thinqbetter specializes in medical device and IVD product registrations in Europe and the USA. For this purpose, they offer consulting and services throughout the entire product life cycle. Through their internal expertise and cooperation partners, the most complex projects can be realized.
Their satisfied clientele includes companies with double-digit billion euro turnovers, as well as start-ups with 1-2 employees.
Starodub BV offers comprehensive support for (bio)pharmaceuticals and medical devices throughout their lifecycle. For (bio)pharmaceuticals, we efficiently guide the development and registration of medicinal products, including small molecules, biologics, biotechnology-derived products, ATMP and vaccines. With a strategic approach focusing on a helicopter view, we address potential opportunities, risks, and solutions. Our services cover various applications, regulatory frameworks, and interactions with global health authorities, promoting quick market access and cost-effectiveness.
In the medical device sector, Starodub BV facilitates the development and registration of class I to class III devices, including software, in vitro diagnostic products, and drug-device combination products. We assist in establishing ISO 13485 compliant quality management systems, ensuring efficiency in time and cost. The company’s four-pillar approach emphasizes maintaining a strategic overview, identifying opportunities, communicating risks, and finding optimal solutions. Services include qualification, classification, design, development, marketing, clinical/performance evaluation, risk management, post-marketing activities, and regulatory intelligence. Starodub BV also provides tailored training programs and regulatory operations support.
Holochem is a customer-oriented CRO offering chemistry manufacturing and control services for the development of fine chemicals and drug substances for the pharmaceutical chemistry, animal health, cosmetics and agro-sciences industries. Holochem provides R&D services for the development of small and complex molecules, key intermediates, and APIs, highly potent APIs & ADC linkers, impurities, metabolites and reference standards. We produce non-GMP pre-clinical batches from milligram to kilo-scale for early-phase formulation and toxicological use.
Invisio is your partner for national and international clinical phase 1 to phase 4 studies at medical practices and clinics without their own research department.
As an interface between sponsors and CROs, as well as physicians and patients, we have been enabling national and international clinical studies for about ten years. For this purpose, we work together with more than 120 trained Flying Study Nurses and CRAs. They support physicians 365 days a year at all times to implement on-site clinical study projects in compliance with international quality standards.
We specialize in providing project management for clinical multicenter studies and, at the same time, implementing study projects at several trial centers throughout Europe. We are available without restrictions to our customers and all other persons involved in a study as a contact partner.
JBD HealthCare is a Medical Technology strategy consultancy firm that focuses on development, product management, implementation and go-to-market of different Digital Health solutions. Our core of expertise is in the usage of data and Digital Biomarkers applied to clinical medicine or Research.
PHARMAPOINT S. A. is a part of Pelion Healthcare Group as a part of the wholesale business line provides clinical trials logistics services including: market research; documentation gathering and analysis; product sourcing and acquisition; product storage including ambient and cold chain stock in accordance with GDP; logistic and distribution support; product kitting, labelling and repacking.
The range of services is constantly enlargened and adjusted to changing market conditions. We are open to new forms of cooperation and continually analyze trends on the pharmaceutical market to meet the expectations of our business partners.
ARENSIA has its own network of nine state of the art exploratory medicine units with full Phase I / II / PROOF OF CONCEPT patient capabilities. These modern units are located within dedicated areas in prestigious University Hospitals in Romania, Republic of Moldova, Georgia, and Ukraine.
ARENSIA has been building deep relationships with each of the hospitals where our units reside. This has allowed ARENSIA to achieve industry leading recruitment rates across a number of therapeutic areas, whilst still maintaining the highest resulting data quality.
Quinta-Analytica is well recognized one-stop-shop company offering full package of the services in Phase 1 Clinical testing, Bioanalytical testing, Pharmaceutical analyses including analytical development and stability testing.
Quinta-Analytica was inspected by FDA more than 10 times already with no findings. Besides of above mentioned, we offer also expertise in batch release, analytics of inhalers, peptides and proteins (large molecule analyses generally including biosimilars) as well as consultancy in Regulatory and Clinical Strategy. We are located in Prague, Czech Republic.
Quinta-Analytica operates in full compliance with GCP/GLP/GMP and also FDA standards. Due to joint-venture laboratory located in Russia we can support our business partners also in terms of their needs of pre-clinical and clinical studies on Russian market.
Rephine is a firm of deeply experienced GxP consultants, auditors and practitioners. The company proactively helps pharmaceutical, biotech and medical device companies with all aspects of their manufacturing and supply chain quality assurance and associated business process optimisation.
Widely acknowledged to be the gold standard in its field, Rephine has been providing these specialist quality assurance services for more than 25 years. Rephine is a founding member of 3PARL®, a consortium that aims to set a new benchmark for consistent, reliable, high-quality supply chain Good Manufacturing Practice (GMP) audit services and library reports.
At Pharma Professionals we have developed capabilities to support clinical trials with home-care services that help enhance the quality of patients’ lives while maximizing recruitment and retention for our clients.
Our GCP-trained personnel visit patients at their homes or work and are responsible for activities including sample collection, vital signs documentation, study-drug administration, monitoring changes in patient health, and visit documentation.
We also deliver a wide range of staffing solutions to Pharmaceutical, Biotechnology, and Clinical Research Organisations as well as Medical Device and Diagnostics companies across Europe.
We recruit professionals who work with human as well as animal-health products, including pharmaceuticals, vaccines and biologics in addition to consumer health products.
We serve both innovative and generic clients. We work with both corporate organizations listed among top 50 global pharmaceutical and biotechnology companies as well as with midsized and small life-science companies.
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