Comac Medical
Comac Medical is a leading global Contract Research Organization (CRO) and Site Management Organization (SMO) dedicated to delivering high-quality clinical trial solutions across various therapeutic areas. With nearly three decades of experience, they focus on innovative, personalized, and efficient clinical research services from Phase I to Phase IV, including medical devices and food supplements. Their mission is to accelerate medical innovation and improve patients' quality of life through expert development services, smart solutions, and a commitment to quality, efficiency, and integrity. They support a broad spectrum of therapeutic areas including Psychiatry & Psychology, Pulmonology, Rheumatology, Urology, Allergy & Immunology, Cardiology, Dermatology, Endocrinology, Gastroenterology & Hepatology, Gynecology & Obstetrics, Hematology, Infectious Diseases, Nephrology, Neurology, Oncology, Ophthalmology, Orthopedics, Otolaryngology, Pain Management, Pediatrics, and others.
Industries
Nr. of Employees
large (251-1000)
Comac Medical
Products
Early Phase Clinical
Comac Medical's Early Phase Clinical Research Unit specializes in Phase I, Bioavailability and Bioequivalence (BA/BE) studies with over 18 years of expertise, located in Sofia, Bulgaria. It offers state-of-the-art facilities and a skilled team for efficient management of early phase clinical trials.
Early Phase Clinical Trials
Comac Medical offers early phase clinical trials combining over 18 years of expertise with state-of-the-art facilities to ensure precise and reliable results, specializing in Phase I and Bioavailability/Bioequivalence (BA/BE) studies.
Phase I Unit
A full-service integrated clinical trial unit specializing in early phase (Phase I) clinical trials, offering cost- and process-effective services with access to large drug-naïve patient pools and dedicated clinical and monitoring teams.
Comac Medical Early Phase Unit
A clinical research unit with over 15 years of experience and more than 200 completed clinical trials, strategically positioned in Sofia, Bulgaria, offering excellent research capabilities and top-tier amenities for volunteers.
Pan-European Contract Research Organization (CRO) Services
Comac Medical offers tailored clinical solutions for sponsors, providing comprehensive in-house clinical trial solutions from Phase I to Phase IV, including clinical investigation services for medical devices and food supplements.
Study Start-Up
Comac Medical offers tailored study start-up strategies including feasibility assessment, site management, regulatory affairs, documentation, training, and study submission management to ensure timely trial initiation within budget.
Early Phase Clinical
Comac Medical's Early Phase Clinical Research Unit specializes in Phase I, Bioavailability and Bioequivalence (BA/BE) studies with over 18 years of expertise, located in Sofia, Bulgaria. It offers state-of-the-art facilities and a skilled team for efficient management of early phase clinical trials.
Early Phase Clinical Trials
Comac Medical offers early phase clinical trials combining over 18 years of expertise with state-of-the-art facilities to ensure precise and reliable results, specializing in Phase I and Bioavailability/Bioequivalence (BA/BE) studies.
Phase I Unit
A full-service integrated clinical trial unit specializing in early phase (Phase I) clinical trials, offering cost- and process-effective services with access to large drug-naïve patient pools and dedicated clinical and monitoring teams.
Comac Medical Early Phase Unit
A clinical research unit with over 15 years of experience and more than 200 completed clinical trials, strategically positioned in Sofia, Bulgaria, offering excellent research capabilities and top-tier amenities for volunteers.
Pan-European Contract Research Organization (CRO) Services
Comac Medical offers tailored clinical solutions for sponsors, providing comprehensive in-house clinical trial solutions from Phase I to Phase IV, including clinical investigation services for medical devices and food supplements.
Study Start-Up
Comac Medical offers tailored study start-up strategies including feasibility assessment, site management, regulatory affairs, documentation, training, and study submission management to ensure timely trial initiation within budget.
Services
End-to-end clinical trial services including protocol development, regulatory support, clinical operations, site management, data management and biostatistics across early to late-phase studies.
Site-focused operational services including site activation, patient recruitment support, investigational product logistics and on-site coordination.
Dedicated Phase I inpatient unit services for first-in-human, bioavailability and bioequivalence studies with on-site pharmacy and supporting laboratory capabilities.
Scalable outsourced staffing and delivery of delegated functions such as clinical operations, data management and biostatistics to supplement sponsor teams.
End-to-end supply planning and logistics including forecasting, labeling, cold-chain management, depot distribution and direct-to-patient shipments with technology-enabled tracking.
Cross-functional protocol advisory including endpoint definition, feasibility assessment, QbD risk mitigation, stakeholder reviews and regulatory-aligned documentation support.
End-to-end clinical trial services including protocol development, regulatory support, clinical operations, site management, data management and biostatistics across early to late-phase studies.
Site-focused operational services including site activation, patient recruitment support, investigational product logistics and on-site coordination.
Dedicated Phase I inpatient unit services for first-in-human, bioavailability and bioequivalence studies with on-site pharmacy and supporting laboratory capabilities.
Scalable outsourced staffing and delivery of delegated functions such as clinical operations, data management and biostatistics to supplement sponsor teams.
End-to-end supply planning and logistics including forecasting, labeling, cold-chain management, depot distribution and direct-to-patient shipments with technology-enabled tracking.
Cross-functional protocol advisory including endpoint definition, feasibility assessment, QbD risk mitigation, stakeholder reviews and regulatory-aligned documentation support.
Expertise Areas
- Clinical trial design and protocol optimization
- Adaptive and complex trial designs
- Decentralized and hybrid clinical trials
- End-to-end clinical operations and program management
Key Technologies
- Clinical Trial Management Systems (CTMS)
- Interactive Response Technology (IRT) and randomization systems
- Electronic data capture and decentralized trial platforms
- Real-time shipment and temperature monitoring
News & Updates
Participation in the EBF Autumn Conference 2025 on 18–19 September 2025 in Malaga, Spain.
Participation in the inaugural OCT China 2025 event on 3–4 September 2025 in Suzhou, China.
Participation in the PCMG Annual Assembly from June 10–12, 2025, in Malaga, Spain.
Participation in the BIO International Convention from June 16–19, 2025, in Boston, USA.
Participation in the American Society of Clinical Oncology (ASCO) Annual Meeting from May 30 – June 3, 2025, in Chicago, Illinois, USA.
Participation in the UK & Ireland 2025 event on June 10–11, 2025, in London, UK.
Participation in the EBF Autumn Conference 2025 on 18–19 September 2025 in Malaga, Spain.
Participation in the inaugural OCT China 2025 event on 3–4 September 2025 in Suzhou, China.
Participation in the PCMG Annual Assembly from June 10–12, 2025, in Malaga, Spain.
Participation in the BIO International Convention from June 16–19, 2025, in Boston, USA.
Participation in the American Society of Clinical Oncology (ASCO) Annual Meeting from May 30 – June 3, 2025, in Chicago, Illinois, USA.
Participation in the UK & Ireland 2025 event on June 10–11, 2025, in London, UK.