13485-14971 Requirements - Webinar By GlobalCompliancePanel
March 21, 2012
Online Training DE UNITED STATES
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Writing Effective Standard Operating Procedures and Other Process Documents
March 22 - 23, 2012
King of Prussia PA UNITED STATES
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Aseptic Processing in the Manufacture of Biotech and Pharmaceutical Products
March 26 - 27, 2012
Los Angeles CA UNITED STATES
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Writing in the Regulated Environment When English Is Your Second Language
March 26 - 27, 2012
King of Prussia PA UNITED STATES
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Pharmaceutical Production Batch Record Review
March 26 - 27, 2012
Los Angeles CA UNITED STATES
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Project Management for Phase 1 & 2 Clinical Trials
March 26 - 27, 2012
King of Prussia PA UNITED STATES
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Process Validation for Drugs and Biologics
March 26 - 27, 2012
Dublin IRELAND
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Comprehensive Overview of FDA Regulatory Compliance for Medical Devices
March 28 - 29, 2012
Dublin IRELAND
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Project Management for Phase 3 and LCM (Life Cycle Management) of the Drug Development Process
March 28 - 29, 2012
King of Prussia PA UNITED STATES
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Technical Writing for the Pharmaceutical, Medical Device, and Biotech Industries
March 28 - 30, 2012
King of Prussia PA UNITED STATES
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EU Filing and Registration Procedures
March 29 - 30, 2012
Dublin IRELAND
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April 2012 [+] (21 total)
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2nd Annual Vaccines Congress 2012
April 2 - 3, 2012
London UNITED KINGDOM
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5th Annual Proteins Congress 2012
April 2 - 3, 2012
London UNITED KINGDOM
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How to Monitor Pharmaceutical, Biologic and Medical Device Clinical Trials for GCP Compliance
April 2 - 3, 2012
King of Prussia PA UNITED STATES
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Japan - Regulatory Filing Requirements and Compliance Processes for Life Sciences
April 2 - 3, 2012
Los Angeles CA UNITED STATES
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Quality System Regulation for the Medical Device & Biotech Industries
April 2 - 3, 2012
King of Prussia PA UNITED STATES
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GCP Audits - Best Practices for Ensuring Compliance & Detecting Fraud and Misconduct in Clinical Trials
April 4 - 5, 2012
King of Prussia PA UNITED STATES
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Development and Validation of Bioanalytical Assays for Biologics: Quantification (PK) and Immunogenicity Assays
April 12 - 13, 2012
Berlin GERMANY
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Bioprocess Training Academy
April 16 - 17, 2012
Boston MA UNITED STATES
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2012 PDA Annual Meeting
April 16 - 18, 2012
Phoenix AZ UNITED STATES
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PDA Single Use Systems Workshop
April 18 - 19, 2012
Bethesda MD UNITED STATES
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Effective Document Management for the Pharmaceutical, Biotech and Medical Device Industries
April 19 - 20, 2012
Berlin GERMANY
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Analytical Method Validation for Biologics, Biopharmaceuticals and Other Therapeutic Products
April 23 - 24, 2012
Berlin GERMANY
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Active Pharmaceutical Ingredient (API) and Drug Product Specifications
April 23 - 25, 2012
King of Prussia PA UNITED STATES
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Process Validation for Medical Devices
April 23 - 25, 2012
Los Angeles PA UNITED STATES
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Technical Writing for the Pharmaceutical, Medical Device, and Biotech Industries
April 23 - 25, 2012
Berlin GERMANY
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QA/QC Strategy for Biopharmaceuticals and Biologics
April 25 - 27, 2012
Berlin GERMANY
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How to Implement Risk Management Principles and Activities Within A Quality Management System
April 26 - 27, 2012
Los Angeles CA UNITED STATES
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Stability Programs for Product Shelf Life - From Development to Approval
April 26 - 27, 2012
King of Prussia PA UNITED STATES
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Writing Effective Standard Operating Procedures and Other Process Documents
April 26 - 27, 2012
Berlin GERMANY
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Biological Assay Development, Validation & Maintenance
April 30, 2012 - May 2, 2012
Boston MA UNITED STATES
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IBC’s 22nd International Biological Assay Conference
April 30, 2012 - May 2, 2012
Boston MA UNITED STATES
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May 2012 [+] (20 total)
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Best Practices For An Effective Cleaning Validation Program
May 1 - 2, 2012
Los Angeles CA UNITED STATES
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Root Cause Analysis of Failures & Deviations - Developing an Effective CAPA Strategy
