Overview:
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 considered sterile.
Areas Covered in the
session:
- Regulations relating to sterilization of products
- Methods of
sterilization
- Why one method is used
over another
- Validations of the
sterilizations method
- Parametric release
Who will benefit:
This webinar will
provide valuable assistance to the following personnel in pharma, biopharma and
food manufacturing companies:
- Quality Assurance
- Quality Control
- Manufacturing
- Quality system
auditors
- Microbiology analysts
and technicians
- Consultants
- Regulatory and Compliance Management
Instruction:
Live attendees will receive a Webex meeting invitation upon successfully completing the registration.
Participants who have opted for recorded version of the program will receive a Webex link within 8 hours after completion of the event. Using the link you can view/download the event as many times as you want.
Carl Patterson is a seasoned Pharmaceutical Manufacturing, Aseptic Processing, and Quality Assurance Professional who is based in San Diego, California. As soon as he discovered the importance of biotechnology in the area, he was inspired to enter the pharmaceutical manufacturing industry. However, his avid interest in all things biology, microbiology, and biochemistry officially began when he served in the U.S. Army as a Preventative Medicine Specialist and a Licensed Vocational Nurse.
To date, Carl has now garnered over two decades’ worth of extensive hands-on expertise. Currently, he is the Chief Consultant of his very own consultant business called aseptic-process.net, where he specializes in the aseptic processing of pharmaceutical products in the pharmaceutical manufacturing sector. Recently, he is in the process of creating webinars so he can share pertinent information about pharmaceutical manufacturing from a microbiological perspective.
Furthermore, Carl holds various degrees and certifications, including an M.S. in Biomedical Quality Systems from San Diego State University, a B.S. in Microbiology from the University of Texas, and Specialized Certificates in QA/QC & Biotechnology from UCSD.
Enrollment Options
Tags: Sterilization of Pharmaceutical Products and Medical Devices, Carl Patterson, Webinar, Amorit Education