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Syneos Health

Syneos Health is listed as a large business research supplier in the Scientist.com network, with 3 sites in 2 countries and 3 service areas.

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Search companies, drugs, suppliers and investigators, and follow each one to the others. Individual plan, $249/seat/mo. Card required.

Sites 3

Countries 2

Type of company: Large business

Biomarkers

Biomarker Services Evaluating normal/abnormal biological conditions and characteristics within the body
Clinical Chemistry Measure analytes in serum, plasma, cells, tissue lysates or other biological materials.
Immunoassays Create antibody-based assays for the identification and quantification of specific antigens.
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.
Prognostic Biomarkers Discovery Identify candidate biomarkers representative of disease progression without treatment.

Biometrics

Specialty/Niche Labs Find providers covering a broad range of services that go beyond routine testing and analyses to support clinical trials.

Brand Communications

Patient-HCP Communication Aids Design and development of tools (visuals, guides, devices) that facilitate clear, accurate, and empathetic two-way dialogue between patients and their healthcare providers.

Chemistry, Manufacturing and Controls (CMC)

Chemistry, Manufacturing and Controls (CMC) Request Chemistry, Manufacturing and Controls services

Clinical Consulting

Bioanalysis Consulting Expert advice to properly and effectively discover, evaluate, and measure chemical or biological materials.
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
Cell Services Consulting Whether you are an experienced drug hunter working in the pharmaceutical industry or an academic researcher looking to submit g...
Clinical Development Planning Complex document that entails the entire clinical research strategy of a drug, describing the clinical studies that will be carried out for a pharmaceutical entity.
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...

Show all 17 in Clinical Consulting 11 more

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 Trial Consulting Consulting services for Clinical trials.
Clinical Trial Feasibility Request services related to Clinical Trial Design and feasibility.
Clinical Trial Recruitment Recruitment, enrollment and retention of patients for clinical trials.
Data & Risk Management Determine the extent of the risk and the reliability of the data used to access the aforementioned risk.
IND Writing Consulting Consulting for an Investigational New Drug Application
Orphan Disease Consulting FDA requires that an Investigational Review Board (IRB) must review all the documents related to the inclusion of participants within clinical trials. IRB is expected to review all the research documents...
Product Testing Consulting Expert advice to evaluate the effectiveness, quality, and legitimacy of a given item or good.
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.
Regulatory Consulting Ensure that each product or device complies with all FDA rules and regulations.
Support Staff Recruitment Recruit nurses, clinical staff, certified clinical research coordinators and research support staff.

Show all 189 services 174 more

Clinical Trials

Bioequivalence Studies Assess the expected biological equivalence of two proprietary preparations of a drug.
Case Report Monitoring & Auditing Ensure the adequate collection and traceability of clinical data in preparation for review by the FDA.
Central Institutional Review Board Services Ensure the safety and protection of human subjects participating in a study.
Clinical Lab Services Comprehensive testing, analysis, and research support for a medical study.
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.

