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Research Drive will help you to select the most suitable pharmacology unit or clinic to conduct your trial from first-in-human.

To ensure fast study start-up, we take care of your regulatory submission until clinical trial approval. We have close collaborations with Ethics Committees of clinical pharmacology units or hospitals.

We perform independent monitoring and go for the extra mile for your clinical trial to safeguard highest quality, integrity of data, compliance and subjects/patient safety.

Our team provides dedicated and flexible services depending on the clients’ needs, with a personalised and tailored approach.

Research Drive has audited SOPs in place, including a specialised Phase I SOP.

Research Drive’s specialised staff can be contracted for short and long-term assignments. Our team includes Clinical Trial Assistants (CTA), Project Managers (PM), Clinical Research Associates (CRA) and Regulatory Specialists.