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Introduction to Sterile Produce Manufacture for those with a cGMP basic understanding (2 day)

 
  October 17, 2012  
     
 
PharmaTraining Limited, Window Conference Venue, 13 Windsor Street, Islington, London, N1 8QG
3 & 4 December 2012


Course Programme:
Day One (9am – 5pm)
Background:
• What is a sterile product?
• Classification of products.
• Why are they sterile?
Basic microbiology. The Regulatory environment.
• cGMP
• Facilities and processing.
• The impact of personnel and materials
• Environmental Monitoring.
• What is the difference and the impact or viable and non-viable
contaminants.
Day Two (9am – 5pm)
• Dosage Forms: syringes, ampoules, vials and others
• Sterilisation: Overview of methods of sterilisation, autoclave, dry heat
oven, radiation, filtration and EtOH exposure.
• Aseptic vs. Terminally sterilized, how do you decide?
• Areas of specialization. Where do I go from here?
 
 
Organized by: PharmaTraining Ltd
Invited Speakers: Paul Cummings
Paul is a Chartered Biologist, a Fellow Member of the Society of Biology and has
nearly 30 years experience in the Pharmacy/Pharmaceutical Industry and left GSK in
2009 to pursue a career as an Independent Consultant.
 
Deadline for Abstracts: .
 
Registration:

Discounted rate for registering and paying before 3 October 2012
- 2 day course £1062.00 (+ VAT if applicable, see VAT NOTES)

Discount of 10% applies for booking 8 weeks in advance. Discount of 10% applies
for booking more than 1 delegate. Discount of 10% applies for booking more than
1 course. Maximum discount received is 15%

E-mail: judy@pharma-training-courses.com
 
   
 
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