Absolute Research Solutions was created to assist pharmaceutical companies in the successful and timely completion of their trials. Through over ten years of clinical trials experience, our consultants have been involved in all phases of the drug development process.
We understand that without qualified evaluable patients and quality data, your success will be impossible. We can assist in all phases of development...
Our multi specialty investigative site has extensive experience in both in and out patient protocols with a proven track record for success. Our study coordinators have conducted over 100 protocols and are continuously receiving training to stay up to date on all new regulations.
Our consultants can assist you in all phases of your project, from site selection to QA audits to project management to contract monitoring. Our experience and expertise speaks for itself. In this changing world of clinical trials it's good to have a resource who understands the logistics of running an investigative site in today's competitive market What it takes to strategically locate your patient population and to accurately execute the protocol.
Crown CRO is a privately owned Finnish CRO founded in 2005. Our headquarters are in Espoo, which is located in Finland’s capital city region. Crown CRO offices are located in Finland, Sweden, Denmark, Norway, Estonia, Latvia and Lithuania. We have ongoing trials managed by our employees in Netherlands, Belgium, UK, Iceland, Ukraine and Belarus. Rest of the Europe and USA we cover through our qualified CRO network.
Our services cover Phase I – IV clinical development from protocol design to final reporting or any parts of the trial in various business models. Data services, Regulatory consulting, Pharmacovigilance, QA, Study Rescue Services and Medical Translation services complete the service package.
Our key therapeutic areas include, but not limited to, CNS, Oncology, Endocrinology, Cardiovascular, Respiratory and Musculoskeletal. We also have strong recent experience in Medical Devices from various indications.
Our passion for research across all our in-house Full-Service functions provide effective and innovative solutions with seamless cooperation for Phase I-III trials in Europe offering special focus on Nordic-Baltic area, together with our own Global Data Services ensuring consistency regardless of where your trials are located, offer you unrivalled customer attention, flexibility and high local level expertise which are key assets you can count on.
While others are getting up to speed, DSP is getting results.
DSP Clinical is an award-winning, comprehensive CRO that delivers three distinct advantages — dedicated experts, straightforward pricing, and a perfect partnership. With a track record for getting drugs to market faster, DSP has managed more than 200 clinical trials in Phases I through IV across various therapeutic areas and has filed 24 regulatory submissions including NDAs, 510(k)s and PMAs.
Whether we are managing the entire study from start to finish or providing individual services, DSP’s global capabilities drive top-tier success for small to midsize pharmaceutical companies through unmatched experience, passionate leadership, aggressive strategies, and operational excellence.
We provide on-demand management and monitoring services that instantly scale to fit the size, complexity, and speed of your research study. Our extensive expertise covers a wide range of therapeutic areas that include reproductive endocrinology and infertility, urology, and gastrointestinal studies.
DSP takes a proactive, meticulous approach to customer studies and services. We understand customer needs and won’t settle for anything less than precision and accuracy for your clinical trial.
At DSP, we provide an effortless contracting process with fixed pricing, integrated budgeting, and no long-term contracts to simplify service delivery and minimize overhead. We identify and resolve potential study issues early and strategically allocate resources to ensure project completion on time and on budget. Our proven internal SOPs and QA metrics ensure that quality systems are in place and rigorously followed during every customer’s clinical study.
As a result of sustained company growth, we have ranked prominently on the Inc. 500/5000 list multiple times.
Founded in 2004, Pharmaron is a cutting-edge, fully integrated pharmaceutical R&D service platform supporting the life science industry. The company has invested in its people and facilities and established its comprehensive service offerings throughout the pharmaceutical R&D lifecycle. With operations in China, the US and the UK staffed by more than 11,000 employees, Pharmaron has an excellent track record in delivering end-to-end R&D solutions to its partners globally and enabling them to accelerate their novel drug discovery and development process.
Pharmaron is a contract research organization (CRO).
* Synthetic, medicinal and analytical chemistry services
* Biology services
* DMPK services
* Pharmacology services
* Drug safety assessment services
* Radiochemistry and isotopically labelled metabolism services
* Chemical & pharmaceutical development services
* Clinical development services
CRO - Contract Research Organization
Discovery Process Chemistry
Radiolabelled Chemical Synthesis
in vitro Biology
in vitro Screening
in vivo Pharmacology
Animal Disease Models
ex vivo Pharmacology
in vitro ADME
in vivo PK
Drug Product Manufacturing
14C / Carbon-14 Radiosynthesis
3H / Tritium Radiosynthesis
Microdosing Phase 0
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.