Related categories 2
Sites 113
FDA compliance and regulatory consulting to help clients develop efficient and effective quality systems.
GMP consultancy in Canada, assisting global pharmaceutical, biological, medical device, natural health products, and cosmetics companies with manufacturing or regulatory compliance issues.
Drug development consultancy, based in the Washington DC area, focusing on preclinical toxicology, pharmacology, regulatory affairs issues, and U.S. Agent services to non-U.S. biopharmaceutical companies.
Consortium of pharmaceutical regulatory affairs consulting services.
Offers validation, ERP/CRM, testing, and enterprise efficiency services for medium and large scale organizations from Rockville, Maryland.
Medical device consultant providing manufacturers with market approval, clinical evaluation, FDA Clearance as well as evaluation from public health authorities. Offices in London, UK and Buenos Aires. Argentina.
Pharma regulatory affairs consultants based in New Delhi, India for the department of DCGI - Drugs Controller General of India - and NPPA - National Pharmaceutical Pricing Authority.
Provides compliance solutions for healthcare and financial sectors.
FDA regulatory experience and provide regulatory application support, "mock" FDA inspections, vendor and clinical trial site audits, statistical services, clinical trial design/review, and preparation of responses to FDA compliance actions.
Provides consulting services in the scientific and regulatory aspects of a wide range of medical devices and biologics with particular expertise in the areas of in vitro diagnostics (ELISA-based, PCR-based, SNPs, microarrays, pharmacogenomics, analyte specific reagent (ASR) regulatory compliance, and proteomics), medical device software (including bioinformatics), CPT coding reimbursement, and biotechnology-based products.
Providing a wide range of consulting services in GCP, GLP and GMP compliance.
Specialists in the field of pharmaceutical regulatory affairs.
EU regulatory affairs and preclinical/toxicological consulting.
Provide infrastructure to small to medium sized businesses in pharmaceutical, medical device, nutraceutical, pet, and cosmetic industries, including product development, project management, validation, quality, regulatory affairs, IT, sales, and marketing.
German consulting and engineering group with a focal on challenging capital investment projects in the Life Sciences industries.
CIEX Incorporated is dedicated to Quality Software and provides services in Software Lifecycle Processes, Software Quality Assessments, Reliable Software Design.
Document, drawing and spreadsheet management solutions for US FDA compliant pharma manufacturing units.
Offers full CRO services for medical devices manufacturers.
Medical device regulatory affairs, clinical studies, quality systems, and documentation services.
Regulatory compliance and validation documentation consulting for FDA-regulated drug manufacturing and testing companies worldwide.
Consulting firms specializing in supporting hospitals, physicians and attorneys address complex coding issues. Major emphasis on working with counsel in support of fraud and abuse allegations from third-party payers.
A commissioning, validation, cGMP, and regulatory compliance consulting services company.
Dedicated to providing the Life Science industry with solutions to complex regulatory and business critical requirements.
Software packages for quality assurance processes such as management of the documentation center, employee training records, environmental monitoring, deviations, CAPA, stability studies, and trends analysis.
Consultant involved with the development, purchase, installation, operation and maintenance of computerized systems used in FDA compliant applications.
European regulatory affairs consultancy providing specialist product development and registration services.
Services to the pharmaceutical industry, aimed at obtaining the appropriate authorizations in Italy and Europe.
German consulting firm assists pharmaceutical and healthcare companies with regulatory matters relating to drugs, medical products, nutritional supplements, biocides, and cosmetics.
Consultant for medical device importers, manufacturers, and physicians intending to introduce medical devices into U.S. commerce. Expert witness for neurological devices.
Draco Associates offers regulatory affairs consulting and quality assurance consulting and services for pharmaceuticals, natural health products, and other regulated products.
A suite of three integrated NeeS/eCTD software products for the creation, validation, viewing, manipulation and archiving of NeeS/eCTD submissions.
Regulatory affairs company with its HQ in Prague, Czech Republic assisting pharmaceutical and related industries with product registrations, GMP inspections, medical writing, clinical research/trials, bioequivalence studies. Regulatory services offered all EU languages.
Consultants to medical device companies for CE marking, authorized representative, FDA compliance and CCC mark for China. Offices in US, Europe and Asia.
Their employee development solutions provide for compliance management and learning management; their Gxp compliance Edition is "validation ready", ideal for GxP compliance training requirements in the pharmaceutical or medical device industries.
