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Novellas Healthcare

Novellas Healthcare is listed as a mid sized 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: Mid sized business

Chemistry, Manufacturing and Controls (CMC)

  • Clinical supply management Clinical supply management

Clinical Consulting

  • 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...
  • 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 Recruitment Recruitment, enrollment and retention of patients for clinical trials.

Clinical Trials

  • Case Report Monitoring & Auditing Ensure the adequate collection and traceability of clinical data in preparation for review by the FDA.
  • Clinical Biostatistical Services Analyze and interpret data throughout all phases of clinical trial development.
  • Clinical Project Management Management of clinical trial sites, as monitored by various clinical monitoring organizations. Ensure that the clinical trial is being performed according to the correct protocol to uphold the validity of the data...
  • Clinical Project Management Staffing Clinical project management staffing is the specialized recruitment, sourcing, and placement of qualified professionals
  • 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 34 in Clinical Trials 28 more
  • Clinical Trial Risk Management Plan that maintains treatment quality throughout lifecycle and improve decision making.
  • Contract CRA Services Flexible, outsourced monitoring and site management for clinical trials,
  • CTMS- Clinical Trial Management Systems A Clinical Trial Management System (CTMS) is a software platform used by pharmaceutical, biotech, and research organizations to plan, track, and manage the operational aspects of clinical trials
  • Decentralized Clinical Trial Enablement Decentralized Clinical Trial (DCT) Enablement refers to the strategic adoption, implementation, and utilization of digital technologies, local healthcare infrastructure, and logistical solutions to conduct clinical...
  • 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.
  • eTMF- Electronic Trial Master File Manage essential documents in compliance with regulatory standards
  • Functional Service Provision/Provider (FSP) Specialized outsourcing model in clinical research where a vendor supplies dedicated staff, technology, or processes to manage specific, discrete functions
  • Informed Consent Development Informed Consent is a prerequisite of any conduct within a clinical trial, and refers to the process in which the permission of the potential clinical trial subject is obtained. Informed consent applies to all...
  • Investigator Recruitment Enlist clinical research experts to assist in investigator selection, recruitment monitoring and database evaluation.
  • 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
  • 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.
  • Protocol Optimization via AI/ML Using of artificial intelligence and machine learning techniques to enhance and streamline experimental protocols or operational procedures for improved efficiency, accuracy, and outcomes.
  • QMS- Quality Management Systems Structured framework of processes, procedures, and responsibilities designed to achieve quality policies and objectives
  • 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.
  • 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 Budget Management Secure funding sources and manage contract negotiations for clinical trials.
  • Virtual Clinical Trial Monitoring Platform This digital research platform allows researchers to monitor their clinical trials remotely.
  • Wearables / Remote Patient Monitoring Source medical-grade or consumer-grade devices that track patients' vital signs and other health data remotely and wirelessly transmit this information to healthcare providers
Show all 50 services 38 more

Data Science/Bioinformatics

  • Clinical Data Analysis Analysis that helps you make sense of your clinical data
  • 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 Machine Learning/AI Complex analytical approaches to find patterns and make predictions in drug discovery projects

General in vivo Toxicology

  • Nonclinical Study Management Provide nonclinical study management services to pharmaceutical and biotech companies. The services can be customized to meet the clients needs.
  • Nonclinical Study Monitoring Provide nonclinical study monitors throughout the US and Canada to monitor in vivo and in vitro studies are CROs

HEOR

  • Clinical Outcome Assessments (Non-Patient Reported) Measure a patient's symptoms, mental state and level of disease condition-related impact on daily life.
  • Clinical Outcomes Measures patient's symptoms, mental, or physical effects of a disease or condition on how the patient functions, recorded by practitioner, provider, or instrument (not by patient).

Medical Communications

  • 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.

Pharmacovigilance

  • GxP Compliance Monitoring Ensure products or services adhere to a set minimum standard.

Source: Scientist.com supplier network

Where it operates

Sites by country, with the cities in each.

  • Belgium Ternat 1 site

Source: Scientist.com supplier network (site locations)

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Sources: Scientist.com supplier network.

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