Show all 45 in Clinical Trials 39 more

Clinical Trial Risk Management Plan that maintains treatment quality throughout lifecycle and improve decision making.
Comparator Drug Sourcing Streamline new drug development and clinical trials by comparing the efficacy of an experimental drug to a comparator drug.
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.
DCT Platform A digital environment designed to support and streamline decentralized clinical trials.
Diversity and Inclusion Consulting For Trials Diversity and inclusion consulting for trials involves providing expert guidance to ensure that clinical trials are designed and conducted in ways that include diverse populations and address barriers...
eCOA - Electronic Clinical Outcomes Assessments Use smartphones, computers and tablets to allow patients to directly report health outcomes.
eConsent - Electronic Informed Consent Monitor clinical trials through electronic informed consent given by patients.
ePRO - Electronic Patient-reported Outcome Patient reported outcome collected by electronic methods.
Investigator Meeting Planning & Execution Investigator planning and meetings ensure that there is proper communication and reliability during a clinical trial. Allows for efficient work flow.
Investigator Recruitment Enlist clinical research experts to assist in investigator selection, recruitment monitoring and database evaluation.
IP Import/ Export Licensing Receive assistance with intellectual property import and export licensing.
IP Labeling Proper IP labeling guidelines are produced by the Food and Drug Association. Based on the compound or product in need of proper labelling there are guidelines that can be followed.
IP Returns & Destruction Return the used and unused IP to the clinical trial sponsor for destruction, as well as send the used and unused IP for destruction in accordance with institution policy, or the standard operational procedure. Theses...
IP Shipments & Resupply IP shipments and resupply aid in the management of shipping of clinical trial material from warehouses to clinical sites, or vice versa. Shipping and resupply aids in restocking, drug orders, shipment tracking...
IP Storage IP storage protocols are specifically defined by the U.S. Pharmacopeia, Japanese Pharmacopeia, and the European Pharmacopeia that specifically define the proper storage and transportation conditions...
IRT Services IVRS and Drug supply services allow research conducting clinical trials to receive real time subject updates, drug supply and shipment tracking, and randomization for the clinical trial. These...
Mass Balance Studies Design a study to determine the mass balance of drug-related material occurring administration of dose, the ratio of parent drug metabolite(s) in circulation, and the primary route of excretion of drug-related material.
Nutraceuticals Clinical Research Trials Conduct clinical trials to test the efficacy and safety of nutraceuticals.
Patient Concierge Services Find a liaison between patients and healthcare providers, ensuring a smoother and more comfortable experience throughout the patient's journey.
Patient Recruitment Recruit and retain patients for clinical trials.
Patient Reimbursement and Travel Process individuals participating in clinical trials or receiving medical care are compensated for expenses related to travel, such as transportation, lodging, and meals
Pharmacokinetic Studies Design a study that observes the time course of drug absorption, distribution, metabolism, and excretion, as means to test the safety and effective therapeutic management of drugs in an individual patient.
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.
Post-Marketing (Phase 4) Studies Conduct phase 4 studies for confirming unrecognized safety issues, investigating possible hazards or establishing the expected safety profile of a veterinary medicinal product under market conditions.
Prospective Explorative Studies Conduct a prospective exploratory study to assess the safety and efficacy of a test drug during clinical trials.
Recruiting Healthy Volunteers Recruit volunteers who have no known significant health problems, and is willing and consenting to participate in research to test a new drug, device, or intervention.
Recruiting Special Populations Recruitment of volunteers who are categorized as part of a special population, or a protected part of the population such as the elderly, women, and children.
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. 
Remote Patient Monitoring Devices and Services Remote Patient Monitoring Devices and Services refer to technology and healthcare solutions that allow healthcare providers to monitor patients' health data and vital signs remotely, enabling real-time tracking...
Site Feasibility and Enrollment Modeling tools Site feasibility and enrollment modeling tools are analytical resources used to assess the viability of clinical trial sites and predict participant recruitment rates to optimize study design and execution.
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.
Site/Patient Payments Allow for different suppliers to organize the proper patient and site payments for a clinical trial. Provides real-time payments, reduce workloads for site staff and minimize the amount of time participants spend...
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...
Study/Site Feasibility Study Explore and test study practicality.
TeleHealth Delivery of healthcare services and information using electronic communication and information technologies, allowing for long-distance patient and clinician interactions
Telehealth Integration for Study Visits Telehealth integration for study visits involves using digital communication technologies to conduct clinical research visits remotely, allowing participants to engage with researchers from their own locations. This...
Virtual Clinical Trial Monitoring Platform This digital research platform allows researchers to monitor their clinical trials remotely.

Creative

Case Studies Recruit research participants with a behavioral condition to receive either an investigational behavioral intervention or a behavioral intervention in clinical use.

Data Science/Bioinformatics

Biostatistical Design Use statistics to ensure appropriate pre-clinical and clinical study design.
Clinical Data Management A process that includes acquiring, validating, storing, protecting, and processing required data to ensure the accessibility, reliability, and timeliness of the 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 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.
RWE/HEOR Data Management A process that includes acquiring, validating, storing, protecting, and processing required data to ensure the accessibility, reliability, and timeliness of the data.
Translational Data Management A process that includes acquiring, validating, storing, protecting, and processing required data to ensure the accessibility, reliability, and timeliness of the data.

