OUR CRO SERVICES

ESTERN Medical CRO Life Sciences offers an extensive suite of clinical trial research and development services within the pharmaceutical and medical device sectors, spanning two continents— the United States (North America) and Latin America (South America).

We take pride in our proven track record of effectively managing programs across all phases of clinical development. In Phases I and II, our studies involve both healthy volunteers and patient populations with specific medical treatment conditions.

What distinguishes ESTERN Medical is our strategically positioned Phase I units within hospitals, facilitated by international partnerships. This strategic placement enables us to rapidly recruit patients and volunteers.

In Phases II and III, ESTERN Medical has successfully executed pivotal trials, resulting in regulatory approvals from FDA, EMEA, LATAM, and/or international regulatory bodies.

During the late Phase IV stage, we collaborate with sponsors in the post-approval process, meticulously planning and executing large, straightforward studies, registries, outcome studies, and risk management programs.

Our Clinical Research Services

Clinical Research Development & Regulatory Services

Surpassing other Clinical Contract Research Organizations and Development Resources, ESTERN Medical CRO Life Sciences confronts and resolves Clinical Research and Development (R&D) and Regulatory risks with an extensive portfolio of knowledge-based solutions.

Our highly responsive team of professionals customizes a tailored package of services based on your specific sponsor needs, leveraging our broad expertise and knowledge in both the US (North America) and Latin America. ESTERN Medical also extends its comprehensive CRO services to local Latin American emerging markets, including Mexico, Colombia, Brazil, Peru, Chile, and Argentina.

From early R&D clinical development and regulatory stages through late-phase clinical trials, ESTERN Medical provides an all-encompassing range of integrated product development services. Regardless of your point of entry into our resources, we craft a personalized clinical and regulatory program, granting seamless access to our full spectrum of development services tailored to meet your specific requirements in the US (North America) or Latin America.

Choosing ESTERN Medical allows you to mitigate risks, optimize clinical and regulatory development processes, and provide your team with a competitive edge in accessing novel insights and solutions. Off-load tasks while uploading valuable knowledge assets and expertise with ESTERN Medical.

Cookies acceptance

At ESTERN Medical, we use cookies to enhance your experience on our website and to ensure its proper functionality. By continuing to browse our site, you agree to our use of cookies.

For more information about how we use cookies and your rights, please see our Legal Policies.