A3P - Association pour les produits propres et stériles - Organisation d'évènements scientifiques

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A3P congress atmosphere (widescreen)

But where are our seniors? by Dominique Sierakowski, administrator A3P

In the mood or humor? You choose. Before you go looking for our seniors, I propose to try to specify that you want to talk, in other words: What a senior in 2010?

During a Biarritz congress

Indeed you already have the program for 22nd international A3P Congress of Biarritz, but you also have to spare your time of the best way to have the feeling to have made a success of your stay. I had received this wise advice of a former colleague whe

Thursday, September 2nd 2010

Gert Moelgaard

Lean Approach to Implementation of ASTM E2500 principles

	Are your information technology (IT) systems at risk? Computerized systems are subject to constant attention from the pharmaceutical companies that have, for the most part, developed a policy and appropriate procedures in the selection
Monday, May 3rd 2010

	The compatibility of materials with industrial technologies of sterilization There are several methods of sterilization of medical devices. The most common are the steam (or autoclave), ionizing radiations and ethylene oxide.
Tuesday, June 16th 2009

	Lean Validation Lean approaches in validation are nothing new in our industry, methods in ‘streamlining (as it used to be termed)’ have been around since the early ‘90s and conceptualised in trade publications as early as the late ‘80s.
Monday, July 27th 2009

	Printing labels Printing labels for pharmaceutical industry require a production process with no-fault quality insurance moreover when labels are dedicated for injection drugs.
Monday, August 31st 2009

	What technology for controlling the package? The new regulations and the effectiveness of pharmacovigilance put pressure on pharmaceutical packaging, leading to the proliferation of checkpoints on the packaging lines...
Tuesday, June 16th 2009

	How instantaneous microbial can be used by pharmaceutical manufacturer The instrument, IMD, has the capability of detecting the presence of bacteria and fungi in the environmental air. Its intended application is for environmental monitoring in a pharmaceutical facility.
Sunday, July 18th 2010

	Are you able to guarantee the validity of the tests on your production environment? One of the fundamental criteria of quality products is clean and sterile particulate and microbiological purity. The latter depends directly on the control of environmental conditions of their manufacture.
Monday, April 19th 2010

	Sterilizing filtration Is there a negative impact on the bioburden related to the use of non aseptic pre-filtration devices?
Tuesday, June 29th 2010

	Standard ISO 15378 Primary packaging materials for medicinal products Good Manufacturing Practices (GMP) require that manufacturers can demonstrate and verify the on-going compliance of their suppliers.
Monday, June 21st 2010

	Qualification of high sensitivity ATP-metry for the monitoring of ultra-pure water The microelectronic and pharmaceutical industries use ultra-pure water (UPW) in their production process. Bacterial contamination of this type of water (1,2) is cause of defects and costly non-quality consequences.
Tuesday, April 6th 2010