Britnee Ochabski

Britnee Ochabski is a Senior Clinical Research Associate (CRA) with an ACRP certification for CCRA and CP who developed the clinical program at Biotex and currently manages the Biotex CRO+. Since 2015, Britnee has managed several clinical investigations involving devices and drugs at various institutions and sites inside and outside the U.S., involving national and international travel. She is a reliable CRA with knowledge in all research areas, including clinical and regulatory requirements for a seamless U.S. or OUS EC/IRB approval. She is known for her strong ethics and commitment to quality patient care.
/ Clinical /

Tips for Writing a Protocol for Clinical Investigations

Tips for Writing a Protocol for Clinical Investigations

How do you write the perfect protocol for your clinical investigation? First, it’s important to understand what exactly a protocol is, along with its components.

ABOUT THE AUTHOR

Britnee Ochabski
Britnee Ochabski
Britnee Ochabski is a Senior Clinical Research Associate (CRA) with an ACRP certification for CCRA and CP who developed the clinical program at Biotex and currently manages the Biotex CRO+. Since 2015, Britnee has managed several clinical investigations involving devices and drugs at various institutions and sites inside and outside the U.S., involving national and international travel. She is a reliable CRA with knowledge in all research areas, including clinical and regulatory requirements for a seamless U.S. or OUS EC/IRB approval. She is known for her strong ethics and commitment to quality patient care.
/ Clinical /

The Importance of Grasping EC/IRB Fundamentals in Clinical Research

The Importance of Grasping EC/IRB Fundamentals in Clinical Research

Whether you’re a Sponsor, Data Coordinating Center (DCC), Contract Research Organization (CRO), investigational site, or other party involved in a clinical investigation, it’s essential to have basic knowledge of EC/IRBs.

ABOUT THE AUTHOR

Britnee Ochabski
Britnee Ochabski
Britnee Ochabski is a Senior Clinical Research Associate (CRA) with an ACRP certification for CCRA and CP who developed the clinical program at Biotex and currently manages the Biotex CRO+. Since 2015, Britnee has managed several clinical investigations involving devices and drugs at various institutions and sites inside and outside the U.S., involving national and international travel. She is a reliable CRA with knowledge in all research areas, including clinical and regulatory requirements for a seamless U.S. or OUS EC/IRB approval. She is known for her strong ethics and commitment to quality patient care.
/ Clinical /

How to Choose the Best Contract Research Organization (CRO) for Your Clinical Trial

How to Choose the Best Contract Research Organization (CRO) for Your Clinical Trial

Your product is in a crucial stage, requiring a thorough clinical investigation to further assess its safety and efficacy. It’s time to choose the best team to monitor your clinical investigation…

ABOUT THE AUTHOR

Britnee Ochabski
Britnee Ochabski
Britnee Ochabski is a Senior Clinical Research Associate (CRA) with an ACRP certification for CCRA and CP who developed the clinical program at Biotex and currently manages the Biotex CRO+. Since 2015, Britnee has managed several clinical investigations involving devices and drugs at various institutions and sites inside and outside the U.S., involving national and international travel. She is a reliable CRA with knowledge in all research areas, including clinical and regulatory requirements for a seamless U.S. or OUS EC/IRB approval. She is known for her strong ethics and commitment to quality patient care.