May 2 - 4, 2012
King of Prussia PA UNITED STATES
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Process Validation for Drugs and Biologics
May 3 - 4, 2012
Los Angeles CA UNITED STATES
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Validation of Computer Systems
May 7 - 8, 2012
Berlin GERMANY
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The Drug Development Process - From Discovery to Commercialization
May 14 - 16, 2012
Los Angeles CA UNITED STATES
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PDA Chemistry Manufacturing & Controls (CMC) Workshop
May 14, 2012
Bethesda MD UNITED STATES
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Medical Devices – EU Directives Guidance CE Marking and ISO Standard Certifications
May 14 - 15, 2012
Dublin IRELAND
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PDA/FDA Virus and TSE Safety Conference
May 15 - 17, 2012
Bethesda MD UNITED STATES
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Effective Internal and External Quality Assurance Auditing for FDA Regulated Industries
May 15 - 16, 2012
Los Angeles CA UNITED STATES
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Practical Methods for Project Management
May 16 - 17, 2012
Dublin IRELAND
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ADME, PK/TK, and Drug Metabolism in Drug Discovery and Development
May 16 - 18, 2012
Los Angeles CA UNITED STATES
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Auditing and Qualifying Suppliers and Vendors - An Effective Risk Based Approach
May 17 - 18, 2012
Los Angeles PA UNITED STATES
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Medical Devices – Developing Effective Post Market Surveillance and Complaint Handling Systems
May 17 - 18, 2012
Dublin IRELAND
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TIDES: Oligonucleotides and Peptide Technology & Product Development & Applications of Nucleic Acids Technologies in Molecular Diagnostics
May 20 - 23, 2012
Las Vegas NV UNITED STATES
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Oligonucleotide Therapeutics Discovery & Peptide Discovery and Development
May 20 - 23, 2012
Las Vegas NV UNITED STATES
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Medical Devices – Field Actions and Their Management - Recalls, Product Recovery, Safety Alert
May 21 - 22, 2012
Dublin IRELAND
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FDA Inspections -What Regulators Expect and How to Prepare
May 21 - 22, 2012
Dublin IRELAND
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The EU Clinical Trial Directive
May 21 - 22, 2012
King of Prussia PA UNITED STATES
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Writing Effective Standard Operating Procedures and Other Process Documents
May 21 - 22, 2012
Los Angeles CA UNITED STATES
Read more... -
Effective Document Management for the Pharmaceutical, Biotech and Medical Device Industries
May 23 - 24, 2012
Los Angeles CA UNITED STATES
Read more...
June 2012 [+] (25 total)
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Good Clinical Practices (GCPs)
June 4 - 6, 2012
Los Angeles CA UNITED STATES
Read more... -
Practical Methods for Project Management
June 4 - 5, 2012
King of Prussia PA UNITED STATES
Read more... -
PDA/FDA Glass Quality Conference
June 4 - 5, 2012
Bethesda MD UNITED STATES
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Vaccine Production Summit
June 4 - 6, 2012
San Francisco CA UNITED STATES
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Single Use Applications for Biopharmaceutical Manufacturing
June 4 - 6, 2012
San Francisco CA UNITED STATES
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Cell Line Development and Engineering
June 6 - 8, 2012
San Francisco CA UNITED STATES
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Adverse Drug Events – Understanding and Reporting Requirements
June 7 - 8, 2012
Los Angeles CA UNITED STATES
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The Electronic Common Technical Document (eCTD) - Building Comprehensive Functionality for Effective Implementation
June 11 - 12, 2012
King of Prussia PA UNITED STATES
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Validation of Computer Systems
June 11 - 12, 2012
Los Angeles CA UNITED STATES
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Analytical Method Validation for Biologics, Biopharmaceuticals and Other Therapeutic Products
June 11 - 12, 2012
Los Angeles CA UNITED STATES
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DDI-2012: 15th International Conference on Drug-drug Interactions
June 11 - 13, 2012
Seattle WA UNITED STATES
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4th Annual Drug Development Summit 2012
June 11 - 12, 2012
Zurich SWITZERLAND
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13th Drug Discovery Summit 2012
June 11 - 12, 2012
Zurich SWITZERLAND
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FDA Inspections -What Regulators Expect and How to Prepare
June 12 - 13, 2012
Los Angeles CA UNITED STATES
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QA/QC Strategy for Biopharmaceuticals and Biologics
June 13 - 15, 2012
Los Angeles CA UNITED STATES
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ETS-2012: 10th International Conference on Early Toxicity Screening
June 14 - 15, 2012
Seattle WA UNITED STATES
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Preparation of FDA Submissions (INDs, NDAs, BLAs, ANDAs, Post-Approval Supplements)and Communicating with the FDA
June 18 - 19, 2012
Los Angeles CA UNITED STATES
