Events.
If Advanced Technology Products is hosting or attending any
industry events, notice will be posted in this section. We may also
choose to display events we believe will be of interest to our
clients.
 Preparing for a Regulatory Inspection.
Preparing for a Regulatory Inspection.
7-8th December 2006. RSSL Pharma Trainings Science & Technology Centre, University of Reading, Earley Gate, Whiteknights Road, Reading, Berkshire, UK.
Check our their website www.rssl.com
for more information.
Preparing for a Regulatory Inspection
Failure Investigation and Routine Cause Analysis.
Failure Investigation and Routine Cause Analysis.
4-5 December 2006. RSSL Pharma Trainings Science & Technology Centre, University of Reading, Earley Gate, Whiteknights Road, Reading, Berkshire, UK.
Check our their website www.rssl.com
for more information.
Failure Investigation and Routine Cause Analysis
Cleanroom Management.
Cleanroom Management for the Manufacture of Sterile Products.
23-24 November 2006. RSSL Pharma Trainings Science & Technology Centre, University of Reading, Earley Gate, Whiteknights Road, Reading, Berkshire, UK.
Cleanroom Management
Equipment Qualification and Method Validation.
Practical Equipment Qualification and Method Validation.
13-14th November 2006 at the RSSL Pharma Training, Science & Technology Centre, University of Reading, Earley Gate, Whiteknights Road, Reading, Berkshire, UK, RG6 6BZ.
Equipment Qualification and Method Validation
Cleanroom Test Methods Updated.
30th-November.Novotel Stevenage, United Kingdom.
Half- day seminar and table-top exhibition is directed at engineers and technicians involved in the design or validation of HEPA filtered enclosures and will review 3 current standards that are in the process of change.
Cleanroom Test Methods Updated
Critical Process and Cleaning Validation.
Critical Process and Cleaning Validation
Nov 29-1st December 2006.Radisson SAS St Helen's, Stillorgan Road, Dublin, Ireland.
Solid overview of the principles and technology of residue removal and residue measurement.
Cleaning Process and Cleaning Validation
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