Wednesday March 10, 2010






IPA 2010 Upcoming Events

6th Annual Stability Testing Conference
Pharmaceutical and Biopharmaceutical Stability:
Current Trends and Best Practices to Support Global Markets

March 23-24, 2010

Somerset, NJ - USA

 

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The CTD and eCTD Formats for NDA & BLA Submissions

March 23-24, 2010

Philadelphia, USA

 

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New addition to Health Canada’s GMP regulation
Annual Product Quality Review (APQR) and Annual Product Review (APR)

March 24-25, 2010

Toronto, Canada

 

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Quality Risk Management

March 30-31, 2010

Somerset, NJ, USA

Workshops, Case Studies & Interactive Exercises

 

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Refresher Training Course on
GMP regulations and guidelines

March 30-31, 2010

Vancouver, Canada

Build Excellence & Strengthen your Workforce

Refresh your Good Manufacturing Practice (GMP) awareness in manufacturing and packaging.

 

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Leadership Workshop

March 30-31, 2010

Montreal, Canada

 

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Good Documentation Practices for GMP operations
Ensuring Regulatory Compliance & Best Practices in GMP Operations For Pharmaceutical and Biopharmaceutical Industries

March 30-31, 2010

Montreal, Canada

 

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Process Validation for the 21st Century
for Biological and pharmaceutical

March 30-31 2010

Philadelphia, USA

 

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TO BE ANNOUNCED...

Investigating Out-of-Specification (OOS) Results

for Pharmaceutical, Biotechnology, Medical Devices and Allied Industries

March 2-3, 2010

Montreal, Canada

Pharmaceutical Microbiology & Best Practices
Addressing the most pressing issues in pharmaceutical microbiology

April 7-8, 2010

Toronto, Canada

 

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Implementation of Effective & Compliant CAPA Programs

April 7-8, 2010

Somerset, New Jersey

 

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Computer Systems Validation
in the Pharmaceutical & Biotech Industries

April 14-15, 2010

Montreal, Canada

Strategy for Simplifying the Computer Systems Validation Process to Maximize Compliance and Reduce; cost, effort, time, and documentation

 

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GMP Chapter
Effective Quality Assurance Auditing

April 14-15, 2010

Montreal, Canada

 

 

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Cleaning Validation Practices

April 14-15, 2010

Montreal, Canada

 

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Project Management

April 14-15, 2010

Montreal, Canada

 

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Designing Pharmaceutical GMP Facilities

April 20-21, 2010

China

 

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Environmental Monitoring (EM) in Pharmaceutical Manufacturing

April 20-21, 2010

New Jersey/New York

 

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Generic Drug Submissions and Approval

April 20-21, 2010

New Jersey, USA

 

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Natural Health Products & Dietary Supplements

April 21-22, 2010

Montreal, Canada

 

 

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Residual Solvents Testing
Interpreting and Implementing ICH Q3C Requirements; Strategies to Meet New USP Residual Solvent Requirements

April 21-22, 2010

Toronto, Canada

 

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Aseptic Processing Operations

April 26-27, 2010

Philadelphia, PA

 

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Adverse Drug Event Reports

April 27-28, 2010

Europe

 

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Qualification & Validation of Facilities and Utilities

April 28-29, 2010

Montreal -Canada

 

 

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HPLC Method Development & Validation Procedures
for Pharmaceutical, Biotech and Medical Device Industries & Compliance Issues

April 28-29, 2010

Montreal, Canada

 

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Quality by Design

April 28-29, 2010

Europe

 

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FDA Pre-Approval Inspections

April 28-29, 2010

Montreal, Canada

 

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Preparing & Implementing an Effective
Change Control System

TBA

Philadelphia, USA

 

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Technology Transfer Planning
Planning and Management Strategies for a Successful Transfer
for Pharmaceutical, Biopharmaceuticals, and Biotech

TBA

Toronto, Canada

 

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Global Regulatory Submissions Process

TBA

 

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Third Party Audit & Supplier Qualification

May 4-5, 2010

Philadelphia, PA

 

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Lyophilization Technology & System Management

May 4-5, 2010

Philadelphia, PA

 

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Cleaning Validation Practices

May 4-5, 2010

Montreal, Canada

 

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Designing Pharmaceutical GMP Facilities

May 5-6, 2010

Montreal, Canada

 

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Quality by Design

May 5-6, 2010

Montreal, Canada

 

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Fundamental Tools in Statistics for GMP Compliance

A Two-Day Case Studies & Workshops for Life Sciences Professionals

May 10-11, 2010

Prague, Czech Republic

 

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Investigating Out-of-Specification (OOS) Results

for Pharmaceutical, Biotechnology, Medical Devices and Allied Industries

May 10-11, 2010

Czech Republic

 

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Developing an Effective Complaint Handling and Recalls Program

May 12-13, 2010

New Jersey, USA

 

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Analyzing Biological Assays

Computation, Validation, Acceptance & Troubleshooting

May 12-13, 2010

Toronto, Canada

 