Specialized on eCTD submissions.
ISO 14971 risk management software system for compliance with ISO 14971:2007.
Professional network of regulatory affairs consultants and professionals.
Live broadcasting of FDA meetings via video-conferencing, webcasting and audio-conferencing. Post-meeting webcasts, DVD, CDs, videotapes and transcripts available.
A regulatory affairs and quality systems consulting company serving the medical device and pharmaceutical industries.
Consultant to the pharmaceutical industry in Germany and other European countries specialized in European drug registration procedures, CMC documents, CTAs, and product maintenance activities.
Regulatory consultants to the pharmaceutical and medical device industry in Australia and New Zealand.
Regulatory affairs services for the pharmaceutical, herbal, and biotech industries.
Online HIPAA training course and testing for healthcare professionals.
Online self paced HIPAA training and compliance do-it-yourself kits.
Provider of Quality and Compliance services to the Pharmaceutical / Biotechnology sector. Primarily assist organisations in the CSV field satisfy Regulatory and Compliance requirements. IVL has field knowledge in the implementation of compliance solutions.
FDA consultants based in Atlanta Georgia for the drug, biotechnology, biologics, and medical device industries.
IMI Consulting GmbH is specialized in advising and implementing: strategy development, global marketing, business development, licensing, and mergers and acquisitions.
Offering ISO 13485 and FDA QSR (21 CFR 820) Quality Manual and Operational Procedures and forms. Free software demo downloads available.
Regulatory consulting firm for international medical device companies interested in expanding their market penetration in Japan.
Provider of pharmaceutical development, regulatory and business intelligence information on the Japanese pharma and medical device market.
Specializes in assisting businesses with compliance of GMP/QSR regulations.
Quality and regulatory services to register medical devices in different markets. Supplier audits in Asia. Based in Korea.
Offers consultancy services to prevent and resolve compliance problems and to develop strategies for the submission and approval of drugs, biologics, and devices.
Provides pharmaceutical CMC regulatory consulting services, specializing in regulatory strategic, dossier preparation, and training services.
Lionpharm is an independent consultancy company providing all kind of regulatory affairs services covering the whole life-cycle of medicinal products in Europe.
Regulatory affairs eCTD software and service for electronic submission management for companies with USA FDA, Canada, Europe, EMEA, Japan PMDA agencies.
Helps life science companies analyze and improve the quality of their research laboratories and production environments, playing a focused role in the development and delivery of leading drugs and devices used to improve patients' lives.
European pharmaceutical/biotech consultancy specializing in project management, medical writing, and business development.
A quality assurance, regulatory, and clinical consulting firm providing services to the medical device, pharmaceutical and food industries.
Offer FDA compliant medical device standard operating procedures (SOP) for sale. Customization service is also available.
MEDIcept is a vertically integrated consulting firm specializing in contract engineering, quality assurance, and regulatory consulting.
Consulting and service company based in Switzerland, engaged in regulatory affairs of pharmaceuticals, medical devices, and in vitro diagnostics.
MundoMed is a consultancy based in Holland which specializes in CE-marking medical devices in Europe.
Assisting companies in the pharmaceutical, biotechnology, medical device, and diagnostic industries meet compliance and development needs.
NDA is a European regulatory affairs and patient safety consultancy.
A collaborative group of industry consultants serving the medical device and IVD industry.
Offers CE marking, US agent services to non-European medical devices manufacturers under AIMD, MDD, and IVD, under EU directives from Brussels, Belgium.
Provides quality and regulatory consulting and training for medical device and IVD manufacturers. Specializing in ISO 13485 and FDA QSR compliance, 510(k) submissions, form 483 and warning letter responses, CAPA programs, and CE mark approval.
Regulatory compliance solutions targeted for small-to-medium sized pharmaceutical companies.
Consulting group headquartered in Belgium. They manage biosafety and biotechnology compliance requirements.
Provides consulting services to pharmaceutical regulatory affairs professionals in the European Union.
Dr. Cheryl Blume and staff provide pharmaceutical and FDA regulatory consulting services including, but not limited to, development of pharmacovigilance assessment programs, pharmacokinetic protocols, non-clinical protocols and preparation for GCP/GLP and cGMP inspections.
Provide clinical and regulatory support of all phases of global drug development with operations in over 80 countries on all continents.