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2012 PDA Innovation and Best Practices on Sterile Technology Conference
June 18 - 19, 2012
Chicago IL UNITED STATES
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Comprehensive Overview of FDA Regulatory Compliance for Medical Devices
June 19 - 20, 2012
King of Prussia PA UNITED STATES
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CMC Regulatory Compliance for Biopharmaceuticals and Biologics
June 20 - 22, 2012
Los Angeles CA UNITED STATES
Read more... -
Lyophilization Technology - Practical Application of the Scientific Principles
June 25 - 27, 2012
Los Angeles CA UNITED STATES
Read more... -
Project Management for Phase 1 & 2 Clinical Trials
June 25 - 26, 2012
Los Angeles CA UNITED STATES
Read more... -
Preparing the CMC Section for NDAs-CTDs-INDs
June 25 - 26, 2012
King of Prussia PA UNITED STATES
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Next Generation Protein Therapeutics Summit
June 25 - 27, 2012
San Francisco CA UNITED STATES
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Project Management for Phase 3 and LCM (Life Cycle Management) of the Drug Development Process
June 27 - 28, 2012
Los Angeles CA UNITED STATES
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July 2012 [+] (11 total)
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Introduction to Effective Medical Writing
July 9 - 10, 2012
Los Angeles CA UNITED STATES
Read more... -
Biostatistics for Non-Statisticians
July 9 - 11, 2012
Los Angeles PA UNITED STATES
Read more... -
Technical Writing for the Pharmaceutical, Medical Device, and Biotech Industries
July 11 - 13, 2012
Los Angeles CA UNITED STATES
Read more... -
Pharmaceutical Production Batch Record Review
July 16 - 17, 2012
King of Prussia PA UNITED STATES
Read more... -
Aseptic Processing in the Manufacture of Biotech and Pharmaceutical Products
July 16 - 17, 2012
King of Prussia PA UNITED STATES
Read more... -
Medical Devices – EU Directives Guidance CE Marking and ISO Standard Certifications
July 16 - 17, 2012
King of Prussia PA UNITED STATES
Read more... -
Medical Devices – Developing Effective Post Market Surveillance and Complaint Handling Systems
July 19 - 20, 2012
King of Prussia PA UNITED STATES
Read more... -
How to Monitor Pharmaceutical, Biologic and Medical Device Clinical Trials for GCP Compliance
July 23 - 24, 2012
Los Angeles CA UNITED STATES
Read more... -
European Filing and Registration Procedures
July 23 - 24, 2012
King of Prussia PA UNITED STATES
Read more... -
Medical Devices – Field Actions and Their Management - Recalls, Product Recovery and Safety Alerts
July 23 - 24, 2012
King of Prussia PA UNITED STATES
Read more... -
GCP Audits - Best Practices for Ensuring Compliance & Detecting Fraud and Misconduct in Clinical Trials
July 30 - 31, 2012
Los Angeles CA UNITED STATES
Read more...
August 2012 [+] (2 total)
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Translating Biology to the Clinic
August 6 - 8, 2012
San Francisco MA UNITED STATES
Read more... -
Diagnostic Development
August 6 - 8, 2012
San Francisco CA UNITED STATES
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September 2012 [+] (3 total)
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Cell Therapy Bioprocessing
September 10 - 11, 2012
National Harbor MD UNITED STATES
Read more... -
2012 PDA/FDA Joint Regulatory Conference
September 10 - 12, 2012
Bethesda MD UNITED STATES
Read more... -
Biooharma Asia Congress 2012
September 10 - 11, 2012
Singapore SINGAPORE
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October 2012 [+] (9 total)
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BioProcess International Conference & Exhibition
October 7 - 12, 2012
Providence RI UNITED STATES
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PDA Biennial Training Conference
October 8 - 9, 2012
Bethesda MD UNITED STATES
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Formulation Strategies for Protein Therapeutics
October 9 - 11, 2012
Providence RI UNITED STATES
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2nd Annual Oncology Biomarkers Congress
October 10 - 11, 2012
Manchester UNITED KINGDOM
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Oncology Clinical Development Congress
October 10 - 11, 2012
Manchester UNITED KINGDOM
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The Universe of Pre-filled Syringes & Injection Devices
October 15 - 17, 2012
Las Vegas NV UNITED STATES
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PDA’s 7th Annual Global Conference on Pharmaceutical Microbiology
October 22 - 24, 2012
Bethesda MD UNITED STATES
Read more... -
Well Characterized Biologicals
October 30, 2012 - November 1, 2012
Washington DC UNITED STATES
Read more... -
Process 2 Product
October 30, 2012 - November 1, 2012
Washington DC UNITED STATES
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November 2012 [+] (2 total)
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PDA/FDA Pharmaceutical Supply Chain Conference
November 13 - 14, 2012
Bethesda MD UNITED STATES
Read more... -
2012 Pharmaceutical Cold Chain & Good Distribution Practice Conference
November 15 - 16, 2012
Bethesda MD UNITED STATES
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December 2012 [+] (2 total)
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Antibody Engineering & Antibody Therapeutics
December 2 - 6, 2012
San Diego CA UNITED STATES
Read more... -
PDA/FDA Vaccines Conference
December 3 - 4, 2012
Bethesda MD UNITED STATES
Read more...
January 2013 [+] (0 total)
February 2013 [+] (0 total)
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