Directory Help Search only in Regulatory AffairsSearch the Web

Regulatory Affairs

Business > Business Services > Consulting > Medical and Life Sciences > Regulatory Affairs

Go to Directory Home

Web Pages

View in Google PageRank order               Viewing in alphabetical order

21 CFR Consulting - http://www.21cfrconsulting.com/ Privately held virtual company in Encinitas, California, offering quality and risk assessments, remediation, IT system validation and training for FDA regulated industries.

Abnovo Ltd - http://www.abnovo.eu Specialize in regulatory consulting and authorized representation in the European Union.

Accurate Consultants - http://www.accuratefdaconsulting.com FDA compliance and regulatory consulting to help clients develop efficient and effective quality systems.

Acerna Inc. - http://www.acerna.ca GMP consultancy in Canada, assisting global pharmaceutical, biological, medical device, natural health products, and cosmetics companies with manufacturing or regulatory compliance issues.

Aexelar Regulatory Experts - http://www.aexelar.com Consortium of pharmaceutical regulatory affairs consulting services.

Aitheras, LLC. - http://www.aitheras.com/ Offers validation, ERP/CRM, testing, and enterprise efficiency services for medium and large scale organizations from Rockville, Maryland.

Al Weisenborn Medical Device Consulting - http://www.qsrhelp.com Regulatory affairs, quality assurance, custom software, and compliance contracting and consulting services.

Alenpharm - http://www.alenpharm.com Offering qualified services for the initial registration and re-certification of medical supplies, biologically active additives, and medications to sellers and manufacturers of these products.

Alphapharma Consulting - http://www.alphapharma.com/aboutus.html Good Manufacturing Practice (GMP) consulting services to the pharmaceutical industry.

American Technical Consultants - http://www.atccorp.net/ Consultant group specializing in providing services on FDA compliance issues to the food, drug and cosmetic industry.

Applied Regulatory Consulting - http://www.appliedregulatory.com Provides European regulatory consultancy to the pharmaceutical industry, including strategic regulatory consultancy, training, regulatory agency interactions, and regulatory submissions.

Arham Consultants.com - http://arhamconsultants.com 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.

Arvin Shroff Associates LLC - http://www.arvinshroff.com Advisor to pharmaceutical, biotechnology, medical device, food, dietary supplements, and legal companies.

ARx Pharma, Inc. - http://www.arxpharma.com/ Provide scientific and regulatory CMC consulting services to the global pharmaceutical and biopharmaceutical industry through strategic design and implementation of different aspects.

ASG Inc. - http://www.asg-inc.com Clinical Consulting: Specializing in regulatory affairs, sas programming, biotechnology careers, data management companies, staffing pharmaceutical, consulting, statistics, biotechnology, sas, and cro.

Atubra Inc. - http://atubra.com Atubra provides a full range of consulting services to FDA regulated industries including drug, medical device, cosmetic, and dietary supplement companies.

Azilon Corporation - http://azilon.com Provides compliance solutions for healthcare and financial sectors.

Barnhill & Associates, Inc. - http://barnhillassociates.net A specialty based consulting firm specializing in a range of scientific, laboratory, quality, and validation issues within the cGMP and GLP arena.

Biologics Consulting Group - http://www.biologicsconsulting.com 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.

Biotech Consultant LLC - http://www.biotech-consultant.com 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.

BNA consultants - http://www.gbnac.com Specialize in regulation of natural health products, health supplements, foods, pharmaceuticals, and cosmetics.

BrainWeaver, LLC - http://www.hipaatraining.com/ Online HIPAA training and compliance do-it-yourself kits.

Brandt Research Consulting LLC - http://www.brandtconsulting.us Providing a wide range of consulting services in GCP, GLP and GMP compliance.

Buphycon Consultancy - http://www.buphycon.com Provide scientific and regulatory affairs consultancy to investors, individual investigators, and the biopharmaceutical industry operating in the field of vaccinology.

Cabridge Regulatory Services - http://www.cambreg.co.uk Specialists in the field of pharmaceutical regulatory affairs.