A fully integrated web-based eDMS and eCTD Submissions Solution Suite.
Pinney Associates brings science and public health expertise to pharmaceutical, consumer healthcare, and biologics clients in risk management, over-the-counter switch, and marketing strategy.
Validated labeling systems and inventory management software systems designed specifically for FDA 21 CFR Part 11 regulated environments.
EU authorized representative service in accordance with the EU medical device directive and EU machinery directive. Also act as FDA US agent for foreign establishments.
Specializing in CE marking, services for medical devices and also for manufacturers of personal protective equipment, in vitro diagnostics and medical test laboratories.
Provides CE marking, quality management system implementation and auditing of ISO 13485, (pre)clinical evaluation, product market approval (e.g. CE/EU and FDA/USA) and production registration as well as other regulatory services.
QFI is a European based consultancy providing CE marking services, EU Authorised Representative Programme, Microbiology Advisory Programme, QMS implementation, Conformity Assessment support and compliance audits
Provides consulting services to pharmaceutical, medical device, and life sciences industries in quality assurance, quality control, and regulatory affairs compliance.
Provides quality assurance documentation support. Assists in site licensing, product registration, HACCP development and implementation. Ottawa, Canada.
A management system for the risk analysis for producers of medical devices and in-vitro-diagnostics according to the world wide valid standard DIN EN ISO 14971.
Provides international regulatory solutions to the pharmaceutical and biologics industries.
RAA (regulatory affairs consultancy)
Italian consultancy providing regulatory affairs and business development services to pharmaceutical companies wishing to approach the Italian market or enlarge their existing business in Italy.
Provides strategic, technical, and regulatory consulting services to the pharmaceutical industry for drug, biologic, and device development.
Belgian company that provides consulting services in the fields of regulatory affairs, quality assurance, pricing and reimbursement, pharmacovigilance, and medical writing for medicinal products.
Specializing in the delivery of technical compliance and validation, QA knowledge, and GMP training solutions to the pharmaceutical, medical device and biotechnology industries.
Firm specializing in providing SAS training and expertise in working with clinical trials.
Supports biomedical research and medical device development by providing custom solutions.
Based in Singapore, providing healthcare consulting including regulatory affairs, quality management systems, marketing, and business development.
Works to get your equipment into production promptly while ensuring that all regulatory requirements are systematically fulfilled with a minimum of interference with operations.
A consulting firm specializing in regulatory affairs for medical device manufacturing.
Specializes in regulatory compliance consulting for biologics, medical devices and drug companies.
Provides HIPAA training courses in multiple formats both onsite and online.
Provides the pharmaceutical, biologics and medical device industries with regulatory and compliance information. Includes services provided, company news and events.
Engineering software suite covering risk management.
Located in Barcelona, Spain - helps manufacturers to obtain CE mark for their medical devices.
Thermal mapping and autoclave validation
The integration of services and software to provide competitive compliance, quality advocacy and thought leadership.
Provides consulting services in the scientific and regulatory aspects of a wide range of medical devices with particular expertise in the areas of in vitro diagnostics and biotechnology-based products.
Regulatory affairs consultancy in Poland and EU (MRP, DCP, national, medical devices, food supplements, and scientific dossier consultation).
A UK based company providing regulatory affairs consultancy and patient information leaflet user testing to the pharmaceutical industry.
Specializing in regulatory strategy development, preparation, and review of regulatory submissions.
Generic downloadable documents that are cGMP compliant.
Offers a full range of validation, compliance and technical services for the pharmaceutical, biotechnology and medical device industries.
They provide contract and consulting services in the following areas: validation and technical services (IQ OQ PQ protocols and validation master plans VMP), quality systems development, laboratory services, environmental monitoring, and water testing.
Worldwide validation, quality, compliance, and production services for the medical device, pharmaceutical, nutraceutical, and biotechnology industries.
Validation and regulatory consulting services for the pharmaceutical, biotechnology, and medical device industries.
Medical device regulatory affairs
Provides services to small and mid-sized pharmaceutical and device companies including biotechnology in the areas of preclinical, clinical, CMC and regulatory.
Provides consulting services in the areas of patent, regulatory affairs, marketing research, and QA/GMP documentation for small to medium size pharmaceutical companies.
