The Insight Company Experience Regulatory Medical
Qualitative marketing research and consulting firmJapanese medical regulatory consultation
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Regulatory Medical Japanese Foreign Class Insight Qms Compliance Welfare Consultation Japan Boston Health Email Consulting Marketing And Advertising Strategic Pal Mhlw Medical Device Regulatory Submission Translation Interpreting
Reviews and Comments for The Insight Company
Feel free to add your comment or review!Best entries for Regulatory and Medical
1 Advanced Quality and Regulatory Medical
Medical device
Medical device regulatory affairs and quality system consultants with experience in FDA and CE regulations, pre-audits, and submissions.
Medical device regulatory affairs and quality system consultants with experience in FDA and CE regulations, pre-audits, and submissions.
2 pharmaceutical regulatory services
provides regulatory
provides regulatory support of various aspects of drug development, including clinical trials, marketed products, generics, otc products, medical devices, as well as regulatory activities related to mergers and acquisitions.
provides regulatory support of various aspects of drug development, including clinical trials, marketed products, generics, otc products, medical devices, as well as regulatory activities related to mergers and acquisitions.
3 Mediprotect - Regulatory Support
Offering regulatory
Offering regulatory support services to the Medical Devices Industry since 1996. Provides the services of Authorized Representative to medical device manufacturers throughout the world.
+ Parallels Parallelsreg Parallelsr Panel Automation Container Products Linux Virtualization Hosting Python Perl Domain Desktop Profitable Parallelsregdesktop
Offering regulatory support services to the Medical Devices Industry since 1996. Provides the services of Authorized Representative to medical device manufacturers throughout the world.
+ Parallels Parallelsreg Parallelsr Panel Automation Container Products Linux Virtualization Hosting Python Perl Domain Desktop Profitable Parallelsregdesktop
4 Bio-Reg Associates, Inc.
Regulatory consulting
Regulatory consulting firm assisting medical device, biologic, pharmaceutical, and biotech manufacturers meet US and international regulatory requirements.
Z Y
Regulatory consulting firm assisting medical device, biologic, pharmaceutical, and biotech manufacturers meet US and international regulatory requirements.
Z Y
5 Applied Regulatory Consulting
Applied Regulatory
Applied Regulatory Consulting Limited provides regulatory consultancy to the pharmaceutical industry, including strategic regulatory consultancy, project management, training, regulatory agency interactions and regulatory submissions.
Regulatory Consulting Applied Intelligence Contact European Terms Privacy Disclaimer Submissions Training Copyright Interactions Agency Europe
Applied Regulatory Consulting Limited provides regulatory consultancy to the pharmaceutical industry, including strategic regulatory consultancy, project management, training, regulatory agency interactions and regulatory submissions.
Regulatory Consulting Applied Intelligence Contact European Terms Privacy Disclaimer Submissions Training Copyright Interactions Agency Europe
6 Regulatory Bureau 'Cratia'
Consulting and
Consulting and active assistance in registration (regulatory affairs) and clinical trials of medicinal products, APIs, supplements, and medical devices in CIS countries (Ukraine, Russian Federation, Kazakhstan, Moldova, Byelorussia).
Consulting and active assistance in registration (regulatory affairs) and clinical trials of medicinal products, APIs, supplements, and medical devices in CIS countries (Ukraine, Russian Federation, Kazakhstan, Moldova, Byelorussia).
7 Biotech Consultant LLC
Biotech Consultant
Biotech Consultant LLC 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.
Biotech Consultant LLC 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.
8 Di Renzo Regulatory Affairs
Di Renzo
Di Renzo Regulatory Affairs is a pharmaceutical consultant aiding companies that need to register products (from medicines/dietary supplements and medical devices to cosmetics) at the AIFA and the Italian Ministry of Health.
Regulatory Affairs Di Renzo Medical Packaging Pharmaflash Gmp European Vast Aifa Foods Dietetics Joomlaprofessional
Di Renzo Regulatory Affairs is a pharmaceutical consultant aiding companies that need to register products (from medicines/dietary supplements and medical devices to cosmetics) at the AIFA and the Italian Ministry of Health.
Regulatory Affairs Di Renzo Medical Packaging Pharmaflash Gmp European Vast Aifa Foods Dietetics Joomlaprofessional
9 R. A. Q .A. Associates
R.A.Q.A. Associates
R.A.Q.A. Associates provides FDA and ISO related consulting services to medical device and pharmaceutical companies. We specialize in helping firms with regulatory and cGMP problems, constructing and implementing entirely new quality and regulatory systems or improving existing systems.