CanReg Inc. - http://www.canreginc.com Regulatory specialists provide strategy, submissions, and support for global clients.

Carexa Inc. - http://www.carexa.com Consultants providing strategy and services for drug development and regulatory affairs.

CATS Consultants GmbH - http://www.catsconsultants.com EU regulatory affairs and preclinical/toxicological consulting.

Ceutical Labs - http://www.ceuticallabs.com 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.

Chemgineering - http://www.chemgineering.com German consulting and engineering group with a focal on challenging capital investment projects in the Life Sciences industries.

Chestnut Solutions Inc. - http://chestnutsolutions.com/ Offers global regulatory strategies, document management, electronic submissions and CTD filings to pharmaceutical and biotech companies and contract research organizations in Canada, Europe and the US.

CIEX, Incorporated - http://www.ciexinc.com CIEX Incorporated is dedicated to Quality Software and provides services in Software Lifecycle Processes, Software Quality Assessments, Reliable Software Design.

CIMCON Software, Inc. - http://www.part11solutions.com Document, drawing and spreadsheet management solutions for US FDA compliant pharma manufacturing units.

CL Tech Inc. - http://www.qualityleader.com Provide qualification, compliance, regulatory, training, and validation services to pharmaceutical, medical device, and biotechnology industries. Specializing in facility, equipment and Part 11 validations.

Clinical Device Group Inc. - http://www.clinicaldevice.com Clinical Device Group offers full CRO services for medical devices manufacturers.

CLINSTEP LLC - http://www.clinstep.com Multilingual regulatory affairs consultancy for medical devices, pharmaceuticals and diagnostic devices.

CMAC Consultancy - http://www.cmacusa.com Provides services like documentation and change control, validation and qualification execution, calibration and preventive maintenance, GXP training and implementation, project administration and commissioning, as well as, IT services/operation management.

Coastal Consulting Group, Ltd. - http://www.coastalcg.com Medical device regulatory affairs, clinical studies, quality systems, and documentation services.

Coda Corp. USA - http://www.codacorpusa.com/ Regulatory compliance and validation documentation consulting for FDA-regulated drug manufacturing and testing companies worldwide.

Coding Compliance Solutions - http://codingcompliance.com 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.

Compliance Associates - http://www.complianceassociates.ca Dedicated to providing the Life Science industry with solutions to complex regulatory and business critical requirements.

Compliance Control Ltd. - http://www.compliance-control.com Provide software products and consultancy expertise to help companies achieve compliant and validated systems.

ComplianceFDA, Inc. - http://www.complianceFDA.com/ FDA warning letter and CFR categorization and search database.

CompliaPharm, LLC - http://www.compliapharm.com Quality and regulatory compliance consulting services for the life sciences industry.

Computer System Validation - http://www.ComputerSystemValidation.com Consultant involved with the development, purchase, installation, operation and maintenance of computerized systems used in FDA compliant applications.

Creative Consultants - http://www.creativeconsultantsindia.com Mumbai (India) based agency providing regulatory dossier preparation, bioequivalence, clinical trial, and liaison services to Indian and international pharmaceutical companies.

Custom Business Development & Management Technology - http://www.cbdmt.com Assists companies in biotechnology, pharmaceutical and chemical markets with business development and market analysis.

Cyton Biosciences Ltd. - http://www.cyton.com European regulatory affairs consultancy providing specialist product development and registration services.

D & D Consulting LLC - http://www.ddcvalidation.com D & D Consulting LLC provides validation, commissioning, and quality services to the pharmaceutical, biotechnology, and medical device industries.

Delphi Consulting - http://www.delphiconsulting.com Delphi Consulting Group provides US FDA consulting services for medical devices.

Di Renzo Regulatory Affairs - http://www.direnzo.biz Provides regulatory services for human and veterinary medicines, mutual recognition, cosmetics, foods, medical devices, and translations. Rome, Italy.

Diapharm - http://www.diapharm.com German consulting firm assists pharmaceutical and healthcare companies with regulatory matters relating to drugs, medical products, nutritional supplements, biocides, and cosmetics.

