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Plus Project
Plus Project is listed as a small business research supplier in the Scientist.com network, with 1 site in 1 country.
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Sites
1
Countries
1
Services
What this research supplier says it provides, as listed in the Scientist.com network.
Type of company: Small business
Clinical Consulting
- Clinical Study Reporting (CSR) Report results of clinical trials to regulatory agencies. This includes participant flow, baseline characteristics, outcome measures, statistical analyses, and adverse events.
Clinical Trials
- Clinical Trial Design Develop study-related protocols, case report forms (CRFs) and database tools for records management.
- Statistical Analysis Planning Technical and detailed elaboration of the principal features of the analysis described in the protocol, and includes detailed procedures for executing the statistical analysis of the primary and secondary variables...
Data Science/Bioinformatics
- Biostatistical Design Use statistics to ensure appropriate pre-clinical and clinical study design.
- Clinical Biomarker Analysis An approach to finding markers that change in response to a drug or that identify a group that responds favorably to a specific therapy. These can be omics, molecular, histologic, radiologic, etc.
- Clinical Data Analysis Analysis that helps you make sense of your clinical data
- Clinical Data Science and Modeling A process that helps make sense of your clinical data
- Clinical Trial Integration Analysis The process of combining data from multiple clinical trials to understand categories of drugs and drug behavior in a more global way.
- Discovery Data Analysis Analysis that helps you make sense of your discovery data
Show all 7 in Data Science/Bioinformatics
- RWE/HEOR Market Analysis A process to understand how a drug is performing in the market and possible opportunities in the market
HEOR
- Health Economics and Outcomes Research (HEOR) Evaluate data collected during drug development to maximize the value of a therapeutic product.
Management Optimization & Development Strategies
- Big Data Computational assistance with analysis of large data sets to reveal patterns, trends and associations
Market Access
- Health Technology Assessment Submission (HTA Submission) Analyze the medical, social, ethical, humanistic, and economic considerations of a drug, medical device, or clinical procedures. Submissions are sent to regulatory agencies with different requirements that govern...
Show all 28 services
Medical Communications
- Abstracts Request services related to the writing and review of abstracts
- Data Visualization Visualize data collected from clinical trials and/or clinical research.
- Regulatory Submissions and Compliance Draft, format, and submit documents to Pharmaceutical approval agencies according to documentation and guidelines. This includes documents such as NDAs, INDs, SUSARs, AE reporting, RMPs, and PSURS.
- Review Article/ Submission Drafting and managing the process of submitting an objective, comprehensive summary of the current literature on a disease or treatment area to a peer-reviewed journal.
Old Category HEOR, RWE, Market Access
- Patient-Reported Outcome Studies Get self-reported information regarding the personal health status of an individual.
Pharmacovigilance
- Safety Data Management Safety data management involves the collection, analysis, and reporting of data related to the safety of a drug. Including preparing and submitting safety reports to regulatory authorities, which may include periodic...
Real World Evidence & Data
- Real-World Evidence Acquire clinical data from patients' medical records to analyze trends and the frequency of occurrence of different medical conditions.
- RWD - Oncology Data from oncology patients, can include clinical treatment, diagnosis, among others.
- RWD - Rare Diseases Data from patients with rare diseases, can include clinical treatment, diagnosis, among others.
- RWE/HEOR Data Analysis Analysis that helps you make sense of your RWE/HEOR data
Regulatory Affairs
- Regulatory Submission Documents Request services related to the submission and writing of New Drug Applications (NDA), Investigational New Drugs (INDs), and Investigator Brochures (IB) to the FDA and other regulatory bodies.
Scientific Data Services
- Bayesian Statistics Extract information from data sets that are subject to error or noise to see unobserved possibilities.
- Bioinformatics Bioinformatics is a powerful method of storing, retrieving and analyzing biological data.
- Data Quality Framework Manage data quality issues to maintain good quality data outputs.
- Scientific Data Visualization Exploration and reporting of data by means of graphs and plots.
- Website
- www.plus-project.co.uk
Where it operates
Sites by country, with the cities in each.
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United Kingdom 1 site
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