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CMC Analytical, Comparability and Stability Studies for Biotechnology Products

Course Objectives

This practical 2-day training course presents all of the regulatory, technical and quality elements necessary to produce successful analytical test methods, product reference standards, comparability studies and stability protocols for biotechnology products in the US and EU.

What Will You Learn?

  • Clarify the latest CMC regulatory requirements for biotech products to ensure successful marketing applications

  • Assess comparability and stability considerations for biotech product specification

  • Design and develop your biotech stability protocols by identifying the key practical details to address

  • Validate your stability testing methods appropriate for each phase of development

  • Identify which characteristics of a biotech product require analytical assessment

  • Follow the ICH, FDA and USP guidelines for analytical method validation

  • Identify and implement key considerations for biotechnology laboratory testing

Why you should attend

  • Create compliant stability protocols
  • Ensure EU and FDA regulatory compliance
  • Identify specifications for release

Reviews

"Teacher competent and available to give help and suggestions"
CMC Officer
Creabilis Therapeutics
"For a 2 day course- all 2 days of info were of interest!!"
Associate Director Project management/CMC
Morphotek
"Very easy to follow the presentation and the speaker. Good complete presentation. Very good resume of what is on the regulation texts and where it is."
Project Manager
Avogadro
"Nadine Ritter is excellent!!"
Director Analytical Outsourcing
Morphotek
"Ms Ritter was very well informed of the latest requirements (EU & US) and knowledgeable!"
Associate Director Project management/CMC
Morphotek

Who Should Attend

This training course is intended for the professional who is involved with stability testing for biotechnology products, directly or indirectly. Professionals from Pharmaceutical, Biotechnology, Drug Delivery and Medical Device companies should attend, such as, but not limited to:

  • Stability Directors/ Supervisors/Managers/Analysts/Coordinators
  • Laboratory Supervisors/ Managers
  • Project Managers/Coordinators
  • Quality Control Analytical Chemists
  • Research and Development Chemists
  • Biostatisticians
  • LIMS Administrators
  • QA/QC Reviewers
  • Validation Scientists
  • Calibration/Metrology Groups
  • Internal or Independent Auditors
  • Manufacturing/Production Managers

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Dates and Venues

14 Mar 2012 - 15 Mar 2012

MWB Victoria

24 Oct 2012 - 25 Oct 2012

MWB Victoria

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Key Topics Include...

Photostability

Stability Testing

Forced Degradation

Stress Testing

Brackating and matrixing

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Connect with the PTI faculty! PTI is a global pharmaceutical training company with over 60 interctive courses focusing on Regulatory Affairs, R&D, Clinical, Business Strategy, Fine Chemicals, Biopharmaceuticals, Manufacturing, Medical Devices and Agrochemicals 

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(updated 22 May 2012)


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