Disease Models

Behavioral Testing Models Investigate sensory-motor and emotional functions, social behavior and day-night activity.
Diabetic Retinopathy Models Assess therapeutic efficacy of drug candidates in diabetic retinopathy models of disease.

Drug Development

Assay Development Consulting Request consultant services measuring the activity of a drug or biochemical in an organism or organic sample.
Chemistry, Manufacturing and Controls (CMC) Consulting Consultant services related to the development of pharmaceutical and biopharmaceutical drug products that are consistently effective, safe and high quality for consumers.
Safety Pharmacology Consulting Consulting services that help with the detection of potential undesirable pharmacodynamic effects of chemical entities on physiological functions.
Small Molecule Drug Development Consulting Request consulting services related to small molecule development.

General Marketing

Database Management Software Facilitate the collection, tracking and processing of biological facts, statistics and observations.

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.

In Vitro Assays

Cell Based Assays Consulting Expert advice to evaluate the functions of specific chemicals based on their constructions and systems.

In Vivo ADME

Absorption studies Study the factors determning how efficiently a compound may enter the bloodstream.

Management Optimization & Development Strategies

Big Data Computational assistance with analysis of large data sets to reveal patterns, trends and associations

Market Access

Academy of Managed Care Pharmacy (AMCP) Dossier Summary document that presents clinical, economic, and humanistic value of an intervention and associated disease state with the supporting evidence, formulated from the perspective of a particular stakeholder...
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.
Study Start Up Consulting Request for RWE/HEOR/Market Access Study Start Up Consulting

Medical Communications

Abstracts Request services related to the writing and review of abstracts
Adverse Events Reports Collecting, documenting, and forwarding reports of side effects or safety issues experienced by patients to the pharmacovigilance team for regulatory reporting.
Animated Content Development of diverse visual, interactive digital assets like infographics, data visualizations, and short animations to explain complex medical and scientific concepts simply.
Case Reviews Review medical cases from Clinical Trials.
Communication Plan Communications plan enables organizations and corporations to effectively deliver information to appropriate stakeholders and customers.
Competitive Intelligence Develop a coordinated competitive intelligence program which contains a systematic collection and analysis of information from multiple sources about a specific business's industry.

