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Research supplier
Propharma Group
Propharma Group is listed as a large business research supplier in the Scientist.com network, with 2 sites in 1 country and 1 service area.
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Services
What this research supplier says it provides, as listed in the Scientist.com network.
Type of company: Large business
Chemistry, Manufacturing and Controls (CMC)
- Chemistry Manufacturing Controls Access contract manufacturing and regulatory guidance in setting specifications and drug dosage formulations.
Clinical Consulting
- 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
- 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.
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 Selection Select clinical trial sites with clinicians who recruit, enroll, treat and evaluate trial patients.
Data Science/Bioinformatics
- 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.
- Discovery Statistical and Mathematical Modeling Use mathematical variables and equations to establish relationships between data.
Drug Development
- Large Molecule Drug Development Consulting Develop large molecule drugs and complex biologics that have a therapeutic effect.
- Small Molecule Drug Development Consulting Request consulting services related to small molecule development.
Show all 21 services
Medical Communications
- 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.
- 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.
- Quality Control/ Quality Assurance Documents Develop quality control or quality assurance documents.
- 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...
Medical/Commercial
- Life Cycle Assessment (LCA) Analyze the lifecycles of the products and services with regard to their environmental impacts.
Regulatory Consulting
- Environmental Risk Assessment Conduct EU and US Environmental Assessment (ERA/EA) phases one and two according to VICH guidelines.
Other services
- IND Writing Receive assistance with materials for an IND application.
- NDA Writing Receive assistance in the NDA application process.
Service areas:
Where it operates
Sites by country, with the cities in each.
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United States 2 sites
About this supplier
In the supplier's own words, as listed in the Scientist.com network.
Propharma Group offers validation and compliance services for pharmaceuticals, biotechnology, and medical devices.
- Website
- www.propharmagroup.com
Work with Propharma Group on Scientist.com
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