Doctor Device - http://www.doctordevice.com/ Consultant for medical device importers, manufacturers, and physicians intending to introduce medical devices into U.S. commerce. Expert witness for neurological devices.

Draco Associates Ltd. - http://www.dracoassociates.com Draco Associates offers regulatory affairs consulting and quality assurance consulting and services for pharmaceuticals, natural health products, and other regulated products.

Drumbeat Dimensions Inc. - http://www.drumkey.com Professional compliance management company dedicated to developing products and tools for assessing, enhancing, and maintaining regulatory compliance.

DRW Research & Information Services, LLC - http://www.drw-research.com Provides regulatory affairs research and information for the healthcare industry.

eCTD Office - http://www.ectdoffice.com/ A suite of three integrated NeeS/eCTD software products for the creation, validation, viewing, manipulation and archiving of NeeS/eCTD submissions.

eCTDusergroup - http://www.ectd.it Italian professional community on e-ctd and e-submission topics.

Ehrreich Consulting, Inc. - http://www.regsolutions.com Regulatory consultants expediting FDA approval by solving tough scientific, clinical, and regulatory issues which may arise pre- and post-submission.

Emergo Group, Inc. - http://www.emergogroup.com Consultants to medical device companies for CE marking, authorized representative, FDA compliance and CCC mark for China. Offices in US, Europe and Asia.

Entrinsik - http://www.entrinsik.com Their employee development solutions provide for compliance management and learning management; our Gxp compliance Edition is "validation ready", ideal for GxP compliance training requirements in the pharmaceutical or medical device industries.

ERA Consulting Group - http://www.eraconsulting.com Specialist services for pharmaceutical companies in regulatory affairs, including the development/registration of biotechnology and biological medicinal products, with offices in Europe and the United States.

Estrin Consulting Group, Inc. - http://yourfdaconsultant.com/ ECG serves the medical device, pharmaceutical and cosmetic firms on FDA submissions, meetings and compliance related issues. Founder and President: Norman F. Estrin, Ph.D. Regulatory Affairs Certified.

Evolve Technologies, Inc - http://www.ehipaatraining.com Provide online privacy and security HIPAA training for business associates, employers, hospitals, clinics and health plans.

EZ Risk Management - http://www.EZRiskManagement.com ISO 14971 risk management software system for compliance with ISO 14971:2007.

FarmavitaR+ - http://www.farmavitar.com Professional network of regulatory affairs consultants and professionals.

FDA Compliance Solutions - http://www.fdacompliancesolutions.com Consultants providing a full range of FDA compliance services, including computer system validation, software validation, process validation, pharmaceutical validation and consulting.

FDALive.com - http://www.fdalive.com/ Live broadcasting of FDA meetings via video-conferencing, webcasting and audio-conferencing. Post-meeting webcasts, DVD, CDs, videotapes and transcripts available.

FDC Services, LLC - http://fdcservices.com A regulatory affairs and quality systems consulting company serving the medical device and pharmaceutical industries.

Fulcrum Pharma - http://www.fulcrumpharma.com/ European consultancy with experience in all aspects of regulatory affairs and pharmacovigilance.

Gamp Forum - http://www.gampforum.com Bio-Pharma professionals forum.

GCP Auditing Services - http://www.gcp-auditing.co.uk/ An independent consultancy providing auditing services for all aspects of clinical trials and good clinical practice.

GCP Solutions - http://mysite.verizon.net/sisbill1/gcp.htm GCP Solutions provides good clinical practice consulting services.

Global Quality Alliance, LLC - http://www.gqaconsulting.com Team of GMP consultants and quality auditors that provide consulting, auditing, and training to the pharmaceutical, biotechnology, API, dietary supplement, pharmaceutical compounding, and medical device industries.

Global Regulatory - http://www.globalregulatory.com/ Pharmaceutical, medical device, biotechnology, food, and nutraceutical consulting for the international markets.

Global Regulatory Services - http://www.globalregulatoryservices.com Regulatory affairs services for the pharmaceutical, herbal, and biotech industries.

GLP Quality Consulting, LLC - http://www.glpqualityconsulting.com Consulting services for the pharmaceutical, biotech, and agricultural chemistry industries.