Show all 47 in Medical Communications 41 more

Consensus reports Develop and submit a report that is a comprehensive examination by an expert panel of a scientific or medical issue.
Data Visualization Visualize data collected from clinical trials and/or clinical research.
Delegate Logistics Managing the travel, accommodation, registration, and related administrative needs for attendees of investigator meetings, advisory boards, or congresses.
Distribution Strategy & Channel Recommendations Developing plans for how and where medical content (e.g., publications, training, MOA videos) will be efficiently delivered to the target healthcare audience.
Gap Analysis Compare the actual performance of an organization or corporation with potential or desired performance, as ways to effectively analyze resource management or allocation.
Investigational Medicinal Product Dossier (IMPD) and Investigational New Drug (IND) Dossier Develop and submit Investigational Medicinal Product Dossier (IMPD) and Investigational New Drug (IND) Dossier
KEE Identification, Mapping & Engagement Planning Systematic process to identify, categorize, and strategically plan outreach to Key External Experts (KEEs) based on their influence, specialization, and research activity.
KOL Engagement & Management Building and maintaining compliant, value-driven relationships with Key Opinion Leaders (KOLs) to collaborate on scientific exchange and clinical education initiatives.
Landscape Analysis Find a cohesive and consistent view of your main organization. Develop initiatives in analyzed areas of operations and analyze chosen key aspects of them.
Layperson Clinical Trial Result Dissemination Layperson clinical trial result dissemination involves translating complex clinical trial findings into clear, accessible language so that non-experts can easily understand the outcomes and implications.
Manuscript Co-Authorship and Publications Planning Manuscript co-authorship and publications planning involve collaborating among researchers to write, organize, and strategize the submission and publication of scientific findings in academic journals, ensuring proper...
Market & Competitor Analyses Evaluating the current therapeutic landscape, identifying unmet needs, and assessing the scientific positioning and data of competitor products.
Mechanism of Disease (MOD) & Mechanism of Action (MOA) Videos Production of dynamic, scientifically accurate animated videos illustrating how a disease develops (MOD) and how a drug therapeutically affects the body (MOA).
Medical Affairs Dossiers Develop medical affairs dossiers such as Global Value Dossiers or AMCP Dossiers.
Medical letters, Emails & Customized Responses Drafting accurate, balanced, and compliant answers to unsolicited scientific and medical inquiries from healthcare professionals or consumers.
Medical Literature Reviews Systematic searching, appraisal, and synthesis of published scientific literature to generate evidence-based reports on a specific topic, disease, or treatment.
Medical Publications Make clear and accurate presentations of scientific and technical data.
Medical Q&As Developing pre-approved, standardized documents containing accurate, balanced answers to anticipated scientific inquiries about a product or disease.
Medical Science Liaison (MSL) External Presentation Develop and design Medical Science Liaison External Presentations.
Medical Science Liaison (MSL) Support Support services for Medical Science Liaisons (MSL).
Medical Science Liasion (MSL) Training Training for medical science liaisons who want to work in pharmaceutical, biotechnology, medical device, and managed care companies.
Medical Writing and Editing/Manuscript Development Communicate scientific, technical and health-related information to a range of audiences.
Other Medical Affairs Videos Develop and design Medical Affair videos that are explainer videos and or augmented/virtual reality experiences.
Patient Narratives Compliant collection and use of individual patient stories to illustrate the impact of a disease or treatment, often for training or empathy-building purposes.
Payer Directed Communication Tools (other than Dossiers) Request services related to payer directed communication tools.
Pharmacodynamic/ Pharmacokinetic Reports Create Pharmacodynamic/ Pharmacokinetic reports to report to the appropriate regulatory bodies.
Poster Design and Development Design and Develop Posters for Poster Symposiums and conferences to effectively convey science information.
Poster Symposia, Summits, Product Theaters, etc. Support Comprehensive planning and execution support for organized, large-scale medical meetings and events used to present and discuss clinical data and research.
Protocol and Study Reports Write protocol and study reports, specifically relating to the drafting, writing, and editing of Clinical Safety Reports.
Publication Writing Create further publication documents. Investigational device exemptions (IDEs) BLAs, MAA, PMA, eCTDs, informed consents, CMC and manufacturing reports, orphan drug designations (ODD), briefing books.
Publications Plan Development & Management Strategic planning and oversight of all research dissemination activities, including outlining target journals, timelines, authors, and compliance for clinical data publications.
Quality Control/ Quality Assurance Documents Develop quality control or quality assurance documents.
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.
Sales Training Modules Develop and distribute sales training modules.
Sales Training Webinar Slide Decks Develop slide decks for sales training webinars.
Scientific Platform Develop a rigorous approach to creating a core story (grounded in the scientific literature) for a product. This involves identifying core concepts that address disease states, clinical needs, and product-related...
Scientific Training Solutions Developing comprehensive educational programs and materials to ensure internal teams, field medical staff, or external partners are fluent in the therapeutic area and product data.
Strategic Medical Communication Development & Planning High-level planning to define the core scientific messages and the tactical strategy needed to effectively convey clinical data to key stakeholders over time.
Target Product Profile (TPP) A sponsor prepared document which summarizes the drug development program that is described in terms of the labelling concepts. This profile is a communication method used between the FDA and sponsor which can be used...
Toxicology Reports Create pre-clinical toxicology reports.

Medical/Commercial

Health & Pharmacoeconomics Identify, measure and compare the cost-benefit ratio of products and services.

Model Development

Juvenile Toxicology Assess developmental and reproductive defects due to neurobehavioral, skeletal and muscle growth effects.

