Boyds strengthens team with regulatory operations and publishing expertise
Boyds is pleased to announce the appointment of regulatory operations and publishing professional Michelle Hackney to lead our new in-house Regulatory Operations offering.
Michelle has over a decade of specialist experience in publishing and regulatory operations, having previously held team leader roles at regulatory consultancy DLRC Ltd and Teva Pharmaceutical Industries.
As Associate Director, Regulatory Operations at Boyds, Michelle will lead and manage all aspects of Regulatory Operations, responsible for the planning, coordination, and execution of tasks relating to the development, submission, and maintenance of regulatory documents necessary for the approval and post-approval lifecycle of drugs, medical devices, and other healthcare products. She will also lead the implementation of our industry-leading publishing software – LORENZ docuBridge.
Commenting on her appointment, Michelle said: “I am thrilled to be supporting Boyds with its new in-house Regulatory Operations offering and helping to enable the team to support the full lifecycle of projects for its valued, global client base. Boyds has an excellent reputation in the industry for its regulatory expertise, and I am looking forward to bringing my eCTD global publishing knowledge and regulatory submissions knowledge to further support clients on their drug development journeys.”
To find out more about the Regulatory Operations service, click here.
