Medical Devices 2020 - Sterilization of Pharmaceutical Products and Medical Devices During COVID19 New Course
Topics/Call fo Papers
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.
Pharmaceutical products and medical devices are required to be sterile to be used in patients. Sterilization of these crucial products can be done in several ways depending on the characteristics of the product being sterilized.
Types of sterilization methods.
Predominant uses of sterilization within the Medical Device and Pharmaceutical/Biotech industries.
Product interactions with Various Modes of Sterilization.
When to Use one Sterilization Mode vs. Another.
Parametric Release – What is it?
Speaker:
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.
Pharmaceutical products and medical devices are required to be sterile to be used in patients. Sterilization of these crucial products can be done in several ways depending on the characteristics of the product being sterilized.
Types of sterilization methods.
Predominant uses of sterilization within the Medical Device and Pharmaceutical/Biotech industries.
Product interactions with Various Modes of Sterilization.
When to Use one Sterilization Mode vs. Another.
Parametric Release – What is it?
Speaker:
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.
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Last modified: 2020-10-16 23:46:33