Successful execution of clinical trial programs that address the specific trials required for approval. We advise on the appropriateness of each study and manage critical path issues, which may impact on the clinical development program.

Abingdon recognizes that pro-active project management is the key to success of all clinical studies, and manages this critical activity with processes designed to incorporate quality into the entire program. In addition to our experienced and highly trained PMs, Abingdon’s processes require that the Executive Team support and share the responsibility for ensuring a successful on time and within budget completion of your study. The Project Manager is responsible for ensuring you are kept fully conversant with all aspects of your study via Progress and Tracking Reports, conference calls and many other forms of communication.

As an integral member of the Project Team, Abingdon’s Clinical Monitors are clinically knowledgeable and trained to ensure consistent and quality monitoring.

Beginning with input to clinical protocols and clear, concise statistical analysis plans, Abingdon’s statisticians provide our clients with quality and timely deliverables. Our statisticians work closely with the medical and regulatory teams to ensure that all the strategies are integrated towards a successful outcome of a single study or an entire development plan.

Abingdon’s medical writing team produces clear, concise documents that meet the regulatory requirements. From the preparation of INDs via protocols, Investigator Brochures and clinical study reports to NDAs/MAAs our services are available as part of a full drug development program or as individual items.

Our experienced Pharmacokineticist can provide clients with clinical PK development programs, bioanalytical data review and interpretation, PK modeling and PK reports