When you select the right CROs and effectively oversee their performance, you can be confident that your studies will meet regulatory standards and project timelines, paving the way for a smooth progression of your drug candidate to clinical trials and regulatory approval.
What can we do for you?
Within our longstanding global network, we are linked with a diverse array of key opinion leaders (KOLs), prestigious research institutes, and esteemed CROs with whom we have collaborated in the past and continue to collaborate at present. We operate independently; therefore, we can support an impartial and effective CRO selection process ensuring your non-clinical studies meet the highest scientific and regulatory standards.
Additionally, we provide support for ongoing study monitoring and CRO management which guarantees successful completion of contracted activities. Moreover, we review non-clinical study reports for inclusion into the regulatory submission(s).
Contact us to discuss how our tailored approach can support your regulatory requirements and advance your research objectives. Together, let’s shape the future of safer and more effective therapies.
Watch how we maintain the highest professional standards
Approach & Expertise
Learn how we can support you in meeting your business goals
- Our lean and powerful team with degrees in pharmacy, chemistry, biology, or related studies strive to be of added value to you. Our short reporting lines enable the most efficient road to your success.
- Having one point of contact from our experts backed by the team’s collective knowledge and resources we give reliable advice and execute projects seamlessly.
- At Starodub, consistency and assurance of quality are vital. A quality management system has been implemented and we adhere to GxP and ISO 9001/13485.
