Anabase International Corp

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
- Recruitment
- Regulatory Affairs
- Monitoring
- Site Selection
- Scientific Services/Medical Writing
- Consulting
- Quality Management

Our goal is to assist you to properly plan and execute your clinical strategy to assure early FDA approval and expedite your product to market.

Clinstat Consulting was founded in 1999 by Patricia Hamilton, RN, MS.

Patricia is a clinical expert with over 25 years experience. She is a Registered Nurse and holds a Master's Degree in Business Management. She has had extensive senior level technical and management experience delivering clinical research plans and studies on time and within budget for Fortune 500 global corporations as well as for small companies and start-ups. She has set up and managed clinical departments from the ground level and has hands on experience in all phases of developing a clinical/regulatory strategy, securing investigators, site selection, protocol development, site monitoring, generation of final reports and writing FDA submissions. Patricia and her staff are well suited to guide start-up companies or assist established firms with any or all your clinical needs.

Hoosier Cancer Research Network, Inc., formerly known as Hoosier Oncology Group, is an independent nonprofit contract research organization (CRO) that specializes in early phase multi-center, investigator-initiated oncology clinical trials. Our studies are conducted through a nationwide network of more than 450 academic and community sites. Our highly qualified team provides comprehensive study management including budgeting, contracting, LOI submission, study design, regulatory and IND support, custom EDC development and validation, safety reporting, monitoring, site management, correlative management, data management, and support for publication.

Hoosier Cancer Research Network’s vision and mission is to form unparalleled relationships between academic, community, pharmaceutical, and biotech collaborators with the goal of advancing cancer research, education, and patient advocacy.

Research Dynamics is a Clinical Research Organization (CRO) that provides high quality, flexible clinical trial services, GCP training, and consulting to the pharmaceutical, biotech, device industries as well as to investigators and academic medical centers. We use innovative technologies, experienced research professionals, and a commitment to clients through product development to approval.

As a full service CRO, we provide dedication, flexibility, value, and a unique depth of experience and expertise.
Complex trials or first trials in an emerging company require this depth of expertise and insight to ensure successful trial completion. Our strength is in our expericenced staff especially in clinical trial rescue studies where we can start work within 1-2 weeks. Our specialty is complex or difficult studies where our focused attention is needed.

As a focused CRO we concentrate on providing our clinical trial core competencies from site identification through trial conduct to final clean data collection. These activities include site monitoring, site management, project management, GCP auditing, regulatory document management and remote EDC monitoring.

As a full service CRO, we provide “best-in-class” experts for regulatory services, data management, statistics, pharmacovigilance, medical monitoring, etc. Our Clinical QA audit staff can conduct on-site clinical audits or internal audits such as report audits and documentation audits.

With the company’s training foundation, we continue to provide training in GCP and other research topics for any clinical research professional. We have written books on GCP for investigators, coordinators and monitors. Our templates for “SOPs for investigator sites” have been sold for over 15 yrs.

Our consulting services include assisting start-up companies with their clinical development plans, providing advice on clinical trials and process and system consulting.

Beaufort CRO (www.beaufortcro.com) is a global contract research organization (CRO) that provides in vitro diagnostic (IVD), medical device and biopharmaceutical companies with a full range of clinical, regulatory, quality and staffing solutions.

For over 15 years, we have earned a reputation for successfully helping sponsors get their products to market -- on time and on budget. Our depth of experience and proven track record means we can apply the highest level of expertise across every step of the process from project inception through regulatory submission. Most importantly, our dedicated and specialized teams develop solutions that truly reflect your unique project needs or gaps, including:
• Clinical Trial Services: Efficient trial management, site selection, monitoring, data management and biostatistics
• Regulatory Affairs: Result-focused regulatory strategies, protocol development, and pre- and post-market submissions and support
• Quality Solutions: Comprehensive on-site gap assessments, auditing support and remediation services
In addition to being one of the only CRO’s that is ISO 9001:2015 certified, Beaufort’s experience with hundreds of clinical trials and regulatory submissions helps ensure that you have a qualified partner by your side. Our teams are also experts in working across a wide range of platforms, therapeutic areas, regulatory pathways and technologies.

See how Beaufort CRO can accelerate your medical innovation -- and put our experience to work for you.
info@beaufortCRO.com
757-383-6000