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Research supplier
Parexel
Parexel is listed as a large business research supplier in the Scientist.com network, with 57 sites in 23 countries and 4 service areas.
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Sites
57
Countries
23
Services
What this research supplier says it provides, as listed in the Scientist.com network.
Type of company: Large business
Biomarkers
- Biomarker Clinical Validation Evaluate the predictive ability of a candidate biomarker for a disorder.
- Biomarker Services Evaluating normal/abnormal biological conditions and characteristics within the body
- Pharmacodynamic Biomarkers Discovery Identify candidate biomarkers indicative of the therapeutic outcome of a drug-target interaction.
- Predictive Biomarkers Discovery Identify candidate biomarkers suggestive of a response to a treatment.
Chemistry, Manufacturing and Controls (CMC)
- Drug Product Stability Use accelerated stress conditions to determine degradation pathways and identify manufacturing issues.
- GMP Synthesis Synthesize APIs including small molecules, formulations and protein-based drugs under GMP compliance.
Clinical Consulting
- Biomarker Services Consulting Expert advice to conduct solutions for evaluating normal/abnormal biological conditions and characteristics within the body.
- Biostatistics Consulting Apply statistical theory and mathematical principals to research
- Clinical Protocol Design & Development Creation of clinical protocol document which details how a clinical trial is designed, relating to to the methodology, hypothesis, and operation of clinical trial to ensure the safety of the patients is...
- Clinical Trial Recruitment Recruitment, enrollment and retention of patients for clinical trials.
- IND Writing Consulting Consulting for an Investigational New Drug Application
- Regulatory Compliance & Documentation Regulatory compliance describes the goal that organizations aspire to achieve in their efforts to ensure that they are aware of and take steps to comply with relevant laws, policies, and regulations.
Show all 9 in Clinical Consulting
- Regulatory Consulting Ensure that each product or device complies with all FDA rules and regulations.
- Study Budgeting Consulting Request for Consulting Services
- Support Staff Recruitment Recruit nurses, clinical staff, certified clinical research coordinators and research support staff.
Show all 70 services
Clinical Trials
- Bioequivalence Studies Assess the expected biological equivalence of two proprietary preparations of a drug.
- Clinical Research Services Determine the safety and effectiveness of medications and medical devices.
- Clinical Trial Design Develop study-related protocols, case report forms (CRFs) and database tools for records management.
- Consumer Healthcare Product Trials Conduct clinical research to ensure the safety and efficacy of consumer healthcare products used for oral care, skin care, nutrition, and hair care.
- Investigator Recruitment Enlist clinical research experts to assist in investigator selection, recruitment monitoring and database evaluation.
- Nutritional Trials and Studies Conduct clinical trials to test the efficacy and safety of food and dietary products.
Show all 13 in Clinical Trials
- Patient Recruitment Recruit and retain patients for clinical trials.
- Phase 1-3 Studies Design phase 1-3 studies that seek to identify if a drug is safe, effective, and more efficient than other available treatments on the market.
- Prospective Explorative Studies Conduct a prospective exploratory study to assess the safety and efficacy of a test drug during clinical trials.
- Regulatory Affairs Consulting Receive assistance ensuring compliance with regulatory requirements.
- Regulatory Operations Ensure that all specific regulatory documents are published and properly organized before submission.
- Site Monitoring Maintain oversight over participant's health during a clinical trial.
- Site Selection Select clinical trial sites with clinicians who recruit, enroll, treat and evaluate trial patients.
Creative
- Infographic Create a quick visual representation of information, data or knowledge.
Data Science/Bioinformatics
- Biostatistical Design Use statistics to ensure appropriate pre-clinical and clinical study design.
- Discovery Data Management A process that includes acquiring, validating, storing, protecting, and processing required data to ensure the accessibility, reliability, and timeliness of the data for its users.
Drug Development
- Bioinformatics Consulting Consulting Services for the science of collecting and analyzing complex biological data
- Small Molecule Drug Development Consulting Request consulting services related to small molecule development.
Food Safety & Regulations
- Dietary Exposure & Intake Assessments Estimate how much of a food chemical a population, or population sub-group, consumes.
HEOR
- Clinical Outcome Assessments (Non-Patient Reported) Measure a patient's symptoms, mental state and level of disease condition-related impact on daily life.
- Health Economics and Outcomes Research (HEOR) Evaluate data collected during drug development to maximize the value of a therapeutic product.
