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» Clinical Trial Software by Simplified Clinical
Simplified Clinical provides world class clinical trial software as a service (SaaS). We partner with sponsors, CROs, consortiums, and consultants to implement a standard platform to maximize trial results. Our clients include medical device companies, life sciences and biopharmaceutical leaders, universities and teaching hospitals.
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Our clinical trial solutions empower biopharma, medical device and CRO organizations to accelerate development. Contact us for trial management services.
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Global CRO enhancing clinical trial outcomes and optimizing vendor oversight with data-driven services and solutions including biostatistics and programming, clinical data management, medical writing and a portfolio of eClinical technologies.
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Zeta CRO is specialized in clinical trials for medical devices; biostatistics; data collection, management and analysis; clinical and statistical reporting. It is the only CRO accredited by AIFA in Friuli Venezia Giulia.
BECRO CRO Greece - Contract Services Organization - Clinical Trials - Bioequivalence Studies - Therapeutic Equivalence - Medical Devices
BECRO CRO Greece - Contract Services Organization - Clinical Trials - Bioequivalence Studies - Therapeutic Equivalence - Medical Devices
Your clinical trial at the next level
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Clinical Research (PTY) Ltd.
LT Clinical Research, is an independent contract healthcare research organization providing clinical trials management services in Africa, including GxP consulting for pharmaceutical, biotechnology, and medical devices companies.
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Onorach - a leading Contract Research Organisation (CRO) offering our clients a full range of services to efficiently and cost-effectively
Onorach are a leading Contract Research Organisation (CRO) and focus on the unique challenges of **** discovery, biopharmaceutical and medical device development, offering our clients a full range of services to efficiently and cost-effectively manage the clinical trial development process.
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Anagram is a Clinical Research Organization (CRO) based in Spain which provides high quality international services in clinical development and post-authorization trials with drugs and medical devices. Anagram is the first Spanish Imaging CRO which incorporates Imaging Core Lab services.
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MMS holdings is a leading global data-focused CRO (Clinical research organization) & technology enabled clinical research and health data analytics solution company that supports the pharmaceutical, biotech, and medical device industries.
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McDougall Scientific - 40 years as a niche Clinical Research Organization (CRO); specialized in BioStatistics, Clinical Trial Design, Data management.
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Think-i offers analytics, Forecasting, pharmacovigilance, clinical trials, regulatory & medical writing solutions to the pharmaceutical companies and medical devices companies.
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Clinical trials can be complex. ClinTrialConnect helps educate patients about clinical trials and their disease. In addition, it provides background information about the pharmaceutical or medical device company, and detailed information about what to expect from a specific clinical trial.
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Emergo: medical device consultants for QA/RA, device registration, clinical trials, reimbursement and distribution consulting. Offices worldwide.
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Within this company, training, consultancy and support is offered for manufacturers and healthcare professionals that are involved in clinical trials with medical devices.
Rianne Tooten | Clinical Research Professional | Training & Advice
Within this company, training, consultancy and support is offered for manufacturers and healthcare professionals that are involved in clinical trials with medical devices.
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Top Clinical Research Organizations | Full-Service CRO Company | Clinical Data Services | Quality Data Services, Inc
Quality Data Services, Inc is one of the best full-service CRO companies in the industry. If you’re looking for a company that offers medical device research & CRO pharmacovigilance services, contact us today!
CRO Contract Research Organisation Australia | Sydney | Melbourne | Brisbane | ISO 9001 Certified
Australia's favorite CRO providing quality full service clinical trial support to local and global medical device, pharma and biotech companies since 2008.
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PHC - Pharma & Health Consulting focusing on services within Pharma/ Medical device/Biotech and the Health-area. PHC Pharma & Health Consulting A CRO with a solid business concept and operations based on concrete business ethics criteria. Clinical Trial Management and Clinical Product Development of Pharmaceuticals and Medical devices; Medical Writing and targeted Market Investigations; Clinical Development (phase 1-4) within the Pharma area; PHC Pharma & Health Consulting: Medical reports, summaries or conclusions after evaluations of medically qualified information
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Pepgra is a Contract Research Organization (CRO) and provides consulting and services to life science companies in clinical research, Clinical Trial Monitoring, Patient Recruitment Services for Clinical Trials & Epidemiological Studies safety, Risk Management, Scientific Writing, Biometrics Services, and Regulatory affairs.
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We’re an independent pharmaceutical management consultancy that helps companies navigate processes involving pharmaceuticals approvals, clinical trials and medical writing.
