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.
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
"Teacher competent and available to give help and suggestions"
"For a 2 day course- all 2 days of info were of interest!!"
"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."
"Nadine Ritter is excellent!!"
"Ms Ritter was very well informed of the latest requirements (EU & US) and knowledgeable!"
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:
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Photostability
Stability Testing
Forced Degradation
Stress Testing
Brackating and matrixing

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