NCGS, Incorporated is a full-service international CRO managing clinical trials since 1984 in drug, biologic, device, diagnostics and consumer products. NCGS provides full-service or strategic sourcing needs focused on risk mitigation. Contingency planning is actively employed, not just planned for. NCGS is a WBENC certified diversity supplier.
NCGS has supported the development or expanded labeling of 78 approved products and has ZERO 483s.
NCGS clinical teams are first in class, highly- tenured professionals
- 10+ years’ experience; A team remains throughout the trial
- Turnover rates are discernibly different at less than 3% annually
CLINICAL TRIAL THERAPEUTIC FOCUS INCLUDES:
- Neuro-Psych (CNS)
- Infectious Diseases / Critical Care
- Oncology, hematology, transplant
- Trials in multiple other areas have been conducted
ROBUST DIVISION OF COMPLIANCE & RECRUITMENT SPECIALIST
- CAPA initiatives
- Due diligence auditing
- Subject recruitment
- Call Center 24/7
- Trial Rescue
- Safety, SAE narratives and SAE reconciliation
FULL SERVICES INCLUDE:
• Clinical Operations and Monitoring
• Fully Integrated e-Based iCloud Systems
- e-REMOTE: Risk-based monitoring
- eTMF: TMF Migration, Consolidation
- ePAY: Grants, Contracts, Payments
- eDM: EDC, IWRS
- ePRO:Patient Reported Outcomes
- eCLIN: CTMS
• Medical Monitoring & Clinical Safety
• Quality Assurance & Regulatory Compliance
• Global Strategic Sourcing
• Medical Writing
WuXi AppTec provides a broad portfolio of R&D and manufacturing services that enable companies in the pharmaceutical, biotech and medical device industries worldwide to advance discoveries and deliver groundbreaking treatments to patients. As an innovation-driven and customer-focused company, WuXi AppTec helps our partners improve the productivity of advancing healthcare products through cost-effective and efficient solutions. With industry-leading capabilities such as R&D and manufacturing for small molecule drugs, cell and gene therapies, and testing for medical devices, WuXi AppTec’s open-access platform is enabling more than 4,100 collaborators from over 30 countries to improve the health of those in need – and to realize our vision that "every drug can be made and every disease can be treated."
Our vision is to conduct clinical trials better and more cost effectively than anyone else. We accomplish this by working with our clients to not only deliver the clinical trial effectively, on time and within budget, but also by leveraging our in-depth expertise to ensure the clinical trial is properly designed.
We believe there is increasing need for innovation, creativity and scientific expertise in clinical research, characteristics often synonymous with small Biopharma and hence, though we are proud to have a number of the world’s largest pharmaceutical companies as our clients, greater than 80% of our client portfolio is small Biopharma.
ACLIRES has performed trials for an international array of biotech companies as well as for some of the largest global pharmaceutical companies. With our broad access to patients and expertise, our aim is to rapidly initiate our client’s studies, even when a very special patient population is required.
Our services include:
- Early Phase Studies
- Late Phase Studies
- Regulatory Affairs
- Site Selection
- Scientific Services/Medical Writing
- Quality Management
Amarex is a global, full-service Contract Research Organization (CRO), whose leadership team has significant expertise conducting biomedical research, and whose combined experience includes the design and conduct of several hundred clinical research projects in many therapeutic indications. Amarex provides comprehensive services in Project Management (Phase I-IV, BE/BA, PK/PD), Regulatory Affairs (FDA Applications and meetings, Applications to International Health Authorities, GxP Compliance Audits), Clinical Operations, Adaptive Study Designs, Statistical Analysis, Data Management, Medical Monitoring, Safety and Pharmacovigilance, and General Consulting. Amarex can take your product through the entire approval process, from creating the regulatory approval strategy, to conducting trials, to writing the marketing approval application. Join our growing list of clients with approved products. Amarex provides high quality and cost efficient services.
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ClinChoice is a full-service clinical CRO dedicated to offering high-quality, efficient and flexible solutions to pharmaceutical, biotechnology, medical device, and consumer products clients worldwide. With a 25 year history of success, ClinChoice continues to be The Standard of Excellence for biostatistics, clinical operations, data management, statistical programming, CDISC, regulatory affairs, medical affairs and pharmacovigilance. ClinChoice has established major delivery centers across US, China, Europe, India, Japan and the Philippines. It has over 1,800 employees globally, with a strong and talented team, and a growing clinical operations presence in seven countries across Asia, North America and Europe.