Keeping your preclinical studies on track and on time

Preclinical studies are essential in the drug development process to ensure that the drug candidates are safe and effective before entering clinical trials. To be successful, preclinical studies require efficient management and effective communication among all stakeholders involved in the process. Therefore, a capable test site, a detailed study plan, ethical and regulatory compliance, and proper documentation, are essential for smooth execution.

PROMAFUN CRIO has the skills necessary to manage your project, such as Planning and organization, Communication, Risk management, Budgeting, and financial management.

Why Study Management Matters

Preclinical studies involve multiple stakeholders, strict timelines, and regulatory requirements. Without effective management, studies risk delays, budget overruns, or miscommunication.

Our Service

What we deliver:

• End-to-end planning and oversight
• Communication with CROs and stakeholders
• Risk identification and mitigation strategies
• Budget and timeline control

Our support ensures that your study remain on track, scientifically rigorous, well-coordinated, and delivered on time.

How We Work 

We act as the central coordinator between your team and CRO partners, ensuring studies progress smoothly and challenges are addressed proactively.

Contact Form

Let’s streamline your study.
Tell us about your protocol, timelines, and sites. Our team will get back to you within 48 hours.