Adjutor Clinical
Clinical trials are a critical phase in drug and device development, transforming innovative concepts into safe and effective treatments.
At Adjutor Clinical we partner with businesses to design, manage, and deliver clinical development programs. We focus on generating the high-quality evidence needed to support regulatory approvals and maximises market access and licensing potential.
CLINICAL TRIAL
PREPARATION:
We handle all aspects of clinical trial preparation, from planning and protocol development to securing permits and ensuring regulatory readiness, so your studies start on the right track.
Adjutor Clinical provides the following services during the initial clinical stage:
Target Product Profile (TPP) & Clinical Development Plan (CDP)
Clinical strategy, key opinion leader and investigator identification
Protocol development
Investigator Brochure (IB) preparation
Informed Consent Form (ICF) preparation
Clinical readiness assessment
Study and country feasibility assessments
Site feasibility and selection
Ethics, governance and clinical regulatory submissions
Trial Master File (TMF) set-up
Statistical Analysis Plans (SAP)
Data management
Management of investigational products
Import permits, OGTR, ODC and other permits
The secret of success is to do the common thing uncommonly well.
John D. Rockefeller
Ready for growth?
Contact us today and let’s work together to achieve your goals. Whether you have a question, need more information, or want to discuss your project, our team is here to help.