• Panithi is a graduate of the Faculty of Pharmaceutical, Chulalongkorn University and continued his graduate studies in synthetic chemistry. He holds a Ph.D. in Human Toxicology from the University of Iowa. Before Baiya Phytopharm, Panithi held various positions in pharmaceutical production at V.S. Pharma, Biopharma, and Mega Life Sciences.

• As regulatory affairs, Panithi is responsible for ensuring that our products meet regulatory standards and compliance requirements set by government agencies such as the Food and Drug Administration (FDA). He is responsible for obtaining regulatory approval for new drug formulations, and working on the regulatory aspects of developing and manufacturing biological products.

• Panithi has strong analytical skills, these are crucial for understanding of scientific principles, regulations and assessing their impact on product development and marketing strategies, interpreting complex regulations and an ability to communicate complex information effectively. He serves as the bridge between scientific research, legal compliance, and public safety work closely with research and development teams, providing scientific expertise to support product development and clinical trials with his ability to communicate.

Achievement: Panithi accomplished in the preparation of regulatory dossiers, coordinated with various departments, including clinical research, legal affairs, quality assurance, production, and research and development to organize regulatory information, data, documents, and other information. This collaborative effort resulted in successfully submitted regulatory filings within specified timelines to support clinical trials activities.

Panithi Saktrakulkla, PhD
Regulatory Affairs Manager

• Panithi is a graduate of the Faculty of Pharmaceutical, Chulalongkorn University and continued his graduate studies in synthetic chemistry. He holds a Ph.D. in Human Toxicology from the University of Iowa. Before Baiya Phytopharm, Panithi held various positions in pharmaceutical production at V.S. Pharma, Biopharma, and Mega Life Sciences.

• As regulatory affairs, Panithi is responsible for ensuring that our products meet regulatory standards and compliance requirements set by government agencies such as the Food and Drug Administration (FDA). He is responsible for obtaining regulatory approval for new drug formulations, and working on the regulatory aspects of developing and manufacturing biological products.

• Panithi has strong analytical skills, these are crucial for understanding of scientific principles, regulations and assessing their impact on product development and marketing strategies, interpreting complex regulations and an ability to communicate complex information effectively. He serves as the bridge between scientific research, legal compliance, and public safety work closely with research and development teams, providing scientific expertise to support product development and clinical trials with his ability to communicate.

Achievement: Panithi accomplished in the preparation of regulatory dossiers, coordinated with various departments, including clinical research, legal affairs, quality assurance, production, and research and development to organize regulatory information, data, documents, and other information. This collaborative effort resulted in successfully submitted regulatory filings within specified timelines to support clinical trials activities.