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

Adverse Event (AE) and Serious Adverse Event (SAE) Reporting Report unfavourable and unintended events (e.g.: abnormal laboratory results, symptoms or disease associated with treatments) to regulatory bodies via the FDA's Adverse Event Reporting System (FAERS) or other...
Aggregate Safety Data Review Cumulative summary of safety information regarding the collection, analysis, and submission of aggregated safety data to health authorities at specified intervals.
GxP Compliance Monitoring Ensure products or services adhere to a set minimum standard.
Local Pharmacovigilance Support in International Markets Connect with Pharmacovigilance professionals to uphold the National pharmacovigilance guidelines and regulations.
Periodic Safety Update Reports (PSURs) / Periodic Benefit-Risk Evaluation Reports (PBRERs) Preparation of safety reports to report adverse events that occurred during a specified time period. Evaluate if safety profile of treatment has changed since last report.
Pharmacovigilance Audits and Inspections Ensure companies meet their obligations to comply with pharmacovigilance guidelines and report adverse events. Some guidelines include: - having personnel, systems and facilities in place to meet their...

Show all 13 in Pharmacovigilance 7 more

Pharmacovigilance Case Processing Collect, synthesize, and report adverse events (AE) and adverse drug reactions (ADR) data to allow for successful data analysis, scientific assessment and decision-making based on the safety data associated...
Pharmacovigilance Literature Surveillance Conduct systematic and ongoing review of scientific and medical literature to identify new information about the safety profile of a drug. This process is crucial for detecting adverse drug reactions (ADRs) that may...
Pharmacovigilance Training and Education Training and education related to pharmacovigilance guidelines and adherence to EMA, FDA, and other regulatory bodies' documentation
Risk Management Plans (RMPs) Develop Risk Management plans (RMPs) that include information on a medicine's safety profile and plans for further pharmacovigilance activities designed to gain greater knowledge. These documents also explain how...
Safety Advisory Committees Collaborate with global experts to support safety surveillance monitoring and provide guidance on the safety of medicines and vaccines.
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...
Signal Detection and Management Capture pre-determined safety signals or indicators from a variety of sources to ensure the safety of the product post clinical trial. This includes the review of various sources such as ICSRs, EVDAs, FAERS, and other...

Product Development

Personal Care Product Development Services including the formulation, manufacturing, or designing of a personal/consumer care product or packaging.
Personal/Consumer Care Product or Service Request relating to the creation, testing or manufacturing of a personal care/consumer health/cosmetic product, ingredient or raw material.

Product Orders

Kits and Reagents Submit a request to multiple vendors for kits and reagents.

Protein Sciences

Protein Binding Determine drug-protein binding interactions
Protein Services Consulting Expert advice to evaluate and analyze protein function and expression.

REACH Services

Dossier Prep. and Consultancy Assistance with creation of a regulatory document that contains all the Clinical, non-clinical, and CMC information of a pharmaceutical product to be approved, registered, or marketed within a specific country.

Real World Evidence & Data

Pragmatic Clinical Trial Randomized trial comparing two or more treatments in a real world setting. The trial possesses minimal exclusion criteria and closely follows the procedures of the clinical practice in order to mirror clinical care...
RWD - Rare Diseases Data from patients with rare diseases, can include clinical treatment, diagnosis, among others.
RWE/HEOR/Market Access Safety Surveillance Monitor safety of treatment and determine methods to identify adverse events early
RWE/RWD Observational Research Research method for documenting clinical, economic, and or humanistic outcomes of actual medical practice absent the constraints of a more formal experimental design. See also Pragmatic Clinical Trials.
Secondary Real World Evidence Analyze clinical trial data.

Regulatory Affairs

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...
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.
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...

Regulatory Consulting

Toxicology Data Review Identify relevant toxicological endpoints for “No Observed (Adverse) Effect Level” (NO(A)EL) or “Lowest Observed (Adverse) Effect Level” (LO(A)EL).

Scientific Data Services

Bioinformatics Bioinformatics is a powerful method of storing, retrieving and analyzing biological data.
Data Infrastructure Design and deploy an information management solution suited to users' specific needs.
Data Quality Framework Manage data quality issues to maintain good quality data outputs.
Database Integration Convert bioinformatics results from multiple data sources (DSs) into a single operational format.
Large Language Models Use of Large Language models in target discovery, clinical trial design and development, analysis of clinical trial data and regulatory submissions. Services are tailored to the problem, specific context of biopharma.
Scientific Data Visualization Exploration and reporting of data by means of graphs and plots.

Show all 8 in Scientific Data Services 2 more

Scientific Pipeline Implementation Design, develop and deploy data analyses workflows.
System Development Plan, create and deploy an information system.

