Ad Hoc Clinical

Accell Clinical Research is an international full-service Contract Research Organization (CRO) managing Phase I-III clinical trials for 10+ years across Eastern Europe. With local presence, including highly qualified medical staff and legal entities in the region, we successfully recruit patients both in EU and outside EU in post-Soviet countries (CIS). All together we provide guaranteed fast patient recruitment in 20+ countries across the region.

⬇︎ ACCELL'S SERVICES for Phase I-III clinical trials:

• Strategic guidance and trial set-up:
• Feasibility research and site selection
• Study documentation development
• Regulatory support
• Clinical supply import and management
• Selection and management of clinical study vendors
• Project management
• Clinical & medical monitoring
• Data management and biostatistics
• Quality assurance
• Safety management
• TMF/eTMF services
• Functional outsourcing of a clinical team

⬇︎ THERAPEUTIC AREAS
• Oncology
• Cardiovascular
• Immunology
• Gastroenterology
• Neurology
• Endocrinology

ANTAEA Group of Companies is one of the largest Regional Clinical Research Organizations (CROs), providing high quality support in Southeast Europe, North Africa, Middle East and the Gulf Area.

The Group provides professional, yet flexible solutions, supporting our Clients to maximize their Research resources, in a cost effective manner. ANTAEA is dedicated to Services of scientific quality, management expertise, precision and reliable technology.

The Group includes integrated, marketing consultation services in our portfolio, based on Market Research, which cover products throughout their life cycle.

Specialities: Feasibility Projects, Initial Submissions, Amendments and Notifications to ECs (local and central) and Regulatory Authorities, Clinical Trials Monitoring in several different phases, Contracts for Clinical Trials Management, Contracts for Clinical Trial Rescue Projects, Design and Development of Clinical Trials Projects, Investigator Initiated Projects, Regulatory & Registration Projects (National, MRP, Variations etc.), Statistical Projects, Contracts for Investigator Training, Contract for Regulatory Services Training, Contract for Site Audit

ANTAEA also provides experienced CRAs to the Pharmaceutical and Biotechnology Industries and to CROs, in all the countries where ANTAEA is operating. ANTAEA training on procedures and setting standards and our technical support, guarantee uniformity in quality and timely delivery of projects.

SynCon International is a clinical research consultancy, specialised in the emerging regions.

SynCon International offers clinical research services, as well advice and expert support in the areas presented below:

- Clinical trials services in the emerging markets of CEE, Russia, Byelorussia, Kazahstan and Latin America

• Feasibility analysis
• Site identification
• Identification of investigators
• Investigator Contracts
• Regulatory Authority Submission
• Logistics (translation, meeting organization, etc.)
• Patient recruitment and retention strategies
• Monitoring
• Stats and Data Management
• Clinical Trial Compliance Management

- Recruitment and outsourcing of clinical trial personnel CEE, Russia, Byelorussia, Kazakhstan and Latin
America

- Strategic business development consultancy

Founded in 1997, Ergomed plc is a global provider of high-quality services to the biopharmaceutical industry, spanning all phases of clinical trials, post-approval pharmacovigilance, and medical information. Ergomed’s fast-growing services business includes an industry-leading suite of specialist pharmacovigilance (PV) solutions, integrated under the PrimeVigilance brand, and Ergomed Clinical Research, a complete, global Phase I-IV clinical development and trial management services with a strong heritage in the development of drugs in rare diseases and oncology.

• 1 300+ highly qualified professionals
• Global full-service CRO
• 24+ years of experience
• Therapeutic specialization in oncology
• Strong expertise in rare disease trials
• Robust clinical safety system
• Choice of leading drug safety databases

Our key services include:
• Clinical Research Services
• Pharmacovigilance
• Medical Information
• Regulatory
• Medical Writing
• Site Management
• Study Physician Support
• Biostatistics
• Patient Study Support

IRW is a Nordic full-service Clinical Research Organization (CRO) with more than 20 years experience and we are established in local offices in Stockholm, Gothenburg, Oslo, Copenhagen and Helsinki.

The IRW team is dedicated and professional, with a wide range of academic competence and solid experience of clinical research, Pharmacovigilance, Data Management and Biostatistics, as well as of working with global pharmaceutical and biotech companies, and of interacting with the various regulatory authorities in the Nordic region.

We can manage your project from start to finish, or function as a fully-integrated part of your team.

In all Nordic countries, experienced native-speaking experts handle all regulatory and ethical submissions, as well as local literature search, monitoring services and support to site etc. This, together with an excellent network, will speed up the regulatory processes, as well as facilitating communications with authorities, sites and investigators/physicians.

Being a local Nordic CRO, we can provide you with our wide-ranging knowledge on local requirements and local networks.

Please feel free to contact us for a dialogue regarding your clinical trial needs at +46 8 791 66 40.