Events Calendar
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Events By Name
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Upcoming Events
- May 17, 2012 - Analytical Test Methods Validation: FDA, ICH and USP Requirements
- May 17 - 18, 2012 - HIPAA Privacy, Security and Breach Notification Compliance: Understanding the Requirements, Preventing Incidents, Surviving Audits, and Avoiding
- May 20 - 23, 2012 - Oligonucleotide Therapeutics Discovery & Peptide Discovery and Development
- May 20 - 23, 2012 - TIDES: Oligonucleotides and Peptide Technology & Product Development & Applications of Nucleic Acids Technologies in Molecular Diagnostics
- May 22, 2012 - Supplier Controls to Meet Tougher U.S. FDA Requirements
Events By Month
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May 2012 [+] (15 total)
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Validation and 21 CFR Part 11 Compliance of Computer Systems - US Seminar 2012 at San Francisco
May 3 - 4, 2012
San Francisco, Marriott Marquis Downtown CA US
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Raw Materials Risk Management in GMP Facilities: Avoiding GMP non-Compliance Due to Raw Material Issues
May 3, 2012
Palo Alto CA US
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FDA Software Validation Self-Check – plan an effective Internal Audit program
May 9, 2012
Palo Alto CA US
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Process Analytical Technology (PAT) is more than it Seems - US Seminar 2012 at San Francisco
May 10 - 11, 2012
San Francisco, Marriott Marquis Downtown CA US
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Logical Water System Validation - Webinar By ComplianceOnline
May 11, 2012
Palo Alto CA US
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Equipment Calibration in FDA QSR – Regulations and Warning Letters
May 11, 2012
Palo Alto CA US
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Analytical Test Methods Validation: FDA, ICH and USP Requirements
May 17, 2012
Palo Alto CA US
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HIPAA Privacy, Security and Breach Notification Compliance: Understanding the Requirements, Preventing Incidents, Surviving Audits, and Avoiding
May 17 - 18, 2012
Boston MA US
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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 US
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Oligonucleotide Therapeutics Discovery & Peptide Discovery and Development
May 20 - 23, 2012
Las Vegas NV US
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Supplier Controls to Meet Tougher U.S. FDA Requirements
May 22, 2012
Palo Alto CA US
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FDA Warning Letter - Consent Decree Software Validation
May 23, 2012
Palo Alto CA US
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Statistics for the Non-Statistician - US Seminar 2012 at Washington DC
May 24 - 25, 2012
Marriott Washington, DC 8 AM to 5 PM EDT WA US
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Pre-Approval Statements and Representations by Pharmaceutical Manufacturers
May 24, 2012
Palo Alto CA US
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Risk-Based Validation Equipment Validation - Webinar By ComplianceOnline
May 31, 2012
Palo Alto CA US
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June 2012 [+] (13 total)
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Single Use Applications for Biopharmaceutical Manufacturing
June 4 - 6, 2012
San Francisco MA US
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Vaccine Production Summit
June 4 - 6, 2012
San Francisco CA US
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ICH Q10; moving from GMPs to a Pharmaceutical Quality System
June 5, 2012
Palo Alto CA US
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Cell Line Development and Engineering
June 6 - 8, 2012
San Francisco CA US
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Global Pharma Manufacturing Summit 2012
June 11 - 12, 2012
New Jersey NJ US
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4th Annual Drug Development Summit 2012
June 11 - 12, 2012
Zurich CH
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13th Drug Discovery Summit 2012
June 11 - 12, 2012
Zurich CH
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FDA Warning Letter Closeout Program
June 12, 2012
Palo Alto CA US
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Reduce COTS Software Validation using the risk-based approach
June 19, 2012
Palo Alto CA US
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Next Generation Protein Therapeutics Summit
June 25 - 27, 2012
San Francisco CA US
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FDA's new enforcement initiative – Strategic Software Validation Planning for Executives and Managers
June 27, 2012
Palo Alto CA US
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FDA's new enforcement initiative – Strategic Software Validation Planning for Executives and Managers
June 27, 2012
Palo Alto CA US
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Full Day Virtual Seminar: Understanding and Effectively Controlling Biofilm in Pharmaceutical Water Systems
June 28, 2012
Palo Alto CA US
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July 2012 [+] (2 total)
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GAMP® 5 as applied to FDA software validation - strategies to avoid warning letters
July 11, 2012
Palo Alto CA US
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Software validation and 21 CFR Part 11 remediation planning: FDA inspection strategies
July 25, 2012
Palo Alto CA US
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August 2012 [+] (6 total)
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Translating Biology to the Clinic
August 6 - 8, 2012
San Francisco CA US
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Antibody Drug Development
August 6 - 8, 2012
San Francisco CA US
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Clinical Biomarkers and Cancer
August 6 - 8, 2012
San Francisco MA US
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Diagnostic Development
August 6 - 8, 2012
San Francisco CA US
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Spreadsheet Validation: Understanding and satisfying FDA requirements
August 8, 2012
Palo Alto CA US
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The 6 Most Common Problems in FDA Software Validation & Verification
August 22, 2012
Palo Alto CA US
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September 2012 [+] (4 total)
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Validation and use of Excel spreadsheets in FDA regulated environments
September 5, 2012
Palo Alto CA US
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Cell Therapy Bioprocessing
September 10 - 11, 2012
National Harbor MD US
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Biopharma Asia Congress 2012
September 10 - 11, 2012
Singapore SG
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Risk Assessment-Compliance Using Easy To Fill Out Documentation
September 18, 2012
Palo Alto CA US
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October 2012 [+] (5 total)
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BioProcess International Conference & Exhibition
October 7 - 12, 2012
Providence RI US
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Oncology Clinical Development Congress
October 10 - 11, 2012
Manchester UK
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2nd Annual Oncology Biomarkers Congress
October 10 - 11, 2012
Manchester UK
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Well Characterized Biologicals
October 30, 2012 - November 1, 2012
Washington DC US
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Process 2 Product
October 31, 2012 - November 1, 2012
Washington DC US
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December 2012 [+] (1 total)
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Antibody Engineering & Antibody Therapeutics
December 2 - 6, 2012
San Diego CA US
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