GMP Online Consultancy - http://www.gmp-online-consultancy.com European-based, Good Manufacturing Practice (GMP) online consultancy.

GMP Quality Up - http://www.gmpqualityup.com Downloadable standard operating procedures and manuals on quality assurance, quality control management, process validation, microbiology testing, regulatory audits, manufacturing, warehouse, occupational health and safety.

GxP Medical Writing, LLC - http://gxpwriting.com/Home_Page.html A medical communications company for scientific/medical editing and writing services.

Harpaz Consulting Services - http://www.harpazconsulting.com/ Providing GMP compliance consultation, regulatory and technical expertise to manufacturers of drug products, active pharmaceutical ingredients, and medical devices worldwide.

HDM Corp. - http://www.hdmcorp.com Offers Internet-based HIPAA privacy and confidentiality training software for payers, providers and academia as well as HIPAA-compliant medical billing software for providers.

HIPAA Exams, Inc. - http://www.hipaaexams.com Online HIPAA training course and testing for healthcare professionals.

HIPAAdirect.com - http://www.hipaadirect.com/ A directory of HIPAA links.

http://abrimed.com - http://abrimed.com Regulatory affairs consultants for ISO, GMP, and FDA compliance

http://devicecompliance.com/ - http://devicecompliance.com/ Consultant and advocate for the medical device industry on issues of regulatory and standards compliance, risk management (ISO 14971) and general device safety.

http://mediqol.com - http://mediqol.com Offers a range of medical device consultancy services throughout Europe (including CE marking, regulatory and clinical trials management).

http://www.aclairo.com - http://www.aclairo.com Aclairo is a 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.

http://www.adneurope.com - http://www.adneurope.com Compliance for electronic record management for FDA regulated companies.

http://www.arx.com - http://www.arx.com 21 CFR Part 11 compliant digital and electronic signatures for any file format, document system, or web application.

http://www.bestechconsulting.biz - http://www.bestechconsulting.biz Consulting services guides medical companies through the FDA and CE compliance processes to ensure their business success. Provide solutions for regulatory compliance, product safety, litigation support and design and development of medical devices.

http://www.comply.co.il - http://www.comply.co.il 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.

http://www.cro.nu - http://www.cro.nu CRO in drug development process in close collaboration with the preclinical and clinical departments of pharmaceutical and biotech companies.

http://www.exalon.com - http://www.exalon.com Specialized on eCTD submissions.

http://www.isoxp.com/ - http://www.isoxp.com/ Offering ISO 13485 and FDA QSR (21 CFR 820) Quality Manual and Operational Procedures and forms. Free software demo downloads available.

http://www.ndareg.com - http://www.ndareg.com NDA is a European regulatory affairs and patient safety consultancy.

http://www.omsbar.com/ - http://www.omsbar.com/ OMSBAR provides consultancy services in regulatory affairs, product registrations, export certification, training, project management and product development, quality management, verification and validation, and maintains a core staff of experienced medical device personnel.

http://www.qarad.com - http://www.qarad.com Specializing in CE marking, services for medical devices and also for manufacturers of personal protective equipment, in vitro diagnostics and medical test laboratories.

http://www.qsitemed.com - http://www.qsitemed.com Qsite is a consulting group focused on the medical device industry. Services include advice on international regulatory affairs, clinical affairs, biostatistics, and global quality assurance.

http://www.quadras.de - http://www.quadras.de Service partner for international approval, registration, listing, and certification of medical devices in Europe, Asia, America, and Australia.

http://www.sagaem.it - http://www.sagaem.it Sagaem is an 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.

IDEC Validation Ltd - http://www.idecvalidation.com/ 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.

IHL Consulting Group, Inc. - http://www.ihlconsulting.com FDA consultants based in Atlanta Georgia for the drug, biotechnology, biologics, and medical device industries.

IMI Consulting GmbH - http://www.imiconsulting.com IMI Consulting GmbH is specialized in advising and implementing: strategy development, global marketing, business development, licensing, and mergers and acquisitions.

