We'd love to hear from you. Tell us about your project and we'll get back to you promptly.
Whether you need an audit, want to enroll in a training course, are looking for a CRO partner, or want to discuss patient recruitment — we're here to help.
We audit Phase I–IV clinical studies, observational studies, and post-marketing surveillance studies. Our audits comply with ICH GCP E6(R2) and applicable regulatory frameworks.
Yes. All our courses are certified by the Ministry of Education of the Republic of Moldova, granting them official status for professional development and regulatory compliance purposes.
Authorization timelines depend on the study type and regulatory pathway. We guide sponsors through the full process and provide realistic timeline estimates during initial consultations.
Absolutely. Our CRO and patient recruitment services are specifically designed for international pharmaceutical companies and sponsors seeking to conduct studies in Moldova.