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Dharma Bioconsulting

Dharma Bioconsulting is listed as a small consultant 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 consultant

Animal Science and Welfare Audits

  • Vendor Audits/Qualifications vendor audits for non-GLP and GLP nonclinical CROs throughout the US and Canada.

Clinical Consulting

  • Data & Risk Management Determine the extent of the risk and the reliability of the data used to access the aforementioned risk.
  • Regulatory Consulting Ensure that each product or device complies with all FDA rules and regulations.

Clinical Trials

  • Clinical Trial Design Develop study-related protocols, case report forms (CRFs) and database tools for records management.
  • 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.

Drug Development

  • 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.
  • Consulting Services Work with consultants who provide expert advice in various areas of research and technology.

Medical Communications

  • Quality Control/ Quality Assurance Documents Develop quality control or quality assurance documents.

Pharmacovigilance

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

REACH Services

  • Hazard, Exposure and Risk Assessment Evaluate the known hazard of a test compound in conjunction with the expected quantity and frequency of exposure.
Show all 14 services 2 more

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

  • Data and Text Mining Derive structured data from free text in order to become accessible for data-mining algorithms.

Source: Scientist.com supplier network

Where it operates

Sites by country, with the cities in each.

  • United States San Diego 1 site

Source: Scientist.com supplier network (site locations)

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Sources: Scientist.com supplier network.

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