Human Biological Samples
- Human Breast Milk Acquire fresh/frozen normal breast milk based on patient demographics and history.
- Human Cerebral Spinal Fluid (CSF) Acquire fresh/frozen normal cerebrospinal fluid based on patient demographics and history.
- Human Plasma Acquire fresh/frozen human plasma
- Human Serum Acquire fresh/frozen normal serum based on patient demographics and history.
- Human Urine Acquire fresh/frozen normal urine based on patient demographics and history.
- Human Vaginal Fluid/ Swab Acquire fresh/frozen normal vaginal fluid based on patient demographics and history.
Show all 7 in Human Biological Samples
- Human Whole Blood Acquire fresh/frozen normal whole blood based on patient demographics and history.
Management Optimization & Development Strategies
- OECD Regulatory Development Consultation in safety testing, chemical notification and registry within OECD.
Market Access
- Market Access Materials Find general strategies and methods used to market a pharmaceutical product or device.
- Market Research & Business Intelligence Run market feasibility studies, establish customer needs, improve product performance and analyze competition.
- Marketing and Commercialization Identify, promote and prove the value of a particular drug to key stakeholders.
Medical Communications
- Medical Publications Make clear and accurate presentations of scientific and technical data.
- Medical Writing and Editing/Manuscript Development Communicate scientific, technical and health-related information to a range of audiences.
Medical/Commercial
- Life Cycle Assessment (LCA) Analyze the lifecycles of the products and services with regard to their environmental impacts.
Old Category HEOR, RWE, Market Access
- Non-Interventional Studies Examine different aspects of drug usage, including efficacy and safety, under real-life conditions.
- Patient-Reported Outcome Studies Get self-reported information regarding the personal health status of an individual.
Pharmacovigilance
- GxP Compliance Monitoring Ensure products or services adhere to a set minimum standard.
REACH Services
- REACH Services Assist in the registration, evaluation and authorization of chemical substances.
Real World Evidence & Data
- Clinical Phenotype Data Obtain phenotypic data and observations on patients such as the clinical manifestation of the disease, clinical and behavioral parameters, symptoms, and laboratory test results.
- Data Asset Validation Tools for validating that patient data and source has been accurately recorded.
- Data Merging Tools for combining various data sets into a single data set. Includes data consolidation.
- Real-World Data Acquire real-world data from patients' electronic medical records including clinical information generated during the course of healthcare.
- Real-World Evidence Acquire clinical data from patients' medical records to analyze trends and the frequency of occurrence of different medical conditions.
- Registries - Product Includes specific information about a product of interest, route of administration, dose, duration of use, start and stop date.
Show all 7 in Real World Evidence & Data
- Secondary Real World Evidence Analyze clinical trial data.
Regulatory Affairs
- Patient Risk Management Identify, contain, and manage risks related to patient safety.
- Post-authorization Safety Studies Research efforts conducted after a drug has been approved for market to monitor its safety profile in the general population. These studies aim to identify, characterize, or quantify potential adverse effects...
- Risk Evaluation & Mitigation Strategy (REMS) Evidence required by FDA to support the benefit of treatment outweighs the risks. Purpose of REMS is to prevent, monitor, and manage serious risk by informing, educating, and reinforcing actions to reduce frequency...
Safety Pharmacology
- Safety Pharmacology Assess the impact of a therapeutic for human use on vital organ systems before first-in-man drug testing.
Testing Services
- Stain Removal & Whitening Studies Assess the stain removal effectiveness of a tooth whitening product in healthy volunteers.
Other services
- IND Writing Receive assistance with materials for an IND application.
- NDA Writing Receive assistance in the NDA application process.
- New Request
- Observational Research Gain valuable insights into the association between a drug treatment and its outcomes such as long-term effectiveness and safety.
Service areas:
Biology
DMPK
Pharmacology
Clinical
Where it operates
Sites by country, with the cities in each.
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United States 24 sites
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United Kingdom 6 sites
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India 3 sites
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France 2 sites
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Italy 2 sites
Showing 5 of 23 countries.
About this supplier
In the supplier's own words, as listed in the Scientist.com network.
Parexel provides dose escalation, drug-drug interaction, biomarkers, first-in-man studies, ADME, imaging, and clinical research services.
- Website
- www.parexel.com
Work with Parexel on Scientist.com
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