STERILIZATION OF PHARMACEUTICAL PRODUCTS AND MEDICAL DEVICES ( Recorded Event )

Posted By : User Ref No: WURUR70179 0
  • Image
  • TypeWebinar
  • Image
  • Location Dufferin, Ontario, Canada
  • Price
  • Date 19-11-2020 - 19-11-2021
STERILIZATION OF PHARMACEUTICAL PRODUCTS AND MEDICAL DEVICES ( Recorded Event ), Dufferin, Ontario, Canada
Webinar Title
STERILIZATION OF PHARMACEUTICAL PRODUCTS AND MEDICAL DEVICES ( Recorded Event )
Event Type
Webinar
Webinar Date
19-11-2020 to 19-11-2021
Location
Dufferin, Ontario, Canada
Organization Name / Organize By
Eventura World
Presented By
Carl Patterson
Sponsored By
Eventura World
Organizing/Related Departments
Training Department
Organization Type
Training/Development
WebinarCategory
Both (Technical & Non Technical)
WebinarLevel
All (State/Province/Region, National & International)
Related Industries

Education/Teaching/Training/Development

Research/Science

Biotechnology

Manufacturing

Medical/Healthcare/Hospital

Location
Dufferin, Ontario, Canada

Description

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.

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. There are four typical ways a product can be sterilized. These are sterilization by Ethylene Oxide, Gamma irradiation, Steam and Pressure, and filtration. Knowing the characteristics of your product will determine what method will be used. This webinar will go over the four methods of sterilization and why one method would be chosen over the other.

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 Should Attend:

  • Quality Assurance Departments
  • Quality Control Departments
  • Manufacturing Departments
  • Regulatory Departments
  • Compliance Departments
  • Quality system auditors
  • Microbiology analysts and technicians
  • Consultants

Others Details

Recorded Event

Registration Fees
Available
Registration Fees Details
Recording - Single $350.00 Recording - Corporate $1400.00
Registration Ways
Email
Phone
Website
Address/Venue
  Recorded Event 
Official Email ID
Contact
Komala

5939 Candlebrook Ct, Mississauga, ON L5V 2V5, Canada

[email protected]

     +1-416-915-4458