IPA Past Events

	Process Validation Workshops August 17 - 18, 2010 Montreal - Canada
	The International API GMP Guidance: ICH Q7 Implementation and Application August 17-18, 2010 Montreal, Canada
	Solid Dosage Production in cGMP Manufacturing July 20 – 21, 2010 Calgary, Alberta
	Cleaning Validation Practices & Critical Cleaning Processes For Pharmaceuticals & Biotech Industries Addressing the Most Current Requirements & Practices for Effective Cleaning Validation June 22-23, 2010 Somerset - NJ, USA
	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 15-16, 2010 Boston, MA - USA
	Best Practices for science and compliance in Pharmaceutical Microbiology Workshops, Case Studies & Interactive Exercises June 15-16, 2010 Boston, MA - USA
	Introduction to Regression and Design of Experiments June 15-16, 2010 Boston, USA
	Quality Risk Management June 8-9, 2010 Montreal - Canada
	What to expect and how to prepare for FDA Inspection Understanding the Current FDA Positioning and ensuring Compliance May 26-27, 2010 Montreal, Canada
	Residual Solvents Testing: How to Apply USP <467> Interpreting and Implementing ICH Q3C Requirements Strategies to meet new USP residual solvent requirements May 19-20, 2010 Somerset, NJ - USA
	Qualification & Validation of Facilities and Utilities April 28-29, 2010 Montreal -Canada
	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
	GMP Chapter Effective Quality Assurance Auditing April 14-15, 2010 Montreal, Canada
	GMP Update On: Dietary Supplements & Natural Health Products April 21-22, 2010 Montreal, Canada
	Pharmaceutical Microbiology & Best Practices Addressing the most pressing issues in pharmaceutical microbiology April 7-8, 2010 Toronto, Canada
	New addition to Health Canada’s GMP regulation Annual Product Quality Review (APQR) and Annual Product Review (APR) March 24-25, 2010 Toronto, Canada
	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
	The CTD and eCTD Formats for NDA & BLA Submissions March 23-24, 2010 Philadelphia, USA
	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.
	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
	Process Validation for the 21st Century for Biological and pharmaceutical March 30-31 2010 Philadelphia, USA
	4th Pharmaceutical & Biotech GMP Conference February 21-23, 2010 Dubai, United Arab Emirates
	Drug Master Files (DMFs) February 23-24, 2010 Somerset, NJ, USA
	Solid Dosage Production in cGMP Manufacturing Principles, Practices and Strategies February 24-25, 2010 Montreal, Canada
	Refresher Training Course on GMP regulations and guidelines February 25-26, 2010 Montreal, Canada Build Excellence & Strengthen your Workforce Refresh your Good Manufacturing Practice (GMP) awareness in manufacturing and packaging.
	Fundamental Tools in Statistics for GMP Compliance February 2-3, 2010 Greater New York City Area, USA A Two-day Case Studies & Workshops for Life Sciences Professionals
	Drug Products Stability and Shelf-Life January 26-27, 2010 Dallas, TX - USA
	New addition to Canadian GMP regulation Annual Product Quality Review (APQR) and Annual Product Review (APR) December 3-4, 2009 Montreal, Canada Strategy for putting together a comprehensive and compliant Annual Product Quality Review (AQPR) report
	Microbiology Testing in Pharmaceutical Industry December 3-4, 2009 Montreal, Quebec, Canada
	Cold Chain Management 2009 November 19-20, 2009 Montreal, Quebec, Canada
	Refresher Training Course on GMP regulations and guidelines November 19-20, 2009 Toronto, Canada Build Excellence & Strengthen your Workforce Refresh your Good Manufacturing Practice (GMP) awareness in manufacturing and packaging.
	Drug Products Stability and Shelf-Life November 19-20, 2009 Prague, Czech Republic This one and half day course and workshop is designed to provide everything you need to know on how to design and implement a comprehensive and compliant stability program.
	Best Practices for Conducting Forced Degradation Studies November 17, 2009 Greater New York City Area, USA
	Statistical Tools and Analysis for GMP Compliance October 29-30, 2009 Toronto, Canada Strategy and techniques on how to conduct effective statistical analysis and reporting by providing an overview of statistical tools and methods in a GMP compliance environment.
	Conducting Effective Out-Of-Specification (OOS) Investigations October 19-20, 2009 Somerset, New Jersey-USA Investigation Techniques and Strategies to meet Regulatory Scrutiny
	Quality by Design October 19-20, 2009 Somerset, NJ - USA Challenges of implementing QbD / PAT in the development of rugged and robust formulations, processes, and Approvals Making QbD real and cost effective for both R&D and Manufacturing
	Effective Process Validation October 1-2, 2009 Montreal, Canada 2-day course and interactive workshops on Developing a Robust Strategy for Implementing Key Requirements & Best Practices for Process Validation
	GMP UPDATE 2009 September 24-25, 2009 Montreal, Canada Global Perspectives for Pharmaceutical, Biopharmaceutical and Allied Industries. The greatest gathering of GMP experts from across the globe addressing the current challenges of GMPs With participation from: Health Canada, MHRA, WHO and ...
	Effective Quality Assurance Auditing September 17-18, 2009 New Jersey, USA
	Root Cause Analysis (RCA) & Corrective and Preventive Action (CAPA) August 20-21, 2009 Montreal, Canada
	Drug Products Stability and Shelf-Life August 20-21, 2009 Toronto, Canada This one and half day course and workshop is designed to provide everything you need to know on how to design and implement a comprehensive and compliant stability program.
