Preparation and Submission of

Drug Master Files (DMFs)

Strategy for Meeting Your Regulatory and Processing Responsibilities

February 28-29, 2012

Jersey City, NJ - USA

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The Basics: Generation, Execution and Summary of IQ/OQ and PQ Protocols

March 6-7, 2012

Toronto, Canada

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Natural Health Product or Food:

How to Establish your Niche and Maximize Your Market Advantage

March 6-7, 2012

Ottawa, Canada

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Introductory Program:

Complying with GMP and cGMP Requirements -

Streamlining Quality Assurance & FDA Compliance

March 6-7, 2012

New Jersey, USA

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Mini Business Administration Training

March 7-8, 2012
March 27-29, 2012

Toronto-Canada

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6th Annual GMP-Update 2012 Conference

March 18-20, 2012

Dubai, UAE

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Common Technical Document (CTD) from Design to Submission

March 18-20, 2012

Cairo, Egypt

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What You Need To Control Your Production and Laboratory Processes

For the Pharmaceutical, Pivotal Clinical Manufacturing, Biologics and Medical Device Environment

March 20, 2012

Montréal, Canada

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Clinical Trial Process; ICH GCP, Clinical Trial Phases 0-4, Protocols, Informed Consent, Investigator Brochure

March 27-28, 2012

Montréal, Canada

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Training Course on How to Prepare for a Regulatory Audit

April 18-19, 2012

Philadelphia, PA, USA

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IPA's 6th Annual Cold Chain & Logistics Management

April 24-26, 2012

Orlando, Florida

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Quality By Design:

A Systematic Approach to Pharmaceutical Development, Approval and Manufacturing

May 16-17, 2012

Montréal, Canada

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Self Inspection and its Potential Benefits Via ICH Q9

May 16, 2012

Toronto, Canada

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Stability Testing Conference

May 16-17, 2012

New Jersey, USA

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Microbiology in Quality Control Laboratories

- To be announced -

Washington, DC

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