Biocair

Biocard is a full service contract research organization (CRO) and a full cycle logistics company. We can accommodate a full spectrum of your potential requirements when dealing with clinical trials in CEE region: feasibility, regulatory, monitoring, project management, customs clearance, logistics and courier services.

• Over the years we trained ourselves to strictly follow the essential guiding principles of our industry: GCP, GMP, GDP, GSP and our SOP’s.

• Biocard provides full cycle logistics services in Russia and some of the former CIS countries.

• Worked with 14 out of top 20 pharmaceutical companies in the world.

• Conducted more than 350 clinical studies and went through 320 audits.

• We hold ISO 9001 certificate and local Russian pharmacy license.

• Our total industry experience exceeds 23 years.

• And we can do customs clearance under 24 hours!

CRMG is a clinical development services organization, focused on providing biotech and pharmaceutical companies with an assortment of services tailored to support clinical development programs from Phases I – IV.

Our organization’s foundation was built on our formative experiences in biotech, which allows our clinical and medical professionals to understand what it’s like to sit on our client’s side of the table, and to use that experience and knowledge to help plan and execute your study in a highly collaborative environment.

Flexibility in our service offering allows our clients to take advantage of CRMG’s capabilities to balance their business needs no matter what phase of development they are at. Whether it be consulting, clinical operations, medical/safety, regulatory or clinical supply logistics services, CRMG provides the right level of expertise and resources to successfully deliver your study on time and within budget.

Cromos Pharma is an international CRO with expertise in delivering all aspects of clinical trials in all clinical phases and a range of therapeutic areas.

Cromos Pharma offers fully integrated CRO services including regulatory consulting and compliance, project management; monitoring; medical writing; data management and biostatistics; drug and device registration services; logistics and warehousing; post-marketing services and independent audits. Cromos Pharma delivers rapid recruitment and excellent patient retention as well as expert study design and management.

Cromos Pharma's "No Patients - No Payments"​ initiative allows the sponsors to pay for performance and is our guarantee that the study timelines will be met.

Established in Moscow in 2004, Cromos Pharma has strong regional presences in Central and Eastern Europe, Russia and Post-Soviet Bloc countries. Its European HQ is situated in Dublin, Ireland and its US base is in Portland, Oregon.

Mediolanum Cardio Research (MCR) Srl is an independent Contract Research Organisation (CRO) established in Milano (Italy).
MCR was founded in 2002 with the aim of supporting no-profit research projects developed by a group of interventional cardiologists. Since then MCR have gained extensive experience as Clinical Research Organization providing services for regulatory authorizations, project management, monitoring, data management and statistics for sponsored and no-profit clinical trials both pharmacological as well as with Medical Devices.
MCR is well structured and fully staffed to manage projects in full compliance with GCP and applicable regulations. MCR can supports Sponsors and researches in all stages: protocol preparation, logistic organization, regulatory processes, clinical monitoring, pharmacovigilance, data cleaning and analysis, and data reporting. MCR has also internally developed an electronic CRF, compliant with FDA 21 CFR part 11 (called IDAS).
In addition, MCR has an internal Core-lab specialised in QCA readings.

OCT is the leading contract research organization in Russia. Since 2005, OCT’s team has conducted over 300 clinical trials in Eastern Europe and the CIS region. Our team of 150+ clinical professionals provides a full range of high-quality CRO services for Phase I-IV and BE studies, with therapeutic expertise in oncology, infectious disease, and all major therapeutic indications.

As pharmaceutical and biotechnology companies have turned toward outsourcing models in clinical research, OCT has established itself as one of the top contract research organizations worldwide. With strong local expertise and focus on quality, OCT ensures seamless clinical trial conduct and drug registration, on time and within budget.

Our experienced team delivers a full range of CRO services:

Clinical Study Design Preparation
Medical Writing
Consulting and Regulatory Support
Project Management and Monitoring
Drug Safety and Pharmacovigilance
Data Management
Biostatistics
Clinical Supply Services and Logistics
Marketing Authorization
GMP Inspection Support