Provides quality and regulatory consulting and training for medical device and IVD manufacturers. Specializing in ISO 13485 and FDA QSR compliance, 510(k) submissions, form 483 and warning letter responses, CAPA programs, and CE mark approval.
Assisting companies in the pharmaceutical, biotechnology, medical device, and diagnostic industries meet compliance and development needs.
Validated labeling systems and inventory management software systems designed specifically for FDA 21 CFR Part 11 regulated environments.
Offering ISO 13485 and FDA QSR (21 CFR 820) Quality Manual and Operational Procedures and forms. Free software demo downloads available.
Engineering software suite covering risk management.
Supports biomedical research and medical device development by providing custom solutions.
Provides services to small and mid-sized pharmaceutical and device companies including biotechnology in the areas of preclinical, clinical, CMC and regulatory.
A collaborative group of industry consultants serving the medical device and IVD industry.
Provides strategic, technical, and regulatory consulting services to the pharmaceutical industry for drug, biologic, and device development.
Specializes in regulatory compliance consulting for biologics, medical devices and drug companies.
Provides CE marking, quality management system implementation and auditing of ISO 13485, (pre)clinical evaluation, product market approval (e.g. CE/EU and FDA/USA) and production registration as well as other regulatory services.
Offers CE marking, US agent services to non-European medical devices manufacturers under AIMD, MDD, and IVD, under EU directives from Brussels, Belgium.
Offers a full range of validation, compliance and technical services for the pharmaceutical, biotechnology and medical device industries.
Italian consultancy providing regulatory affairs and business development services to pharmaceutical companies wishing to approach the Italian market or enlarge their existing business in Italy.
Pharma regulatory affairs consultants based in New Delhi, India for the department of DCGI - Drugs Controller General of India - and NPPA - National Pharmaceutical Pricing Authority.
A regulatory affairs and quality systems consulting company serving the medical device and pharmaceutical industries.
Provides compliance solutions for healthcare and financial sectors.
Specializing in the delivery of technical compliance and validation, QA knowledge, and GMP training solutions to the pharmaceutical, medical device and biotechnology industries.
Helps life science companies analyze and improve the quality of their research laboratories and production environments, playing a focused role in the development and delivery of leading drugs and devices used to improve patients' lives.
Their employee development solutions provide for compliance management and learning management; their Gxp compliance Edition is "validation ready", ideal for GxP compliance training requirements in the pharmaceutical or medical device industries.
Medical device regulatory affairs
Provides consulting services in the scientific and regulatory aspects of a wide range of medical devices and biologics with particular expertise in the areas of in vitro diagnostics (ELISA-based, PCR-based, SNPs, microarrays, pharmacogenomics, analyte specific reagent (ASR) regulatory compliance, and proteomics), medical device software (including bioinformatics), CPT coding reimbursement, and biotechnology-based products.
Works to get your equipment into production promptly while ensuring that all regulatory requirements are systematically fulfilled with a minimum of interference with operations.
Offers full CRO services for medical devices manufacturers.
They provide contract and consulting services in the following areas: validation and technical services (IQ OQ PQ protocols and validation master plans VMP), quality systems development, laboratory services, environmental monitoring, and water testing.
Services to the pharmaceutical industry, aimed at obtaining the appropriate authorizations in Italy and Europe.
Drug development consultancy, based in the Washington DC area, focusing on preclinical toxicology, pharmacology, regulatory affairs issues, and U.S. Agent services to non-U.S. biopharmaceutical companies.
Quality and regulatory services to register medical devices in different markets. Supplier audits in Asia. Based in Korea.
Belgian company that provides consulting services in the fields of regulatory affairs, quality assurance, pricing and reimbursement, pharmacovigilance, and medical writing for medicinal products.
A fully integrated web-based eDMS and eCTD Submissions Solution Suite.
Medical device consultant providing manufacturers with market approval, clinical evaluation, FDA Clearance as well as evaluation from public health authorities. Offices in London, UK and Buenos Aires. Argentina.
Online self paced HIPAA training and compliance do-it-yourself kits.
Regulatory compliance solutions targeted for small-to-medium sized pharmaceutical companies.
Based in Singapore, providing healthcare consulting including regulatory affairs, quality management systems, marketing, and business development.
Regulatory consulting firm for international medical device companies interested in expanding their market penetration in Japan.