R.A.Q.A. Associates provides FDA and ISO related consulting services to medical device and pharmaceutical companies. We specialize in helping firms with regulatory and cGMP problems, constructing and implementing entirely new quality and regulatory systems or improving existing systems.
10 Precise Translations
Medical and
Medical and technical translation of patents, manuals, medical reports, insurance claims, journal articles, regulatory materials, and software and web localization.
Translations Interpretation Mexican Review Specialized Simultaneous Escort Cofepris Written Toll Free Contact Liability • Privacy Limitations Careers English Spanish
Medical and technical translation of patents, manuals, medical reports, insurance claims, journal articles, regulatory materials, and software and web localization.
Translations Interpretation Mexican Review Specialized Simultaneous Escort Cofepris Written Toll Free Contact Liability • Privacy Limitations Careers English Spanish
11 Medical Device Link
Offers medical
Offers medical manufacturers free information on industry suppliers, regulatory affairs, industry events, and job opportunities.
Offers medical manufacturers free information on industry suppliers, regulatory affairs, industry events, and job opportunities.
12 Medical Device Link
Offers medical
Offers medical manufacturers free information on industry suppliers, regulatory affairs, industry events, and job opportunities.
Offers medical manufacturers free information on industry suppliers, regulatory affairs, industry events, and job opportunities.
13 Medical Device Consultants, Inc. (MDCI)
provides worldwide
provides worldwide regulatory, clinical, and quality assurance consulting services to medical device and diagnostic product manufacturers to meet US, Canadian, and European requirements.
Medical Clinical Device Management Adaptive Monitoring Trials Design Addplan® Trial Services Project Data Study Software Contact Learn
provides worldwide regulatory, clinical, and quality assurance consulting services to medical device and diagnostic product manufacturers to meet US, Canadian, and European requirements.
Medical Clinical Device Management Adaptive Monitoring Trials Design Addplan® Trial Services Project Data Study Software Contact Learn
14 amarex clinical research
offers a
offers a full array of services to the pharmaceutical, biotech, medical device and medical diagnostic development industries. services include phase i through iv development planning, protocol development, clinical monitoring, data management, analysis, medical writing, and fda and other regulatory presentations.
Clinical Management Amarex Affairs News Research Regulatory Data Quality Medical Project Events Biostatistics Monitoring Consultancy Pharmaco Vigilance
offers a full array of services to the pharmaceutical, biotech, medical device and medical diagnostic development industries. services include phase i through iv development planning, protocol development, clinical monitoring, data management, analysis, medical writing, and fda and other regulatory presentations.
Clinical Management Amarex Affairs News Research Regulatory Data Quality Medical Project Events Biostatistics Monitoring Consultancy Pharmaco Vigilance
15 d-target
swiss clinical
swiss clinical research organization specializing in clinical research, regulatory services and medical marketing support for medical devices and in-vitro diagnostics.
swiss clinical research organization specializing in clinical research, regulatory services and medical marketing support for medical devices and in-vitro diagnostics.
16 enhesa
global ehs
global ehs compliance assurance. assisting multinational companies in ensuring ongoing ehs regulatory compliance. services cover some hundred countries and include: country profiles, regulatory monitoring, audit protocols, regulatory registers, and strategic corporate advice.
global ehs compliance assurance. assisting multinational companies in ensuring ongoing ehs regulatory compliance. services cover some hundred countries and include: country profiles, regulatory monitoring, audit protocols, regulatory registers, and strategic corporate advice.
17 medical & pharmaceutical information
mpi offers
mpi offers clinical research services within the ec as well as medical writing skills (ec-type clinical and pre-clinical expert reports as well as periodic safety update reports). we also provide ec-regulatory affairs assistance.
mpi offers clinical research services within the ec as well as medical writing skills (ec-type clinical and pre-clinical expert reports as well as periodic safety update reports). we also provide ec-regulatory affairs assistance.
18 Azary Technologies, LLC
Regulatory and
Regulatory and quality consulting for the medical device industry.
Regulatory and quality consulting for the medical device industry.
19 Palanquin Corporation Medical Writing Services
Firm provides
Firm provides writing services for medical education, marketing, research, and regulatory writing.
Firm provides writing services for medical education, marketing, research, and regulatory writing.
