ACLIRES Bangkok Ltd.,

As one of the most experienced and leading CROs (Contract Research Organization) for over 35 years, McDougall delivers valuable insight to biotech and pharmaceutical clients across all phases of their clinical trials. With timely, accurate data and analytics, we help clients expedite their time-to-market and lower development costs.

McDougall Scientific specializes in Clinical Trial Design services, Statistical Analysis and Clinical Data Management. Known for delivering insights you can trust, we take the time necessary to understand your business requirements, align with your regulatory strategy, and mitigate risks to deliver a vital statistical strategy for the development of your product.

The result: a smooth, efficient, and trusted operation from start to finish. We welcome you to contact us whether you are a company with established assets, or an independent investigator exploring initiating an investigator trial.

Specialties:

Feasibility Assessment, Protocol Development, Study Startup, Project Management, Investigator Initiated Trials, Phase I-IV Trials, Clinical Data Management System, Statistical Services, EDC, Data Management, Supply Management, Randomization, Document Management, Clinical Trial Management, Site Monitoring, Medical Writing, Regulatory Services, Pharmacokinetics, Patient Recruitment,​ Pharmacovigilance, Safety Surveillance, Integrated Safety, Risk-based monitoring

VetPharm, Inc. is a full-service contract research organization (CRO) dedicated exclusively to animal health. It offers a complete menu of pilot/pivotal/post-marketing clinical trial support services, including protocol development, data form design, investigator recruitment, site qualification, enrollment enhancement, study administration, ICH-GCP training, site monitoring, data management, statistical analysis, medical writing, and regulatory support to pharmaceutical, biotechnical, nutraceutical, nutrition, and device companies in the United States and Europe. VetPharm employs a comprehensive study management system and a consortium of study-ready investigators which facilitate rapid study initiation, accelerated enrollment, and superior results to meet sponsors'​ critical timelines.

VetPharm has broad clinical trial experience across all therapeutic areas which enables it to undertake virtually any trial and complete it quickly, efficiently, and accurately. VetPharm's investigator consortium includes board-certified specialists in the following disciplines: Behavior, Cardiology, Dentistry, Dermatology, Endocrinology, Gastroenterology, Immunology, Internal Medicine, Neurology, Oncology, Ophthalmology, Radiology, Surgery, Theriogenology, and Urology.

Cromos Pharma is an international CRO with expertise in delivering all aspects of clinical trials in all clinical phases and a range of therapeutic areas.

Cromos Pharma offers fully integrated CRO services including regulatory consulting and compliance, project management; monitoring; medical writing; data management and biostatistics; drug and device registration services; logistics and warehousing; post-marketing services and independent audits. Cromos Pharma delivers rapid recruitment and excellent patient retention as well as expert study design and management.

Cromos Pharma's "No Patients - No Payments"​ initiative allows the sponsors to pay for performance and is our guarantee that the study timelines will be met.

Established in Moscow in 2004, Cromos Pharma has strong regional presences in Central and Eastern Europe, Russia and Post-Soviet Bloc countries. Its European HQ is situated in Dublin, Ireland and its US base is in Portland, Oregon.

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
- eTMF
- 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
• Biostatistics

Over 10 years ago, Peachtree was founded to fill a perceived missing principle in typical CRO services. Where can I find a CRO that will partner with me, understand my challenges, and solve issues to keep my program on track? Filling this need requires experienced clinical research professionals.

We focused on people – building an organization by investing in highly experienced personnel with broad therapeutic area expertise in a number of clinical trials. From single-center Phase I to global multi-center trials. Most all of our clinical personnel have both sponsor and CRO experience – allowing us
to fully understand the issues our sponsor-clients face. We built a rock-solid processes and systems infrastructure to support the teams and this investment continues today – always seeking to improve our service.

We also saw the opportunity to support an under-served segment of the market – emerging mid-sized companies. We felt they could benefit from access to highly-experienced teams that understand the challenges of limited resources and be flexible, reliable, and responsive. Most of all – provide solutions.

So where is Peachtree today?
? A full-service CRO offering project management, feasibility & subject recruitment, clinical site management & monitoring, data management, biostatistics, medical monitoring, medical writing, and
clinical quality assurance
? We are 80+ highly-experienced clinical research professionals with an average of more than 20 years relevant clinical experience
? Our client roster continues to grow having worked with nearly 100 pharmaceutical, biotech, and medical device companies providing full-service clinical trial support to niche services
? Continued investment in best-in-class systems such as IBM Clinical for EDC, Veeva Vault for eTMF, ZenQMS for quality management and training, and Oracle for CTMS.