Independent Pharma Consultants - http://www.ipcons.co.uk Independent Pharma Consultants is a UK based regulatory affairs consultancy that offers a range of services.

Inflexxion, Inc. - http://www.navippro.com Turnkey solution for risk management needs that integrates sensitive surveillance with sophisticated signal detection, signal verification, and targeted prevention and intervention programs.

Infonetica - http://www.gcptraining.org.uk GCP online training course provides a comprehensive guide to the basic principles, regulations, and guidelines of ICH good clinical practice.

Innovative Automation - http://www.21cfrpart11compliance.com/ Part 11 compliance software solutions designed for MS-Excel, MS-Word, electronic laboratory notebook, and file replication.

Innovative Consultancy Services - http://www.pharmaceutical-consultancy.com Indian pharmaceutical consultant company providing services in regulatory affairs, pharmaceutical dossiers, product/process development, and validation services.

International Regulatory Business Consultants, L.L.C. - http://irb-c.com Providing scientific and regulatory consultant services to the global pharmaceutical, nutritional supplement, medical device, and diagnostic product industries

IPMB GmbH - http://www.ipmb.eu/ Institute for regulatory affairs and pharmaceutical services located in Germany.

ISOComp, Inc. - http://www.isocomp.com/ ISOtrain software distributors and consultants to bring training processes into FDA compliance and provide general consulting for pharmaceutical and biotechnology companies.

Jim Colyn & Associates Quality Consultants, LLC - http://www.jcolynconsulting.com Consulting services targeting compliance and performance for human tissue processors, tissue recovery organizations, organ procurement organizations, eye banks, reproductive banks, and medical device manufacturers.

Joe Schwoebel, BSEE, MBA - http://www.schwoebel.net Offers consulting services related to product planning, clinical study, regulatory affairs and reimbursement strategy. Includes resume, certifications and press releases, and FDA approvals.

Jouhou Koukai Services LLC - http://www.jouhoukoukai.com Provider of pharmaceutical development, regulatory and business intelligence information on the Japanese pharma and medical device market.

Kamm & Associates - http://www.fda-consultant.com Specializes in assisting businesses with compliance of GMP/QSR regulations.

Karandikar Laboratories Pvt. Ltd. - http://www.laboratorytestingindia.com Test and calibration laboratory located in India.

Karlton CMC Consulting - http://www.karltoncmcregulatory.net Specializing in pharmaceutical CMC regulatory affairs providing long range strategic planning, technical writing, and in-house regulatory affairs training.

Kemic Bioresearch - http://www.kemic.com Kemic Bioresearch provides consulting, research and training in the pharmaceutical sciences (pharmacokinetics, pharmacology and toxicology).

Kennedy Writing Service (KWS) - http://www.kennedywritingservice.com Medical writing and proofreading company.

Kobridge Consulting Ltd - http://www.kobridgeconsulting.com Korean consultants to medical device companies for CE marking, Canadian approvals, and FDA compliance.

KRM Associates - http://www.krm-associates.com/ Regulatory due diligence advisory practice for the health care industry specialized in domestic & international regulatory requirements for medical products (e.g. medical devices, pharmaceutical, tissue products, and in vitro diagnostics).

Lachman Consultants - http://www.lachmanconsultants.com Offers consultancy services to prevent and resolve compliance problems and to develop strategies for the submission and approval of drugs, biologics, and devices.

Leonard T. Flynn - http://www.drflynnconsulting.com An independent regulatory and scientific consultant who provides assistance to pharmaceutical, health product and chemical manufacturers for them to meet the requirements of government agencies.

Lewis CMC Consulting - http://www.lewiscmc.com Provides pharmaceutical CMC regulatory consulting services, specializing in regulatory strategic, dossier preparation, and training services.

Lionpharm Regulatory Consulting GmbH - http://www.lionpharm.com Lionpharm is an independent consultancy company providing all kind of regulatory affairs services covering the whole life-cycle of medicinal products in Europe.

Lorenz LIfe Sciences - http://www.lorenz.cc Regulatory affairs eCTD software and service for electronic submission management for companies with USA FDA, Canada, Europe, EMEA, Japan PMDA agencies.