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Pharmaceutical Impurities

Addressing US, European and ICH Requirements for Impurities; Strategies for Testing, Identifying and Controlling Impurities in Pharmaceuticals

May 12-13, 2010

Toronto, Canada

 

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Outsourcing Manufacturing and Partnerships with CMOs

Management Strategies to Develop Quality Partnerships in Pharmaceutical, Biopharmaceutical and Biotech Industries

May 12-13, 2010

New Jersey, USA

 

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Good Monitoring Practices for Medical Devices

May 18-19, 2010

Washington DC, USA

 

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Residual Solvents Testing

May 18-19, 2010

Philadelphia, USA

 

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Generic Drug Submissions & Approval

Preparing for Legal and Regulatory Requirements

May 19-20, 2010

Montreal, Canada

 

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Solid Dosage Production in cGMP Manufacturing

Principles, Practices and Strategies

May 19 – 20, 2010

Jersey City, USA

 

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Productivity, Quality and Continuous Improvement with Lean Six Sigma

May 19-20, 2010

Montreal, Canada

 

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Computer Systems Validation

May 25-26, 2010

United Kingdom

 

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Dissolution Testing in Pharmaceutical Analysis

May 25 – 26, 2010

Miami, FL - USA

 

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Technology Transfer Planning

Planning and Management Strategies for a Successful Transfer for Pharmaceutical, Biopharmaceutical and Biotech

May 26-27, 2010

New Jersey, USA

 

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Design, Development, and Implementation of a Validation Master Plan (VMP)

Best Practices for Managing Validation Activities

May 26-27, 2010

New Jersey, USA

 

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Cold Chain Management

May 26-27, 2010

United Kingdom

 

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European Filing & Registration

May 26-27, 2010

Europe

 

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Cleanroom & Contamination Control

June 1-2, 2010

Montreal, Canada

 

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Microbiological Food Safety Management

June 1-2, 2010

Montreal, Canada

 

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Analytical Instrument & Equipment Qualification

June 2-3, 2010

New Jersey, USA

 

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Process Analytical Technology

June 2-3, 2010

New Jersey, USA

 

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Computer Systems Validation

June 8-9, 2010

Philadelphia, USA

 

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Regulatory Strategies for Natural Health Products

June 8-9, 2010

Philadelphia, USA

 

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Effective SOP Development and Documentation Management

June 9-10, 2010

Montreal, Canada

 

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Biologics Comparability

June 9-10, 2010

Montreal, Canada

 

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Cleaning Validation Practices

For Pharmaceuticals & Biotech Industries Production

June 15-16, 2010

Czech Republic

 

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Preparing & Implementing an Effective Change Control System

June 15-16, 2010

Czech Republic

 

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Analyzing Biological Assays

Computation, Validation, Acceptance & Troubleshooting

June 16-17, 2010

Czech Republic

 

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How to prepare for System Based Inspection

June 16-17, 2010

Europe

 

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Implementation of Effective & Compliant CAPA Programs

Workshops, Case Studies & Interactive Exercises
Corrective and Preventive Action (CAPA) management is vital to an organization's regulatory compliance initiatives

June 23-24, 2010

Toronto, Canada

 

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Effective Process Validation

June 23-24, 2010

Toronto, Canada

 

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Packaging and Labelling

June 23-24, 2010

Toronto, Canada

 

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Cold Chain Management

For Pharmaceuticals & Biotech Industries Production

June 29-30, 2010

Philadelphia, USA

 

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Cleaning Validation Practices

For Pharmaceuticals & Biotech Industries Production

June 29-30, 2010

Philadelphia, USA

 

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Residual Solvents Testing: How to Apply USP <467>

Addressing US, European and ICH Requirements for Impurities;
Strategies for Testing, Identifying and Controlling Impurities in Pharmaceuticals

June 29-30, 2010

Philadelphia, USA

 

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Preparing & Implementing an Effective Change Control System

June 29-30, 2010

Montreal, Canada

 

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Preparation and Submission of Drug Master Files (DMFs)

Strategy for Meeting Your Regulatory and Processing Responsibilities

June 29-30, 2010

Montreal, Canada

 

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Dissolution Testing in Pharmaceutical Analysis

July 14 – 15, 2010

Budapest, Hungary

 

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Solid Dosage Production in cGMP Manufacturing

July 20 – 21, 2010

Calgary, Alberta

 

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GMP 2010

Sept 28-29, 2010

Toronto - Canada

A Two-day Can't Be Missed Conference, Workshops, and Exhibition.......

Combining Laboratory GMPs, Inspectional Issues, Method Development, Validation, and Stability Testing

 

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Lab Expo - The Greatest Laboratory Event of 2010

Oct 20-21, 2010

Toronto - Canada

A Two-day Can't Be Missed Conference, Workshops, and Exhibition.......

Combining Laboratory GMPs, Inspectional Issues, Method Development, Validation, and Stability Testing

 

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Cold Chain Management

TBA

Canada

 

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