| Register for the Process Analytical Technology (PAT) Pharmaceutical Outsourcing Webinar... |
Process Analytical Technologies (PAT) is a communication tool that can reduce miscommunication that occurs during the transfer of a process to a partner for further development or manufacturing. Effective PAT provides quantitative measurements of the critical process variables that directly relate to batch success or failure. By monitoring the batch process in real-time, operators can better ensure that desired batch results are achieved - faster, more repeatable, and with tighter product quality.
As they implement Quality by Design (QbD) guidelines, pharmaceutical companies are becoming more dependent on PAT tools to improve internal communication throughout chemical and product development and manufacturing. PAT-related data is proving an effective language with which to document and communicate process guidelines and ensure product requirements - between sites and across borders.
As bio-pharmaceutical outsourcing suppliers search for ways to differentiate themselves and improve the efficiency of their own operations, the ability to communicate with the sponsor company in the language of standard PAT methods may prove to be a valuable next step.
Pharmaceutical Outsourcing Webinar Details
During this webinar, the application of Process Analytical Technologies to improve outsourcing communication will be discussed. Specific case studies will be presented:
- Drug Product Manufacturing - Real-time batch control of high-shear wet granulation using in-process particle monitoring
- Process Safety - Standardized thermal analysis using reaction calorimetry to ensure safe process scale-up
- Active Pharmaceutical Ingredient (API) Manufacturing - In situ reaction monitoring to ensure batch consistency between outsourcing partners
- Crystallization - Using PAT monitoring of batch crystallization to simplify tech transfer between sites
Webinar Presenter
Your online presenter, Terry Paul Redman, has over 12 years of experience helping pharmaceutical companies and their partners successfully implement PAT technologies for improved understanding and direct control of critical process parameters in a variety of processes including API synthesis, crystallization, and product formulations.
Interactive
At the end of this online seminar, there will be an interactive Q&A session providing you with the opportunity to ask questions.
1 Shadle, Paula J., Outsourcing GMP manufacturing of drugs and biologies, Speciality Chemicals Magazine, May 2008, pp. 14-15
As part of the METTLER TOLEDO commitment to continuing education for Contract Manufacturing Organizations (CMOs) and bio-pharmaceutical companies, we offer complimentary educational webinars that explore the industry and application information relevant to Chemists and Chemical Engineers.