Regulatory affairs company with its HQ in Prague, Czech Republic assisting pharmaceutical and related industries with product registrations, GMP inspections, medical writing, clinical research/trials, bioequivalence studies. Regulatory services offered all EU languages.
Consultant to the pharmaceutical industry in Germany and other European countries specialized in European drug registration procedures, CMC documents, CTAs, and product maintenance activities.
Offer FDA compliant medical device standard operating procedures (SOP) for sale. Customization service is also available.
Regulatory consultants to the pharmaceutical and medical device industry in Australia and New Zealand.
MundoMed is a consultancy based in Holland which specializes in CE-marking medical devices in Europe.
A commissioning, validation, cGMP, and regulatory compliance consulting services company.
ISO 14971 risk management software system for compliance with ISO 14971:2007.
German consulting firm assists pharmaceutical and healthcare companies with regulatory matters relating to drugs, medical products, nutritional supplements, biocides, and cosmetics.
Consortium of pharmaceutical regulatory affairs consulting services.
Consultant for medical device importers, manufacturers, and physicians intending to introduce medical devices into U.S. commerce. Expert witness for neurological devices.
FDA compliance and regulatory consulting to help clients develop efficient and effective quality systems.
Provides consulting services to pharmaceutical regulatory affairs professionals in the European Union.
Provides consulting services in the areas of patent, regulatory affairs, marketing research, and QA/GMP documentation for small to medium size pharmaceutical companies.
Professional network of regulatory affairs consultants and professionals.
Consultants to medical device companies for CE marking, authorized representative, FDA compliance and CCC mark for China. Offices in US, Europe and Asia.
Regulatory affairs consultancy in Poland and EU (MRP, DCP, national, medical devices, food supplements, and scientific dossier consultation).
FDA consultants based in Atlanta Georgia for the drug, biotechnology, biologics, and medical device industries.
German consulting and engineering group with a focal on challenging capital investment projects in the Life Sciences industries.
Offers consultancy services to prevent and resolve compliance problems and to develop strategies for the submission and approval of drugs, biologics, and devices.
EU regulatory affairs and preclinical/toxicological consulting.
Document, drawing and spreadsheet management solutions for US FDA compliant pharma manufacturing units.
Specializes in assisting businesses with compliance of GMP/QSR regulations.
Online HIPAA training course and testing for healthcare professionals.
A quality assurance, regulatory, and clinical consulting firm providing services to the medical device, pharmaceutical and food industries.
Consulting and service company based in Switzerland, engaged in regulatory affairs of pharmaceuticals, medical devices, and in vitro diagnostics.
Provides HIPAA training courses in multiple formats both onsite and online.
Specializing in CE marking, services for medical devices and also for manufacturers of personal protective equipment, in vitro diagnostics and medical test laboratories.
Provider of pharmaceutical development, regulatory and business intelligence information on the Japanese pharma and medical device market.
European pharmaceutical/biotech consultancy specializing in project management, medical writing, and business development.
Provides consulting services to pharmaceutical, medical device, and life sciences industries in quality assurance, quality control, and regulatory affairs compliance.
Specializing in regulatory strategy development, preparation, and review of regulatory submissions.
A suite of three integrated NeeS/eCTD software products for the creation, validation, viewing, manipulation and archiving of NeeS/eCTD submissions.
Live broadcasting of FDA meetings via video-conferencing, webcasting and audio-conferencing. Post-meeting webcasts, DVD, CDs, videotapes and transcripts available.
Thermal mapping and autoclave validation
Provide clinical and regulatory support of all phases of global drug development with operations in over 80 countries on all continents.
NDA is a European regulatory affairs and patient safety consultancy.
Regulatory affairs eCTD software and service for electronic submission management for companies with USA FDA, Canada, Europe, EMEA, Japan PMDA agencies.
Regulatory affairs services for the pharmaceutical, herbal, and biotech industries.
MEDIcept is a vertically integrated consulting firm specializing in contract engineering, quality assurance, and regulatory consulting.
European regulatory affairs consultancy providing specialist product development and registration services.
IMI Consulting GmbH is specialized in advising and implementing: strategy development, global marketing, business development, licensing, and mergers and acquisitions.
Firm specializing in providing SAS training and expertise in working with clinical trials.
Offers validation, ERP/CRM, testing, and enterprise efficiency services for medium and large scale organizations from Rockville, Maryland.
Consultant involved with the development, purchase, installation, operation and maintenance of computerized systems used in FDA compliant applications.
