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Carl Patterson

Carl Patterson, M.S. is Keynote Speaker at Compliance key Inc. He has completed twelve (12) plus years in the biotechnology, pharmaceutical manufacturing, and quality fields. He completed his Bachelor's of Science in Microbiology from the University of Texas. Also, has completed specialized certificates in biotechnology manufacturing, quality control, and quality assurance from UCSD, and has completed his Master's of Science in Biomedical Quality Systems from SDSU. Through the years, has worked with several companies in regards to aseptic processing and has helped to insure the expectations, related to aseptic processing, have been met. 

 
   
Live Webinars   Recorded Webinars
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LSHCSCP003
07/13/2017
10:00 AM PST | 01:00 PM EST,
Duration 60 mins
Carl Patterson  
Sterilization of Pharmaceutical Products and Medical Devices

This topic will discuss the methods of sterilization to be used on medical devices and pharmaceutical products. Understanding the regulations pertaining to sterilization of products will help to decide with method to use for your product. The advantages and disadvantages of each will be discussed. V....

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$165 
Single Live
(Only for one Participant)
$335 
Multiple Single
( 2 - 5 Participants)
$670 
Corporate Live
( 6 - 10 Participants)
$193 
  Recorded
(6 months unlimited access)
 
LSHCGCP002
Duration 60 mins
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recorded  
GMP Auditing for Pharmaceutical Manufacturing

Auditing involves a comprehensive review of vendors that will provide resources and/or services. The ICH Q10 document provides an outline on the pharmaceutical drug product life-cycle. Through the review of ICH Q8, Q9, and Q10, the participant will be able to audit the various activities associated....

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$193 Recorded (6 months unlimited access)
 
LSHCACP001
Duration 60 mins
View Anytime
recorded  
Auditing for Microbiological Aspects of Pharmaceutical and Biopharmaceutical Manufacturing

The seminar provides a comprehensive overview of auditing for microbiological aspects of pharmaceutical and biopharmaceutical manufacturing. The use of cleanrooms to manufacture drug products has been done for years. Microbiological aspects of manufacturing have been incorporated into the manufactur....

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$193 Recorded (6 months unlimited access)
 
LSHCCPA001
Duration 60 mins
View Anytime
recorded  
Environmental Monitoring - Knowing your Cleanroom

This webinar will provide the proper methods and techniques required to maintain a clean room per FDA and ISO regulations. By the use of viable and non-viable testing, a cleanroom can be maintained. The results collected can determine the state of control the cleanroom operates on a continuous bas....

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$193 Recorded (6 months unlimited access)
 
 
 
 

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