Mandell Horwitz Consultants LLC - http://mandellhorwitzconsulting.com Regulatory and scientific consulting for medical devices and other FDA-regulated products.

MarcM Consulting Canada - http://www.marcmconsulting.ca Regulatory affairs consultants assisting pharmaceutical and related industries with product registrations, GMP inspections, ISO conformity, clinical research/trials, bioequivalence studies, and DMF preparations. Regulatory and business development services offered in English, Portuguese, and Spanish.

Marion Weinreb and Associates, Inc. - http://gmpsrus.com Assisting companies in the pharmaceutical, biotechnology, medical device, and diagnostic industries meet compliance and development needs.

Masy Systems - http://www.masy.com/ Validation and calibration services for the pharmaceutical, biotech, and related fields. Information on equipment and shipper studies.

MDI Consultants. Inc. - http://www.mdiconsultants.com/ A quality assurance, regulatory, and clinical consulting firm providing services to the medical device, pharmaceutical and food industries.

Med Pharma Solutions, LLC - http://medpharmasolutions.com/ Provides on-site compliance consulting services including factory acceptance testing, commissioning, IQ/OQ/PQ's, validation and qualification services to the FDA regulated industries.

Medcon Taiwan, Inc. - http://www.medcon-taiwan.com A Taiwan-based regulatory affairs consultant to the medical and life science industry

Medical Device Consultants - http://www.medicaldeviceconsultants.ca Located in the Toronto, Ontario (Canada) region.

Medical Device Consultants, Inc. (MDCI) - http://www.mdci.com Provides worldwide regulatory, clinical, and quality assurance consulting services to medical device and diagnostic product manufacturers to meet US, Canadian, and European requirements.

MEDIcept - http://www.medicept.com MEDIcept is a vertically integrated consulting firm specializing in contract engineering, quality assurance, and regulatory consulting.

Medius AG - http://www.medius-ag.ch Consulting and service company based in Switzerland, engaged in regulatory affairs of pharmaceuticals, medical devices, and in vitro diagnostics.

NJK & Associates, Inc. - http://njkconsulting.com NJK & Associates are a collaborative group of industry consultants serving the medical device and IVD industry.

Obelis European Authorized Representative Center - http://www.obelis.net/ Offers CE marking, US agent services to non-European medical devices manufacturers under AIMD, MDD, and IVD, under EU directives from Brussels, Belgium.

Octagon Research Solutions, Inc. - http://www.octagonresearch.com Offers a suite of services that span the entire clinical research and development lifecycle.

Online GCP Training - http://www.onlinegcp.com Online good clinical practice training.

Oracle Consulting Group - http://www.fdamaze.com Consultants for FDA and internationally regulated medical device firms, specializing in submissions, compliance, warning letter responses, inspection responses, quality system compliance, auditing and training

PAT toolkit - http://www.pattoolkit.com Provides information on the FDA’s Process Analytical Technology (PAT) Initiative and outlines a software package to help pharmaceutical manufacturers implement this initiative.

Paul Regulatory Services Limited - http://www.paulrs.co.uk A regulatory affairs consultancy based in the UK.

Perfect Consultants - http://www.perfect-consultants.com Association of consultants engaged in providing regulatory support to Pharmaceutical and Active Pharma Ingredients (API) industries.

Perkins and Perkins - http://www.perkinsandperkins.net FDA consultants Perkins and Perkins, Inc. conduct mock FDA audits to insure Good Clinical Practice (GCP) compliance, quality assurance and FDA audit preparation.

Perseus Partners - http://www.perseus.be Consulting group headquartered in Belgium. They manage biosafety and biotechnology compliance requirements.

PH PharmAnalysis GmbH - http://www.pharmanalysis.de Consultancy based in Germany that offers scientific and regulatory services for the pharmaceutical industry.

Pharma-EU s.r.o. - http://www.pharma-eu.com Provides consulting services to pharmaceutical regulatory affairs professionals in the European Union.

Pharmaceutical Development Group - http://www.pharmdevgroup.com 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.

