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CROPHA
Belgium
A
1-10 Employees
-
Key takeaway
The company, Cropha, specializes in providing comprehensive clinical trial development services, including clinical monitoring and project management. With a focus on continuous improvement and expertise in various therapeutic areas, they ensure high-quality support for clinical investigations, particularly in the early phases.
Highlighted product
Service
Services - Cropha
CRO RELATED SERVICES Full or partial Clinical Trial Development Services (full service limited to phase I and II trials). Services include: Regulatory, Medical Writing, Drug Packaging/Labelling, Clinical Monitoring, Project Management, Data Management, Call Center for patient recruitment, Biostatistics, feasibility studies, notice readability studies, Pre- & Post CE-marking clinical investigations. PROJECTS Full or partial Clinical Trial […]
Transpharmation
Dublin, Ireland
A
11-50 Employees
2010
Key takeaway
Transpharmation is a prominent preclinical contract research organization (CRO) specializing in neuroscience, providing a range of robust animal models and expertise in drug development to deliver reliable and clinically relevant data essential for advancing preclinical programs.
Highlighted product
Core business
Preclinical Neuroscience CRO | Transpharmation
Transpharmation is a preclinical neuroscience CRO.
ClinPro Trials
San Francisco, United States
B
51-100 Employees
2010
Key takeaway
ClinPro Trials specializes in creating strategic clinical development plans and offers a range of consulting services, making it a valuable partner for biopharma firms.
Highlighted product
Service
Clinical Supply Services – ClinPro Trials
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Research Professionals Ltd
Budapest, Hungary
B
51-100 Employees
2014
Key takeaway
RP-CRO specializes in managing all phases of clinical studies, leveraging a network of experienced Principal Investigators to accelerate study enrollment. They offer comprehensive Study Start-Up Services, including feasibility, regulatory support, and protocol design, ensuring efficient and high-quality CRO services for pharmaceuticals and devices.
Highlighted product
Service
RP-CRO Study Start-Up Services | Research Professionals
Research Professionals CRO accelerates study start up with feasibility, regulatory support, biostatistics and protocol design, vendor/site selection, and contract management.
CROlife
Rome, Italy
B
11-50 Employees
-
Key takeaway
CROlife is dedicated to enhancing the clinical trial experience by providing innovative and tailored solutions throughout all phases of research, with a strong commitment to timely delivery and addressing specific challenges. Their expertise in clinical trials, regulatory affairs, and pharmacovigilance positions them as a reliable partner for clients seeking to navigate the complexities of the clinical research process.
Highlighted product
Core business
CROlife – Working together for progress
WORKING TOGETHER FOR PROGRESS Learn More Welcome to CROlife We are a team of passionate specialists delivering innovative, high quality, tailored clinical trial, regulatory and pharmacovigilance solutions. Send a message
ABX-CRO advanced pharmaceutical services Forschungsgesellschaft
Dresden, Germany
A
51-100 Employees
2002
Key takeaway
ABX-CRO specializes in preclinical studies, focusing on oncology and neuroscience, and has developed tools like IDAC-alpha® for dosimetry in alpha decay assessment. Their expertise in advanced pharmaceutical services ensures a strong foundation for preclinical proof of concept studies.
Highlighted product
Service
Preclinical | ABX-CRO advanced pharmaceutical services Forschungsgesellschaft mbH
Ora
Andover, United States
B
51-100 Employees
1985
Key takeaway
Ora has a dedicated Retina R&D team that focuses on clinical model and endpoint development, which is crucial for advancing research and supporting partners in the approval of products. Their expertise in designing and analyzing ophthalmic clinical trials enhances their capabilities in the preclinical stage.
Highlighted product
Service
CRO Services - Ora Clinical
PT. Prodia DiaCRO Laboratories (Prodia the CRO)
Special Region of Jakarta, Indonesia
D
11-50 Employees
2007
Key takeaway
Prodia the CRO is a prominent Indonesian contract research organization that offers a comprehensive range of services, including clinical trial solutions and site management. Their commitment to Good Clinical Practice ensures high-quality support throughout the research process.
Highlighted product
Service
Good Clinical Practice – Prodia the CRO
Invitek Inc.
Hayward, United States
B
1-10 Employees
2008
Key takeaway
Invitek Inc. offers a wide range of exceptional preclinical CRO services, including in-vivo and in-vitro models, tailored protocols, and a commitment to accelerated development. Their focus on high quality and responsiveness to client needs positions them as a valuable partner in drug discovery.
Highlighted product
Core business
Preclinical CRO Services | Empowering Research in Drug Discovery
Invitek Inc. offers wide range of Preclinical CRO Services, in-vivo and in-vitro models with Customized Protocols, Time Adherence, and Value.