20 VTS Consultants, Inc.
Validation and
Validation and regulatory consulting services for the pharmaceutical, biotechnology, and medical device industries.
Validation and regulatory consulting services for the pharmaceutical, biotechnology, and medical device industries.
21 Smith and Associates
A consulting
A consulting firm specializing in regulatory affairs for medical device manufacturing.
A consulting firm specializing in regulatory affairs for medical device manufacturing.
22 MeddiQuest
Assists the
Assists the medical device industry by managing their international regulatory compliance activities
Assists the medical device industry by managing their international regulatory compliance activities
23 Medical Device Safety Service
European regulatory
European regulatory affairs company for ce mark and ISO services, an authorized european address, an authorized responsible person and authorized representative in the medical device industry.
European regulatory affairs company for ce mark and ISO services, an authorized european address, an authorized responsible person and authorized representative in the medical device industry.
24 Medical Device Safety Service
European regulatory
European regulatory affairs company for ce mark and ISO services, an authorized european address, an authorized responsible person and authorized representative in the medical device industry.
European regulatory affairs company for ce mark and ISO services, an authorized european address, an authorized responsible person and authorized representative in the medical device industry.
25 Promedica International
A global
A global provider of continuing medical education meetings and clinical regulatory services.
Clinical Research Services Good Management Organization Gcp Technology Contract Practice Cro Disclaimer Promedica Biostatistics Trial Careers Audits
A global provider of continuing medical education meetings and clinical regulatory services.
Clinical Research Services Good Management Organization Gcp Technology Contract Practice Cro Disclaimer Promedica Biostatistics Trial Careers Audits
26 Global Regulatory
Pharmaceutical, medical
Pharmaceutical, medical device, biotechnology, food, and nutraceutical consulting for the international markets.
Pharmaceutical, medical device, biotechnology, food, and nutraceutical consulting for the international markets.
27 FDC Services
A regulatory
A regulatory affairs and quality systems consulting company serving the medical device and pharmaceutical industries.
Services Regulatory Quality Systems * Mdr Fdc Consulting International Compliance Clinicalregulatory Furr Clinicalregulatoryaffairs Designplease Affairs Field Industries
A regulatory affairs and quality systems consulting company serving the medical device and pharmaceutical industries.
Services Regulatory Quality Systems * Mdr Fdc Consulting International Compliance Clinicalregulatory Furr Clinicalregulatoryaffairs Designplease Affairs Field Industries
28 Coastal Consulting Group, Ltd.
Medical device
Medical device regulatory affairs, clinical studies, quality systems, and documentation services.
Consulting Clinical Coastal Group Quality Technical Whats Medical Revised Deviceregulatory Document Cgmp Compatibility Services Gmp Controls
Medical device regulatory affairs, clinical studies, quality systems, and documentation services.
Consulting Clinical Coastal Group Quality Technical Whats Medical Revised Deviceregulatory Document Cgmp Compatibility Services Gmp Controls
29 PaxMed International,
Consulting services
Consulting services in medical devices - clinical trials, quality systems, regulatory submissions, biomaterials.
Paxmed Services People Consulting Contact International Company Reporting Powerful History Leaders Pages Device Welcome Events Navigation Medical
Consulting services in medical devices - clinical trials, quality systems, regulatory submissions, biomaterials.
Paxmed Services People Consulting Contact International Company Reporting Powerful History Leaders Pages Device Welcome Events Navigation Medical
30 Biologics Consulting Group- Regulatory Affairs Consultants for Manufacturers of biological products
Our staff
Our staff of consultants has over 200 years total 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.
Our staff of consultants has over 200 years total 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.
31 MDI Consultants
A quality
A quality assurance, regulatory, and clinical consulting firm providing services to the medical device, pharmaceutical and food industries.
Industry Fda News Mdi Compliance Services Medical Food Business Pharmaceutical Quality Consultants Testimonials Industries Device Iso Updates Consulting
A quality assurance, regulatory, and clinical consulting firm providing services to the medical device, pharmaceutical and food industries.
Industry Fda News Mdi Compliance Services Medical Food Business Pharmaceutical Quality Consultants Testimonials Industries Device Iso Updates Consulting
32 Medical Device Safety Service
A CE
A CE Mark, European regulatory affairs company for CE mark and ISO services, an authorized European address, an authorized responsible person and authorized representative in the medical device industry.
A CE Mark, European regulatory affairs company for CE mark and ISO services, an authorized European address, an authorized responsible person and authorized representative in the medical device industry.