Mari Katada

Regulatory Affairs Specialist | Waukegan, Illinois, United States

Professional Overview

Mari Katada is a seasoned Regulatory Affairs Specialist with a strong track record of navigating complex regulatory landscapes to ensure product compliance and market access. Adept at interpreting regulations, developing strategic regulatory plans, and collaborating cross-functionally, Mari brings a wealth of industry expertise to her current role.

Experience Summary

Current Role

As a Regulatory Affairs Specialist at #, Mari is responsible for overseeing the registration and regulatory approval processes for a diverse portfolio of products. She works closely with cross-functional teams to ensure all submissions and documentation adhere to strict regulatory requirements, proactively identifying and mitigating potential compliance risks. Through her strategic guidance and meticulous attention to detail, Mari has played a pivotal role in securing successful market launches and maintaining ongoing product registrations.

Career Progression

Prior to her current role, Mari held positions of increasing responsibility within the regulatory affairs field. She began her career as a Regulatory Affairs Coordinator at a leading pharmaceutical company, where she gained invaluable experience in navigating global regulatory frameworks and streamlining submission processes. Mari's demonstrated success in this role led to a promotion to Regulatory Affairs Specialist, where she honed her expertise in regulatory strategy and stakeholder management.

Academic Background

Mari holds a Bachelor of Science degree in Pharmaceutical Sciences from the University of Illinois at Chicago, where she graduated with Honors. Her academic background provides a strong foundation in pharmaceutical regulations, quality assurance, and industry best practices.

Areas of Expertise

• Regulatory strategy and compliance

• Preparation and submission of regulatory dossiers

• Maintaining product registrations and market authorizations

• Cross-functional collaboration and stakeholder management

• Interpreting and applying relevant regulations and guidelines

Professional Impact

Throughout her career, Mari has been recognized for her contributions to successful product launches and her ability to navigate complex regulatory environments. She has played a pivotal role in several high-profile projects, ensuring timely regulatory approvals and facilitating the introduction of innovative products to the market. Mari's expertise and dedication have made her a valuable asset to her organization and a respected professional within the regulatory affairs community.

Conclusion

With her comprehensive industry knowledge, strategic thinking, and exceptional regulatory affairs capabilities, Mari Katada is poised to continue making significant contributions to her organization and the broader pharmaceutical industry. Her passion for compliance, coupled with a proven track record of successful regulatory submissions, positions her as a trusted advisor and a catalyst for driving organizational growth and innovation.