Testing Services

Consumer Care Testing and Substantiation Test personal care products using analytical, in vitro, and microbial test services
Safety In-Use Studies Safety-in-use studies assess the potential for a product to elicit adverse reactions under normal use conditions.

Other services

IND Writing Receive assistance with materials for an IND application.
NDA Writing Receive assistance in the NDA application process.
New Request  
Plain Language Summaries Request services related to the creation of plain language summaries.
Rare Diseases Recruitment of volunteers or study participants who have a rare disease, or specifically in the "U.S.when a chronic and enervating condition afflicts fewer than 200,000 people combined, and in the EU, when it affects...
Trial Awareness Create awareness about a clinical trial.

Service areas:

Biology DMPK Clinical

United States Morrisville, Princeton 2 sites
Canada Quebec 1 site

inVentiv Health, Clinical Division, a leader in drug development services, has a global infrastructure, therapeutic expertise, and commitment to quality that is unmatched in the industry. For pharmaceutical, biotechnology, generic drug, and medical device companies of all sizes around the world, inVentiv Health can help you transform promising ideas into commercial reality. inVentiv Health can conduct your Phase I – IIa clinical trials, quickly and efficiently in healthy and special populations. Our extensive database ensures rapid study participant recruitment and collaborations with world...

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inVentiv Health can conduct your Phase I – IIa clinical trials, quickly and efficiently in healthy and special populations. Our extensive database ensures rapid study participant recruitment and collaborations with world leading hospitals and research centers allows us to access to special populations to meet the needs of your program, from proof of concept and first in man, cardiac safety, to drug interaction study.

For Phase IIb – III clinical trials we offer a full range of services including biostatistics, data management, project management, study monitoring, patient recruitment, and global safety and pharmacovigilance. Our expertise in oncology, cardiology, neuroscience, infectious disease, and other therapeutic areas ensure that our project team professionally executes your program. Our exclusive access to UnitedHealth Care claims data allows you to have real-time, robust insight into the right patient populations and investigators. We will then consult with you to apply the data and develop a protocol for an efficient, safe and cost effective study.

Following approval, inVentiv Health Late Stage experts can guide you through the design and execution of a post-approval program, while addressing the needs and concerns of patients, providers, payers, and government regulators. We offer the vision and clarity to help you make smart and profitable decisions for your post-marketing programs with services including strategic and operational planning, observational studies and patient registries, health economics and outcomes research, safety/risk management and epidemiology, traditional interventional studies.

Whether you need a full service program, functional services, or signal expert, we offer one of the most experienced strategic partnering teams in the industry.

If functional services fit your strategy, inVentiv Health functional teams offer deep experience supporting a range of outsourcing models from a transaction involving a single project to broad based strategic partnerships. We currently have more than 30 active functional service partnerships (FSP).

If you need to supplement your team with qualified staff, we can support your clinical development program with a new way of handling a particular function while allowing you to maintain workforce direction with flexible staffing resources. inVentiv Health is experienced designing scalable services that have reduced our client's fixed costs, decreased the number of vendors that clients need to manage, and produced reliable data for their studies. We have a database with more than 200,000 candidates to rapidly staff programs with experience across a wide variety of therapeutic categories. Using a managed team can enhance the experience, freeing the client from day to day priority setting, progress assessments and management.

During your study, high quality and timely bioanalytical results are critical. inVentiv Health scientists have the expertise to solve the most complex bioanalytical problems, for small or large molecules, by developing and validating methods and using techniques from GC, GC/MS/MS, and LC/MS/MS to ELISAs, RIAs, immunoassays, and biomarkers. See our list of more than 1000 assays.
From preclinical to post-approval, we provide superior service to clients for both regulatory strategies and processes. We have assembled an exceptional team of former senior-level FDA officials, as well as other international regulatory and pharmaceutical consultants experienced in clinical development, planning and execution, and regulatory submissions.

For the applied knowledge, intelligent solutions, inVentiv Health is the product development partner that you can trust.

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Bioanalytical
Biomarker and Biosimilar List
Validated Assay List

Professional associations: BIOCOM
Website: syneoshealth.com

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