The healthcare industry has raised the quality standards to protect patients and consumers. Any discussion about quality is incomplete without talks of Process Analytical Technologies (PAT) and Quality by Design (QbD).
PAT & QbD focuses on building quality at the initial stages in contrast to the traditional method of policing quality in the final dosage form. Its adoption has increased manufacturing efficiency, enabled process control, increased assurance of consistent product quality and in the long run will make the process more cost-effective.
Read MoreIt is a long established fact that a reader will be distracted by the readable content.
It is a long established fact that a reader will be distracted by the readable content.
It is a long established fact that a reader will be distracted by the readable content.
Training by the industry pioneer for Quality by Design (QbD) and Process Analytical Technology (PAT) for Pharmaceuticals & Biopharmaceuticals.
Comprehensive understanding of PAT &QbD including current uses and promised use.
Comprehensive manual with examples and case studies for further education on the PAT &QbD process.
An understanding of the guidelines and regulatory expectations.
Enhance the skills and knowledge on DOE.
Gain insights on statistical tools and risk-based approach.
Tech-transfer and Continuous improvement Process Verification along with validation lifecycle approach.
Techniques for better industry – academia collaboration.
Learn strategies for successful implementation of PAT and QbD techniques in Continuous manufacturing and API processes.
