Generic placeholder image

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. 

 Webinar Id: CKCP002
10:00 AM PT | 01:00 PM ET
 02/15/2018
 Duration 60 mins

Risk of Objectionable Microorganisms in Bio-Pharmaceutical Manufacturing

Objectionable microorganisms are considered,  if discovered, harmful to the patient. By identifying and controlling these microorganism and putting the appropriate controls place early in the pharmaceutical manufacturing or medical device manufacturing process problems in the patient can be prevented. This webinar will review the regulations pertaining to objectionable microorganisms, agency expectations, methods to identify objectionab........


View Details

               $ 179
       Single Attendee
(Only for one Participant)
         $ 363
Multiple Attendee
( 2 - 5 Participants)
          $ 726
Corporate Attendee
( 6 - 10 Participants)
                  $ 237
         Recorded
(6 months unlimited access)
 Webinar Id: LSHCGCP005
 View Anytime
 Duration 60 mins

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 with the different stages of the product lifecycle. By using a scientific risk-based approach, as outlined in ICH Q9, the participant will b........

$ 237  Recorded  (6 months unlimited access)

View Details

 Webinar Id: LSHCACP003
 View Anytime
 Duration 60 mins

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 manufacturing process. By understanding the microbiological aspect, auditors can understand whether the manufacturing facility is under control. There........

$ 237  Recorded  (6 months unlimited access)

View Details

 Webinar Id: LSHCSCP003
 View Anytime
 Duration 60 mins

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. Validation of each sterilization method will be discussed and how best to prove to a regulatory body the products being treated are considere........

$ 237  Recorded  (6 months unlimited access)

View Details

 Webinar Id: LSHCGCP002
 View Anytime
 Duration 60 mins

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 with the different stages of the product lifecycle. By using a scientific risk-based approach, as outlined in ICH Q9, the participant will b........

$ 237  Recorded  (6 months unlimited access)

View Details

 Webinar Id: LSHCACP001
 View Anytime
 Duration 60 mins

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 manufacturing process. By understanding the microbiological aspect, auditors can understand whether the manufacturing facility is under control. There........

$ 237  Recorded  (6 months unlimited access)

View Details

 Webinar Id: LSHCCPA001
 View Anytime
 Duration 60 mins

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 basis. In order to maintain a cleanroom, a proper cleaning agent rotation needs to be implemented. The webinar will provide a discussion of the m........

$ 237  Recorded  (6 months unlimited access)

View Details



    
Copyright © 2017 Compliance Key . All Rights Reserved. Back to Top