Pharmaceutical registration in EU and CEE - http://www.pharmaregist.com Offers drug and medical devices registration and maintenance in EU.

Pharmaceutical Regulatory Services, Inc. - http://www.pharmregservices.com Provide clinical and regulatory support of all phases of global drug development with operations in over 80 countries on all continents.

PharmaCon GmbH - http://www.pharma-con.ch/ Consulting in regulatory strategy for medicinal products.

Pharmacovigilance - http://www.pharmacovigilanceunit.com Consultancy based in Italy that offers scientific services and regulatory affairs for the pharmaceutical industry.

Pharmalink Consulting - http://www.pharmalinkconsulting.co.uk For all European regulatory affairs issues - CTA/IMPD submissions, regulatory compliance issues, and CMC

PharmaReady - http://www.pharmaready.com/ PharmaReady™ is a fully integrated web-based eDMS and eCTD Submissions Solution Suite.

PharmAssure - http://www.pharmassure.com.au Australian pharmaceutical consulting services for validation and FDA and TGA GMP/GLP compliance.

Phoenix Regulatory Associates, Ltd - http://www.phoenixrising.com Regulatory affairs consultants based in the Washington DC metro area with the industry and FDA expertise to aid small to large pharmaceutical and medical device companies.

PinneyAssociates - http://www.pinneyassociates.com/ 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.

PRISYM ID Compliant Barcode & Labeling - http://www.prisymidinc.com 21 CFR Part 11 validated barcode and labeling solutions for pharmaceutical and medical device manufacturers.

PrisymID Life Sciences - http://www.prisymls.com Validated labeling systems and inventory management software systems designed specifically for FDA 21 CFR Part 11 regulated environments.

ProSource - http://www.prosourcedev.com/ ProSource has developed a portfolio of software solutions.

PRS Clinical Ltd - http://www.prs-clinical.com Provider of clinical trial services

PSF Medical - http://www.psfmedical.com European business support and authorised representative for small medical device companies.

Q-NET LLC - http://www.ce-authorizedrepresentative.eu 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.

QMR, LLC - http://www.qmr-llc.com Medical device, pharmaceutical, diagnostic, and other life science quality assurance and regulatory affairs consulting services.

QRC Associates - http://www.qrcassociates.com QRC Associates provides management with cGMP and QSR advice.

Qserve Group - http://www.qservegroup.com/ Qserve® Group B.V 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.

QualiMedd - http://www.qualimedd.com An independent UK management consultancy working within the areas of product development specializing in medical devices and in-vitro diagnostics.

Quality First International Ltd. - http://www.qualityfirstint.com 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

Quality Implementation Services Inc. - http://www.qisfdaconsultants.com Provides consulting services to pharmaceutical, medical device, and life sciences industries in quality assurance, quality control, and regulatory affairs compliance.

Quality Medical Regulations Services - http://www.qmrs.com/ Provides quality assurance documentation support. Assists in site licensing, product registration, HACCP development and implementation. Ottawa, Canada.

Quality Solutions - http://www.validationprofessionals.com Validation Professionals, Inc. (VPI) offers a full range of validation, compliance and technical services for the pharmaceutical, biotechnology and medical device industries.

Quality Systems Laboratories - http://www.qslabs.com Provides compliance process management and eLearning products and services.

Quality Vectors - http://www.quality-vectors.com Provide validations, cGxP compliance, systems engineering, and quality systems to pharmaceutical, medical device, and biotechnology industries.

Qware Riskmanager - http://www.risk-online.com 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.

R. A. Q .A. Associates - http://www.raqaassociates.com 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.

Reg-info.com - http://www.reg-info.com/ A collection of links to websites with information relating to regulatory affairs for pharmaceutical professionals.

Reg123.com - http://www.reg123.com Reg123.com is a portal for the new medicinal product development community with a focus on regulatory affairs and the pharmaceutical drug development process.

RegIntel Ltd. - http://www.regintel.com Provides international regulatory solutions to the pharmaceutical and biologics industries.

