Advancing Health Through Clinical Research

Innomed Research Ltd is a Site Management Organization (SMO) dedicated to supporting clinical trials with excellence, transparency, and compassion. We partner with hospitals, investigators, and sponsors to ensure high-quality, patient-centered research across Bulgaria.

About Us

Innomed Research Ltd. was founded in 2025 in Shumen, Bulgaria. Our organization operates across the city and collaborates with several medical centers, providing comprehensive support for clinical trials. Through our network of experienced investigators and medical specialists, we ensure access to diverse patient populations, helping sponsors and CROs conduct studies efficiently and reliably.

We combine professionalism with a friendly, collaborative approach, making it easy for partners, investigators, and patients to work with us.

Our Mission

Lead and support clinical trials with excellence, strictly adhering to ICH-GCP guidelines.
Uphold highest ethical and professional standards in all study activities.
Ensure efficient, reliable, and safe study execution through well-documented operational processes and SOPs.
Safeguard patient safety and study integrity while helping our partners achieve their objectives.

Specialties & Sites

Innomed Research has developed a flexible network of investigators and sites covering a broad spectrum of therapeutic areas, with the ability to expand according to the needs of each project. Our specialties currently include:

Ophthalmology

Gynecology

Pediatrics

Pulmonology

Urology

Internal Medicine

Oncology

Surgery

Ent (Ear, Nose, Throat)

Orthopedics

Dermatology

Dental Medicine

General Practice

with the flexibility to expand according to project needs.

We operate several centers in Shumen, providing convenient access to patients and facilitating smooth study conduct across multiple locations.

Our Team

Our team is composed of highly motivated and experienced professionals who bring together clinical expertise, research knowledge, and operational excellence. Key features of our team include:

Investigators: Many of our principal investigators have extensive experience in clinical trials, while others bring decades of practice treating large patient populations. This combination ensures both deep medical knowledge and a practical understanding of patient recruitment and retention challenges.
Coordinators & Study Staff: Skilled in managing the day-to-day operations of clinical trials, including patient scheduling, study monitoring, source documentation, and adherence to protocol.
Technical Specialists: Responsible for the maintenance, calibration, and troubleshooting of all clinical equipment and laboratory instruments, ensuring reliable and accurate data collection.
Contracts & Regulatory Team: Handles all agreements, ethics submissions, feasibility assessments, and communications with sponsors and CROs, ensuring studies run smoothly from start to finish.
Quality & Training Team: Designs and implements training programs for investigators and site staff, ensuring that all personnel are competent, confident, and up to date with GCP, SOPs, and study-specific procedures.

Our Goals

Deliver professional and reliable trial management in full accordance with GCP guidelines.
Build long-term partnerships with CROs, sponsors, and investigators based on trust, transparency, and shared success.
Support investigators and site staff through tailored training, guidance, and operational coordination.
Expand our therapeutic expertise and investigator network to accommodate diverse and evolving research needs.
Prioritize patient safety, ethical standards, and high-quality study outcomes in every project we undertake.