Select a Location
Asia
Australasia
Europe
Middle East
North America
South America
All Regions
Login
Pharma IQ
About Pharma IQ
Membership
All Upcoming Events
CD ROM & Documentation
Opportunities
Sponsorship & Exhibitions
Speaking
Marketing
Company Information
Company Profile
Careers With IQPC
Contact Us
Privacy Policy
Cancellation Policy
Webcasts
Meeting Canadian Regulatory and Inspection Requirements for Temperature Sensitive Products
• Understanding the feedback from recent audits on how to show evidence of compliance: Are you conducting the right validation studies for -20°F?
• Describing stability studies and data that work
• Recognizing how manufacturers can assist the Canadian Provinces when there is a cold chain breach
Harold Rode, Chief, Pandemic Influenza Division, Biologics and Genetic Therapies Directorate, Health Canada
MHRA Regulatory Feedback - Ensuring Your Products Comply With European Temperature Control Regulations From Clinical Materials to Marketed Products
• Comparing MHRA regulations with other European National Agencies – Are U.S. companies on the right track to comply across Europe?
• Gaining a European regulatory view on how industries can gain more control of temperature-sensitive products further downstream in the cold chain
• Clinical materials – What are the Regulators concerns and expectations?
• Describing what information and how much should be included in quality reports and risk assessments
Ian Holloway, Manager, Defective Medicines Report Centre, MHRA
The Final Updated Revisions to General Chapter 1079: Practical Guidance to Updating Your Cold Chain Management
• Explaining recommended control strategies – from warehouse through end-user
• Describing specific protocols for receiving, shipping and storing – when, how and how much
• Following the tables in the updated guidance to make the right choices in your cold chain management
• Understanding the updated SOPs and how to implement them
Dr Mary Foster, USP Packaging and Storage Expert Committee Member, US Pharmacopeia (USP)
View All Webcasts
Upcoming Events
Filter By Region
North America
Australia/NZ
Europe
Reducing Toxicity in Drug Compounds
Reduce your failure rate in drug development by effective early stage toxicity modelling, prediction and testing
January 26 - 27, 2009 *
The Grosvenor Victoria, London, UK
Cool Chain Europe 2009
January 27 - 29, 2009 *
Sheraton Brussels Airport Hotel and Conference Centre, Brussels, Belgium
Polymorphism and Crystallisation 2009
Simplify Your Polymorph Screening and Crystal Growth Strategies to Ensure Effective Scale-Up
March 11 - 13, 2009 *
Thistle Marble Arch, London, UK
European Pharmaceutical Contract Manufacturing 2009
March 24 - 25, 2009 *
Venue to be confirmed, London, UK
Compound Management & Integrity 2009
May 18 - 20, 2009 *
Radisson Edwardian Heathrow, London, UK
View All Events
Top Events
2nd Enhanced Solubility & Bioavailibility
February 09 - 11, 2009 · Relexa Hotel, Frankfurt/Main, Germany
Industry News
BBC Monitoring Central Asia | Jan 6 2009 5:32AM
Tajik Police Seize Over 1.3 T of Drugs in 2008
Business Wire | Jan 6 2009 5:04AM
Research and Markets: Forecasts and Competitive Intelligence on Italy's Pharmaceuticals and Healthcare Industry for Q4 2008
The News & Observer | Jan 6 2009 4:50AM
BRIEF: PPD Buys Merck Vaccine-Testing Lab
Datamonitor | Jan 6 2009 2:22AM
Dor Wins FDA Clearance to Initiate Phase III Graft-Versus-Host Disease Study
PRNewswire-FirstCall | Jan 6 2009 1:31AM
ExonHit Therapeutics Expands Strategic Collaboration With Allergan
View All Industry News
Recommended Books
Pharma Books