CRC Pharma
Parsippany-Troy Hills, United States
B
11-50 Employees
2009
Key takeaway
CRC Pharma is a Clinical Research Organization (CRO) in New Jersey that specializes in supporting preclinical and clinical development programs. They offer a range of services including operational support, consulting, and expertise in regulatory affairs and pharmacokinetic analysis, all aimed at enhancing the development of new drugs and therapies.
Highlighted product
Core business
CRC Pharma
Technologies which have been searched by others and may be interesting for you:
Preclinical Contract Research Organizations (CROs) specialize in providing services that support the early stages of drug development. These organizations conduct preclinical studies, which are essential for assessing the safety and efficacy of new drugs before they enter clinical trials. They offer a range of services, including in vivo and in vitro testing, toxicology studies, pharmacokinetics, and data analysis. By collaborating with preclinical CROs, pharmaceutical and biotechnology companies can leverage expertise and resources, minimizing costs and timelines associated with drug development. These providers play a crucial role in generating the necessary data required for regulatory submissions, ultimately facilitating the transition from laboratory research to clinical applications.
Preclinical Contract Research Organizations (CROs) play a crucial role in drug development by providing specialized services that support the research and testing of new pharmaceuticals. They conduct a variety of preclinical studies, including pharmacokinetics, toxicology, and efficacy testing, which are essential for determining a drug's safety and effectiveness before it enters clinical trials. These organizations leverage advanced technologies and methodologies to streamline the preclinical phase, ensuring compliance with regulatory requirements. By offering expertise in study design and execution, preclinical CROs help pharmaceutical companies reduce time and costs associated with drug development, ultimately accelerating the journey from laboratory research to market readiness.
1. Drug Development Services
Preclinical CROs often provide comprehensive drug development services, including pharmacokinetics and pharmacodynamics studies. They assist in designing and executing experiments that evaluate the efficacy and safety of new compounds before clinical trials.
2. Toxicology Studies
Another essential service offered is toxicology studies. These assessments evaluate the potential adverse effects of new drugs on biological systems, ensuring that only safe candidates progress to human trials.
3. Biostatistics and Data Analysis
Preclinical CROs also typically offer biostatistical support and data analysis. This includes designing study protocols and analyzing the resulting data to ensure that the findings are robust and reliable for regulatory submissions.
4. Regulatory Support
Many preclinical CROs provide regulatory support services, guiding clients through the complex landscape of regulatory requirements. This includes preparing documentation and submissions needed for approval from health authorities.
5. Formulation Development
Formulation development is another critical service, allowing clients to create stable and effective drug formulations. This process often involves optimizing the drug delivery system to enhance bioavailability and therapeutic effectiveness.
When selecting a provider, it's essential to evaluate their experience and expertise in the specific therapeutic area relevant to your research. A proven track record in conducting preclinical studies similar to your project can offer valuable insights and enhance the likelihood of successful outcomes. Additionally, consider the technological capabilities and resources available at the CRO. Advanced facilities and access to cutting-edge methodologies can significantly impact the quality of data generated. Also, assess their regulatory compliance and quality assurance processes, as these factors are crucial in ensuring that your study adheres to industry standards and regulatory requirements.
Preclinical CROs (Contract Research Organizations) ensure regulatory compliance by adhering to guidelines set by regulatory bodies, such as the FDA and EMA. These organizations maintain Standard Operating Procedures (SOPs) that align with Good Laboratory Practices (GLP) to guarantee that all preclinical studies are conducted systematically and ethically. In addition, they employ trained professionals who stay updated on evolving regulations and industry standards. Regular audits and internal reviews are conducted to assess compliance, ensuring that data integrity and safety protocols are consistently upheld throughout the research process. This commitment to regulatory adherence not only protects the integrity of the studies but also facilitates smoother transitions to clinical trials.
Some interesting numbers and facts about your company results for Preclinical Cro
| Country with most fitting companies | United States |
| Amount of fitting manufacturers | 5540 |
| Amount of suitable service providers | 6923 |
| Average amount of employees | 11-50 |
| Oldest suiting company | 1985 |
| Youngest suiting company | 2014 |
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Some interesting questions that has been asked about the results you have just received for Preclinical Cro
What are related technologies to Preclinical Cro?
Based on our calculations related technologies to Preclinical Cro are Biomedical (Red), Bioinformatics (Gold), Environmental Biotechnology (Grey), Agricultural Biotechnology (Green), Food Related Biotechnology (Yellow)
Which industries are mostly working on Preclinical Cro?
The most represented industries which are working in Preclinical Cro are Healthcare, Other, Biotechnology, Pharmaceuticals, IT, Software and Services
How does ensun find these Preclinical Cro Companies?
ensun uses an advanced search and ranking system capable of sifting through millions of companies and hundreds of millions of products and services to identify suitable matches. This is achieved by leveraging cutting-edge technologies, including Artificial Intelligence.
