Matching our clients' needs

Richmond Pharmacology’s data management solution recognises the diversity of our clients’ preferred methods of collecting, analysing and reporting clinical data. By listening and understanding these preferences we can adapt our standard processes to meet the needs of our clients.

x

Richmond Pharmacology can manage your data management activities as standalone contract.

Our promise is accessibility, we guarantee your data is available and accessible when you need it.

Security and data protection: Your data is protected with advanced eCRF platform and encryption and comprehensive managed services.

Richmond Pharmacology can be your partner in undertaking all clinical data management activities from protocol review to database lock and delivery of statistical outputs.

Our credentials

Our data management solution boasts a highly proficient Clinical Data Management team with a vast experience in the clinical research sector, covering the pharmaceutical, biotechnology and CRO industries.

Our team, our commitment

Our team have academic backgrounds with industry experience in all phases of clinical trials across numerous therapeutic areas. Our expert statisticians are involved in all aspects of a project from protocol and eCRF design to statistical reporting.

Get in touch today

Why choose Richmond Pharmacology for your data management needs

TAP OR CLICK A BLOCK BELOW TO LEARN MORE

Accredited provider

We work to the highest clinical standards to guarantee the delivery of quality data in line with set turnaround times and within budget.

Read more +

Live data at each stage of your trial

We create a consistent experience in one location.

Read more +

Eliminating inefficiencies

The data management team are on hand to consult throughout the study cycle, managing every aspect from the data handling plan to data extraction.

Read more +

Accurate timeline & cost predictability

Our extensive metrics and feasibility assessments offer invaluable insight into study acceptability and suitability.

Volunteer experience

By listening to the feedback of our volunteers, we make continuous improvements to the experience of our research participants.

Learn from every engagement. Aggregated data solutions which enhance the clinical research process.

Latest news

Director of Operations, Keith Berelowitz, has been appointed as the Research Ethics Committee Chair for the Health Research Authority.

January 19, 2023
Keith Berelowitz will be responsible for ensuring that all ethical possibilities are explored in relation to new research.
Read more

Unlocking the potential of data sharing

January 4, 2023
Dilshat Djumonov explores how GDPR is central to protecting private information while presenting unique challenges to the pharmaceutical clinical trials industry.
Read more

Events

13th International Workshop on Regulatory Requirements and Current Scientific Aspects on the Preclinical and Clinical Investigation of Drug-Drug Interactions

Sunday, June 4th to Tuesday June 6th 2023
Exchange research-based knowledge on drug-drug interactions (DDIs) among all interested stakeholders from pharmaceutical industry, regulatory authorities, academic and health care delivery backgrounds and perspectives.
View event