Epiontis GmbH (now Precision for Medicine)

MONIPOL offers a full range of clinical development and consulting services to a strong customer base of mainly small and medium-sized pharmaceutical, biotechnology, and medical device companies. We are best at tailoring services to your needs.
- Offices in Poland, Germany, and Switzerland.
- ISO 9001:2008 certified.
- GCP-Audits, System-Audits.
- Data Management - Our comprehensive Clinical Data Management solution provides a seamless data collection process, from rapid database launch to high-quality data deliverance, using industry-leading EDC technologies.
- Feasibility - Our local teams offer a deep understanding of the regional clinical dynamics, working alongside you to devise an optimal strategy for your study and identifying ideal trial sites through detailed feasibility studies.
- Functional Service Provisioning - Project Management, Monitoring, Regulatory
- Medical Writing - Our medical writers, drawing on broad industry and academic knowledge, produce timely, cost-effective clinical and regulatory documents, transforming complex data into an accurate, evidence-based account of your drug’s clinical profile.
- Study Start-up - Our study team collaborates with selected sites to collect essential documents, finalize clinical study agreements, and manage submissions and document preparation in parallel, ensuring maximum site initiation at the study’s outset.

OPIS is a European clinical CRO providing premium support for the management of global clinical trials from phase I to IV as well as pre- and post-marketing medical device investigations.
Founded in 1998, the company has 20 years of extensive experience in a wide range of therapeutic areas. Its recent oncology/immuno-oncology portfolio amounts to over 400 trials.
OPIS’s strength lies in its people and its specialized teams who assist clients from A-Z with medical writing, scientific and statistical consultancy for trial design and skilled teams of operational staff across Europe that ensure high quality project execution.
The OPIS e-clinical suite is developed to streamline digitalization of clinical data. Fully FDA 21 CRF Part 11 compliant and developed in close collaboration with the OPIS biometry and clinical operations units it offers:

• CLINICAL.NET, a modular and extremely user-friendly platform to handle all clinical trial data.
• A consolidated platform to handle named-patient programmes digitally.
• An investigator toolkit to facilitate and coordinate patient and clinician participation in clinical trials.

With flexible business models, OPIS clients come first and offers are truly shaped around individual Sponsor needs.

The OPIS teams are passionate about what they do and OPIS wants its name to stand for excellence.

PPD is a leading global contract research organization providing comprehensive, integrated drug development, laboratory and lifecycle management services. Our customers and partners include pharmaceutical, biotechnology, medical device, academic and government organizations. With more than 28,000 professionals worldwide, PPD has conducted clinical trials in more than 100 countries to help customers deliver life-changing therapies to improve health. We apply innovative technologies, therapeutic expertise and a firm commitment to quality to bend the cost and time curve of drug development and optimize value. For more information, visit www.ppd.com.

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Employment and Careers
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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

We deliver vital health information, at the time it matters.

High-tech company for innovative laboratory diagnostics and research services with strong focus on Rare Diseases and Newborn Screening. From Inborn Errors of Metabolism to Oncology we make personalized diagnostics more accessible.
We provide everything from routine tests to clinical studies and from biochemical to genetic testing.
We are dedicated to the development of novel laboratory tests that make actionable health information fast accessible.

Clinical Mass Spectrometry, Next-Generation Sequencing and development of novel assays and biomarkers for routine services and clinical research.
International Diagnostic Services for Biotech & Pharma companies.
ARCHIMEDlife Research Institute for academic research, - omics and biomarker discovery.