... ...

Reduce costs for industry

Cost-effective solutions to streamline clinical research for the industry.

Access to scientific and Medical Experts

Direct access to experienced scientific and medical experts.

Rigorous Quality Assurance

Rigorous quality assurance to ensure compliance and data integrity.

...

Trusted By

0
k
About

The best choice for your research project

Hendosyn is a Clinical Research Accelerator (CRA) operating in LATAM since 2018, providing tailored research services outsourced on a contract basis. Our role is essential in the healthcare industry, supporting clinical development, clinical trial management, outcomes research, and commercialization.

Expert support

Contact support team

Quality Assurance

Best practice guarantee

...

Our company solutions

...
01
Leadership

Hendosyn provides medical and regulatory leadership in México with the highest quality in executing research studies.

Read More
...
02
Local Commercialization

Bridging the gap between development to commercialization of medications or medical devices in México

Read More
...
03
Clinical Trials

Collaboration between sponsors partners and local institutions to provide support services that deliver the availability of resources to execute research studies.

Read More
services ... ...

Our services are designed to streamline and enhance every phase of the clinical trial process. From early-stage protocol development and regulatory strategy to site activation, patient recruitment, and data management, we provide tailored support that helps sponsors and research teams reduce timelines, lower costs, and maintain high standards of quality and compliance.

Why choose us

Why us
  • Deep local expertise
  • Access to High-Performing Sites
  • Tailored Solutions

Deep Local Expertise with Global Standards

We combine in-depth knowledge of Latin American regulatory systems and healthcare networks with strict adherence to ICH-GCP and international best practices. This ensures your trial is efficiently executed and globally compliant minimizing delays and maximizing data integrity.

...
...

Access to High-Performing Sites & Diverse Patient Populations

We offer direct access to vetted, GCP-compliant research sites and treatment-naïve patients across Latin America. Our network enables faster recruitment, reduced costs, and more representative data—critical for both early-phase and large-scale trials.

Tailored, Cost-Effective Trial Solutions

Every sponsor is different—so we customize our services to your trial’s size, goals, and budget. From full trial management to targeted support, we provide scalable, flexible solutions that accelerate timelines without compromising quality..

...
...

Customer love us

feedback ... ...

Our team members

Expert Medical & Regulatory Leadership for High-Quality Clinical Research

We provide medical and regulatory leadership in Latin America with the highest quality in the execution of research studies.

...
...

Frequently asked questions

A Clinical Research Accelerator is a specialized service provider that helps sponsors and researchers speed up and optimize the clinical trial process—from study design and regulatory approvals to site management and data analysis.
We support biotech startups, pharmaceutical companies, CROs, and academic institutions conducting clinical trials in Latin America, particularly those looking for cost-effective, high-quality, and regionally adapted execution.
Our core focus is Latin America, where we offer deep regional expertise. However, we collaborate with global sponsors and can align our services with international standards for multicountry studies.
We support all phases of clinical research (Phase I–IV) across therapeutic areas, including vascular, oncology, cardiovascular, infectious diseases, rare diseases, and medical devices.
Our regulatory experts handle submissions to agencies like COFEPRIS, ANVISA, INVIMA, and DIGEMID, as well as ethics committees. We ensure all documents are accurate, complete, and submitted on time.
Yes. We offer site feasibility assessments, selection, contracting, training, and ongoing monitoring. All our partner sites are vetted for GCP compliance and performance history.
We use localized recruitment strategies such as physician referrals, digital campaigns, and community engagement, ensuring faster enrollment and better retention.
Absolutely. We can implement eConsent, ePRO, telehealth, and mobile health units to support decentralized or hybrid trial designs, even in hard-to-reach areas.
Unlike traditional CROs, we provide more flexible, faster, and cost-effective solutions with a strong focus on local partnerships, innovation, and sponsor collaboration.
You can reach out via our contact form or email. We’ll set up a discovery call to understand your needs and propose a customized plan to accelerate your clinical research goals.
... ...
;