Nowadays, interaction between different pharmaceutical companies and CDMOs is more and more common. As a consequence, experts working in development and production departments are often faced with transferring a process or an analytical method from one laboratory/manufacturing site to another. Do you recognise these as some of the challenges you meet in your daily work? What are the do’s and don’ts? If you are struggling with these questions this training is certainly something for you/your department.
Protea will offer a 2.5 days on site course aimed at providing practical insights in the challenges of Technology Transfer. Focus will be among others on how implementation of Quality by Design principles is essential for a successful completion of the transfer and successive validation of a manufacturing process.The basic regulatory requirements will be also touched upon.
The course is meant to be interactive and there will be room for ample discussion. Case studies will be used to better understand the challenges of real life cases and how to overcome them.
Scope Provided by the Training:
- Understand industry current approaches for technology transfer;
- Get a valuable insight on the do’s and don’ts for successful technology transfer starting from real life example;
- Explore proven best practices for technology transfer of solid drug product formulations;
- Gain practical knowledge from interactive sessions and case studies;
- Take the opportunity to discuss issues and challenges.
Who Should Attend:
Any function involved in technology transfer activities.
This training can be tailored to the specific interests of your company. It has already been successfully delivered in house at Remedica Ltd and online at Symmetric.
