Reference standards are one of the key aspects in a Quality Control laboratory in the pharmaceutical industry. Correctly qualified reference materials are required to ensure valid QC results, which are the basis for a batch release by a QP. Because of this, the handling and usage of the correct standard is important.
Target Group
This webinar is designed for all persons working in Quality Control departments or contract laboratories. It will be of interest in particular for personnel from Quality Assurance departments as well as Auditors and Qualified Persons of pharmaceutical companies, suppliers and consultants.
Technical Requirements
For our webinars, we use Cisco WebEx, one of the leading suppliers of online meetings.
At http://www.webex.com/test-meeting.html you can check if your system meets the necessary requirements for the participation at a WebEx meeting and at the same time install the necessary plug-in. Please just enter your name and email address for the test. If the installation is not possible because of your rights for the computer system, please contact your IT department. WebEx is a standard nowadays and the necessary installation is fast and easy.
Programme
This webinar will give you a comprehensive overview of the GMP-compliant handling of reference standards. Regulatory requirements as well as the qualification and procurement of the reference standards will be discussed and explained.
Primary standards, Working standards, Ph. Eur. standards
Specific requirements and handling advices
How to handle Ph. Eur. standards in the daily business?
Testimonials