Forced Degradation Studies/ Biologics Stability Programs for Biopharmaceuticals

Speaker

Instructor: Nanda Subbarao
Product ID: 701748

Location
  • Duration: 90 Min
This 90-minute training will provide you with an overview of a forced degradation study on a protein therapeutic and help you interpret and leverage the results to design stability studies required for registration of the BLA.
Purchase option for this webinar is currently unavailable. Please contact our Customer Care for more info.

 

Customer Care

Fax: +1-650-362-2367

Email: [email protected]

Read Frequently Asked Questions

Why Should You Attend:

A comprehensive forced degradation study is essential for design of an analytical program which when implemented right from the initial stages of a project will result in right-first-time CMC data package and therefore lead to cost savings in terms of analytical lab and regulatory department resource requirements. The forced degradation results must be incorporated in the design of the compliant stability program which is essential for the success of a well characterized protein product.

This 90 minute session is designed to provide the attendee with an overview of a forced degradation study on a protein therapeutic and to interpret and leverage the results to design the stability studies required for registration of the BLA. The speaker will address the stress conditions typically used to study the tendency of the protein to undergo degradation along with the analytical methods required for the study. Forced degradation study data must be utilized during the design of the stability program. We will discuss how you can leverage the forced degradation results to design stability studies for the drug substance and drug product. The regulatory requirements for such studies will be addressed.

Areas Covered in the Webinar:

  • What is the purpose of a forced degradation study?
  • What are the conditions to be used during well characterized protein forced degradation study?
  • How to test for the degradants?
  • Design of a compliance wcp stability study based on the forced degradation results.
  • How to conduct a biologics stability study?
  • Common mistakes during forced degradation studies

Who Will Benefit:

  • Stability department personnel
  • R&D laboratory personnel
  • R&D laboratory supervisors and management
  • QC laboratory personnel and management
  • Protein formulation group personnel and management
  • Regulatory affairs personnel
  • Regulatory affairs management
Instructor Profile:
Nanda Subbarao

Nanda Subbarao
Senior Consultant, Biologics Consulting Group

Dr. Nanda Subbarao holds a Ph.D. in Bio-organic Chemistry. Her hands-on industrial experience covers stability and laboratory cGMP systems for both biologics and conventional drugs. She has extensive experience in evaluation of analytical methods and method validation for products ranging from conventional drugs, well characterized proteins, vaccines, cell therapy and gene therapy products, ranging from pre-clinical phase to commercial phases. She has extensive expertise in setup of cGMP/GLP complaint quality systems for laboratory and stability programs as well as upgrade of existing quality systems for products during development and in commercial phases. She is currently a senior consultant with the Biologics Consulting Group specializing in analytical, stability, CMC and GLP/GMP quality systems. She serves on the AAPS Stability Focus Group Steering Committee as well.

Follow us :

 

 

Refund Policy

Our refund policy is governed by individual products and services refund policy mentioned against each of offerings. However in absence of specific refund policy of an offering below refund policy will be effective.
Registrants may cancel up to two working days prior to the course start date and will receive a letter of credit to be used towards a future course up to one year from date of issuance. ComplianceOnline would process/provide refund if the Live Webinar has been cancelled. The attendee could choose between the recorded version of the webinar or refund for any cancelled webinar. Refunds will not be given to participants who do not show up for the webinar. On-Demand Recordings can be requested in exchange. Webinar may be cancelled due to lack of enrolment or unavoidable factors. Registrants will be notified 24hours in advance if a cancellation occurs. Substitutions can happen any time. On-Demand Recording purchases will not be refunded as it is available for immediate streaming. However if you are not able to view the webinar or you have any concern about the content of the webinar please contact us at below email or by call mentioning your feedback for resolution of the matter. We respect feedback/opinions of our customers which enables us to improve our products and services. To contact us please email [email protected] call +1-888-717-2436 (Toll Free).

 

 

+1-888-717-2436

6201 America Center Drive Suite 240, San Jose, CA 95002, USA

Follow Us

facebook twitter linkedin youtube

 

Copyright © 2021 ComplianceOnline.com MetricStream
Our Policies: Terms of use | Privacy

PAYMENT METHOD: 100% Secure Transaction

payment method