Specialized on eCTD submissions.
Provider of Quality and Compliance services to the Pharmaceutical / Biotechnology sector. Primarily assist organisations in the CSV field satisfy Regulatory and Compliance requirements. IVL has field knowledge in the implementation of compliance solutions.
Specialists in the field of pharmaceutical regulatory affairs.
Software packages for quality assurance processes such as management of the documentation center, employee training records, environmental monitoring, deviations, CAPA, stability studies, and trends analysis.
Dedicated to providing the Life Science industry with solutions to complex regulatory and business critical requirements.
FDA regulatory experience and provide regulatory application support, "mock" FDA inspections, vendor and clinical trial site audits, statistical services, clinical trial design/review, and preparation of responses to FDA compliance actions.
A management system for the risk analysis for producers of medical devices and in-vitro-diagnostics according to the world wide valid standard DIN EN ISO 14971.
Located in Barcelona, Spain - helps manufacturers to obtain CE mark for their medical devices.
Draco Associates offers regulatory affairs consulting and quality assurance consulting and services for pharmaceuticals, natural health products, and other regulated products.
Dr. Cheryl Blume and staff provide pharmaceutical and FDA regulatory consulting services including, but not limited to, development of pharmacovigilance assessment programs, pharmacokinetic protocols, non-clinical protocols and preparation for GCP/GLP and cGMP inspections.
A UK based company providing regulatory affairs consultancy and patient information leaflet user testing to the pharmaceutical industry.
Provides the pharmaceutical, biologics and medical device industries with regulatory and compliance information. Includes services provided, company news and events.
Provide infrastructure to small to medium sized businesses in pharmaceutical, medical device, nutraceutical, pet, and cosmetic industries, including product development, project management, validation, quality, regulatory affairs, IT, sales, and marketing.
Pinney Associates brings science and public health expertise to pharmaceutical, consumer healthcare, and biologics clients in risk management, over-the-counter switch, and marketing strategy.
Lionpharm is an independent consultancy company providing all kind of regulatory affairs services covering the whole life-cycle of medicinal products in Europe.
The integration of services and software to provide competitive compliance, quality advocacy and thought leadership.
Regulatory compliance and validation documentation consulting for FDA-regulated drug manufacturing and testing companies worldwide.
Provides quality assurance documentation support. Assists in site licensing, product registration, HACCP development and implementation. Ottawa, Canada.
EU authorized representative service in accordance with the EU medical device directive and EU machinery directive. Also act as FDA US agent for foreign establishments.
Validation and regulatory consulting services for the pharmaceutical, biotechnology, and medical device industries.
GMP consultancy in Canada, assisting global pharmaceutical, biological, medical device, natural health products, and cosmetics companies with manufacturing or regulatory compliance issues.
Generic downloadable documents that are cGMP compliant.
A consulting firm specializing in regulatory affairs for medical device manufacturing.
Consulting group headquartered in Belgium. They manage biosafety and biotechnology compliance requirements.
Medical device regulatory affairs, clinical studies, quality systems, and documentation services.
CIEX Incorporated is dedicated to Quality Software and provides services in Software Lifecycle Processes, Software Quality Assessments, Reliable Software Design.
Providing a wide range of consulting services in GCP, GLP and GMP compliance.
Worldwide validation, quality, compliance, and production services for the medical device, pharmaceutical, nutraceutical, and biotechnology industries.
QFI is a European based consultancy providing CE marking services, EU Authorised Representative Programme, Microbiology Advisory Programme, QMS implementation, Conformity Assessment support and compliance audits
RAA (regulatory affairs consultancy)
Provides consulting services in the scientific and regulatory aspects of a wide range of medical devices with particular expertise in the areas of in vitro diagnostics and biotechnology-based products.
Provides international regulatory solutions to the pharmaceutical and biologics industries.
Provides pharmaceutical CMC regulatory consulting services, specializing in regulatory strategic, dossier preparation, and training services.
Consulting firms specializing in supporting hospitals, physicians and attorneys address complex coding issues. Major emphasis on working with counsel in support of fraud and abuse allegations from third-party payers.
Last update:
October 2, 2023 at 5:35:17 UTC
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Regional: North America: United States: New Jersey: Localities: H: Hackensack: Health
- Recently edited by mcoupal
- Recently edited by mcoupal