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Metronomia is a specialized CRO for biostatistical consulting, biostatistical services and clinical data management in Munich (Germany).
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Smerud Medical Research is a European contract research organisation (CRO). We conduct clinical trials to advance new medical compounds, helping pharmaceutical and biotechnology companies with clinical project management, proof of concept and phase ii.
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At Project Data Sphere®, we believe in breaking down barriers to cancer clinical trial data sharing — barriers that historically have kept valuable trial data from ultimately benefitting the patients who so selflessly participate in them. By aggregating trial data from biopharmaceutical companies, academic medical centers, and government organizations and making it freely
Melissa J. Hogan: Author, Lawyer, Clinical Trials Consultant
Melissa J. Hogan is the co-author of Afraid of the Doctor: Every Parent's Guide to Preventing and Managing Medical Trauma (2021), as well as a lawyer and consultant on clinical trials.
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ClinicalAuditing.com, LLC provides international clinical Quality Assurance Auditing, Clinical Quality Management, and consulting services.
ClinicalAuditing.com, LLC provides international clinical Quality Assurance Auditing, Clinical Quality Management, and consulting services to the Pharmaceutical, Biotech and Medical Device industries in the area of Good Clinical Practice (GCP).
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Quretec provides web based Electronic Data Capture and Clinical Trial Data Management software and services - planning, database design, training, cleaning, medical coding and statistical analysis
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Homepage - Bio-Medical Research Design Ltd
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Evado Clinical - Evado
On-Demand Delivers the features of an enterprise as a simple on-demand service For more information Evado Clinical Fully mobile enabled integrated platform for collection and management clinical and device trials or studies data For more information Evado eConsent Stand-alone or integrated platform for electronic informed consent. For more information EvadoeCOA Collects patients clinical outcome assessments […]
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Welcome to GCP-Service International!StartA Full-Service Contract Research Organization Providing Clinical Trial Management SolutionsStart Voriger Nächster Making Clinical Trials accessible Founded in 2004, GCP-Service is a privately owned full-service Clinical Research Organization. Our company provides full-service management solutions for pharmaceutical and medical device clinical trials from phases I-IV. Our team consists of clinical experts from over […]
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PharmCMed is an independent life sciences consulting firm to support biopharmaceutical, medical device companies, service providers and the healthcare industry. Its specialty, core competence is to provide clients with the best services and solution in the areas of Research and Development (R&D), Clinical Operations, Procurement, (Outsourcing and Insourcing), Clinical Quality Assurance and healthcare industry.
Home - PharmCMed - BEST IN CLASS SUPPORT IN THE BIOPHARMACEUTICAL & HEALTHCARE INDUSTRIES
PharmCMed is an independent life sciences consulting firm to support biopharmaceutical, medical device companies, service providers and the healthcare industry. Its specialty, core competence is to provide clients with the best services and solution in the areas of Research and Development (R&D), Clinical Operations, Procurement, (Outsourcing and Insourcing), Clinical Quality Assurance and healthcare industry.
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Credevo is a global consulting organization specializing in regulatory, clinical development, licensing (out-/in-), and feasibility support for pharmaceuticals, nutraceuticals, medical devices, and biologics worldwide. Credevo facilitates global regulatory submissions, and cross-regional conduct of clinical development projects, particularly in Asia-Pacific and North America regions. Through innovative online platform, Credevo facilitates clinical trial feasibility with more than 100,000 investigators around the world.
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Medistat has been working with biotechnology and pharmaceutical companies for over 25 years, providing a wide variety of professional statistical and data management services for medical research(pharmaceutical and medical devices). Medistat is involved in development process from pre-clinical p
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One step forward | SPA Pharm
Spapharm s.r.o. is a small-sized virtual CRO legally founded in 2015. Through the virtual CRO, we help you to bring your project successfully towards its end by selecting the proper vendors. We manage and supervise clinical trials through a study adapted network of experts, local national freelancers or small companies, all working in several complementary roles according to the individual project and customer. All these measures ensure delivery of the project in time, in a high quality and on a smaller budget compared to large CROs.
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Global Product Development Strategy – Communication with Regulators & Payers. Discover how VCLS helps pharmaceutical, biotechnology and medical device companies on designing and implement innovative, efficient regulatory strategies, clinical trials, **** safety and vigilance management from pre-approval to post-approval activitiescommercialization.
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Home - Cedar Park Locksmith
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