	Environmental Monitoring Program August 20, 2009 Montreal, Quebec - Canada
	Leadership Workshop August 17-18, 2009 Toronto, Canada
	Critical Documentation Control for Laboratory Operations August 10-11, 2009 Toronto, Canada
	Aseptic Processing Operations in the Manufacture of Biotech and Pharmaceutical Products June 22-23, 2009 Montreal - Canada
	Residual Solvents Testing: How to Apply USP <467> June 22-23, 2009 Montreal - Canada
	Regulatory Strategies for Natural Health Products June 15-16, 2009 Montreal - Canada
	Drug Products Stability and Shelf-Life May 28th - 29th, 2009 Boston, USA This one and half day course and workshop is designed to provide everything you need to know on how to design and implement a comprehensive and compliant stability program.
	Preparation and Submission of Drug Master Files (DMFs) May 28 -29, 2009 Boston, MA Strategy for Meeting Your Regulatory and Processing Responsibilities
	Computer System Validation May 28, 2009 Montreal, QC - Canada What Computer System Validation is and how it saves your company money
	Refresher Training Course on GMP regulations and guidelines April 28-29, 2009 Somerset, New Jersey - USA Build Excellence & Strengthen your Workforce Refresh your Good Manufacturing Practice (GMP) awareness in manufacturing and packaging.
	Computer Systems Validation April 28-29, 2009 Somerset, New Jersey - USA Keeping up to date with new technological developments and managing change. Strategy for Simplifying the Computer Systems Validation Process to Maximize Compliance and Reduce; cost, effort, time, and documentation.
	Quality By Design April 27th-28th, 2009 Toronto - Canada A Comprehensive and Systematic Approach to Development and Manufacturing. With participation from Abbott Laboratories, Eli Lilly and Company, Novartis Pharmaceuticals Corp., Schering-Plough Research Institute, Epcot International, Umetrics Inc. and Wyeth.
	Pharmaceutical Packaging & Labeling April 2nd - 3rd, 2009 Montreal, Canada Best Practices for Regulatory Compliance and Innovation. With participation from Health Canada, Alcan, Cameo Crafts, Health Compliance Packaging Council, Packaging Science Resources,
	Facility Design, Qualification, and Validation of Pharmaceutical and Biotech Manufacturing Sites April 2nd - 3rd, 2009 Montreal, Canada
	Cleaning Validation Practices March 30th-31st, 2009 North Carolina, USA This course has been designed to provide practical advice on how to design and execute cleaning validation studies to meet current regulatory expectations in a cost-effective way. With participation from Dober Research Works, Hall & Pharmaceutical Associates, Inc., Alconox, Sani Matic, Steris, ITW Texwipe and PharmaSys.
	Pharmaceutical Impurities March 30th-31st, 2009 Somerset, New Jersey - USA Addressing US, European and ICH Requirements for impurities Strategies for Testing, Identifying and Controlling Impurities in Pharmaceuticals. New Addition to the Program - Application of LC-MSn in the Elucidation of Drug Degradation Products
	Preparing & Implementing an Effective Change Control System March 26th-27th, 2009 Toronto - Canada A Two Day Comprehensive & Interactive Course with Workshops and Case Study Discussion. With participation from Quality & Compliance Associates and VelQuest Corporation.
	Conducting Effective Out-Of-Specifications (OOS) Investigations December 11th-12th, 2008 Montreal, Canada With participation from CQI Consulting Ltd., The Quantic Group and Parexel Consulting
	Natural Health Products & Dietary Supplements December 4th-5th, 2008 Toronto, Canada With participation from Health Canada, U.S. Pharmacopeia, Jamieson Laboratories, NSF International, CHFA, Canreg, ndmac, Nutralab, Silliker, Cassels, dsa conultants and Dr. A.W. Matin.
	Drug Products Stability and Shelf-Life December 4th-5th, 2008 San Francisco, USA A One & Half Day Comprehensive & Interactive Course with Case Studies & Workshops. With Participation from QCL-Quality Compliance Laboratories
	Biosimilars December 4th-5th, 2008 Toronto, Canada With Participation From Health Canada, Alba Biologics, analiza, Amgen, Bereskin & Parr, McDermott will & Emery, Microbix, Torys LLP, Parexel Consulting and Sartorius Stedim Biotech..
	Transportation and Distribution Management of Temperature November 17th-19th, 2008 Montreal, Canada With Participation from Health Canada, Abbott, Wyeth, FedEx Custom Critical, IATA, ThermoSafe, Toronto Pearson, Sensitech, ATS Healthcare Soluations, Exelsius, Veriteq, Sentry, Drumbeat Dimensions, Inc., Evidencia, WEI and dsa consultants
	3rd cGMP Update 2008 November 16th-18th, 2008 Dubai, UAE The greatest gathering of GMP and Validation experts addressing the most pressing issues and best practices to ensure Global Regulatory Compliance.
	GMP UPDATE 2008 October 20th-21st, 2008 Toronto, Canada Meeting the Emerging Global Compliance Challenge. With Participation From Health Canada, MHRA, WHO, Former FDA, AAI Pharma, Former Health Canada, Canreg, Pharmatech, IPEA, Pfizer, Medidata, Jamieson, and Torys LLP.
	Conducting Internal Audits October 2nd - 3rd, 2008 Montreal, Canada With participation from Diosynth Biotechnology, Compliance Gurus and Quality Support Group, Inc.
	Microbiology Best Laboratory Practices October 1st-3rd, 2008 Montreal, Canada With participation from Former Health Canada, AAI Pharma, Advanced Barrier, EMD, Human Genome Sciences, MedImmune and MEI
	Implementing HACCP Program and Quality Risk Management September 29th-30th, 2008 Toronto, Canada With Participation From Quality Medical Regulations Services, The Weinberg Group and Medical HACCP Alliance.