Regulatory Affairs Associates LLC - http://www.regaffairs.net RAA (regulatory affairs consultancy)

Regulatory Affairs Consulting - http://www.newdrugapprovals.com Regulatory affairs consulting services to the pharmaceutical and related industries.

Regulatory Affairs Syndicator - http://regulatory.schwoebel.net This website syndicates material for regulatory affairs professionals. Feeds are obtained from a variety of global resources about the US Food and Drug Administration.

Regulatory Affairs, North America LLC - http://www.ranallc.com Regulatory affairs consultancy headquartered in North Carolina.

Regulatory Bureau "Cratia" - http://www.bureaucracy.com.ua Consulting and active assistance in registration (regulatory affairs) and clinical trials of medicinal products, API's, supplements, and medical devices in CIS countries (Ukraine, Russian Federation, Kazakhstan, Moldova, Byelorussia).

Regulatory Pharma - http://www.regulatorypharma.com/ Regulatory Pharma provides regulatory affairs consultancy services (registration and reimbursement of medicinal products (Rx, OTC, plant origin), medical devices, food supplements, and cosmetics) in Poland and Romania.

Regulatory Services Co., Inc. - http://www.raqaconsulting.com Regulatory affairs and quality assurance consulting for entrepreneurial medical device companies.

RegulatoryPro.com - http://www.regulatorypro.com RegulatoryPro offers regulatory affairs consulting services to the biopharmaceutical, medical device and other FDA-regulated industries.

Samarind Regulatory Management Software - http://www.samarindrms.co.uk Samarind RMS is a software package for the pharmaceutical industry that manages regulatory affairs and licence submissions.

SeerPharma - http://www.seerpharma.com.au SeerPharma is a professional consultancy specializing in the delivery of technical compliance and validation, QA knowledge, and GMP training solutions to the pharmaceutical, medical device and biotechnology industries.

Seraphim Life Sciences Consulting LLC - http://www.seraphimlifesciences.com/ Seraphim provides integrated consulting and due diligence on regulatory and operations issues for life sciences companies and investors.

Shafi Consultancy - http://www.shaficonsultancy.com/ Firm specializing in providing SAS training and expertise in working with clinical trials.

Shay Ginsbourg - http://www.ginsbourg.com Israeli consultant experienced in various regulatory certifications, as well as, verification and validation of software and medical devices.

Sigma Biomedical - http://www.sigmabiomedical.com Sigma Biomedical supports biomedical research and medical device development by providing custom solutions.

SimPILy Read - http://www.simpilyread.co.uk/ Offers patient information leaflet readability tests, compliance reviews and advice on leaflet improvement for international pharmaceutical and traditional herbal medicines industries.

SMB Validation and Compliance Services Group - http://www.smbvalidation.com/ SMB Group is designed to get your equipment into production promptly while ensuring that all regulatory requirements are systematically fulfilled with a minimum of interference with operations.

Smith and Associates - http://www.fdaconsultants.com/ A consulting firm specializing in regulatory affairs for medical device manufacturing.

Spherelink FDA Consulting - http://spherelink.com Spherelink provides FDA consulting and international trade consulting between Asia and the United States.

Strategic Compliance International, Inc. - http://www.sci-nc.com SCI, Inc. specializes in regulatory compliance consulting for biologics, medical devices and drug companies.

Supremus Group - http://www.training-hipaa.net/ Provides HIPAA training courses in multiple formats both onsite and online.

Tarius A/S - http://www.tarius.com/ Provides the pharmaceutical, biologics and medical device industries with regulatory and compliance information. Includes services provided, company news and events.

TDC Software - http://www.tdc.fr/en/products/tdc_fmea.php TDC Software is an engineering software suite covering risk management.

Tecno-med Ingenieros - http://www.tecno-med.es/ Located in Barcelona, Spain - helps manufacturers to obtain CE mark for their medical devices.

The Arazy Group - http://www.arazygroup.com Medical Device RA and Quality System Consultants

The Gnomon Group, LLC - http://thegnomongroup.com Regulatory affairs consulting services based in Research Triangle Park NC covering the pharmaceutical and biotech industries, including regulatory strategy, FDA submissions, safety review, foreign company filings, and marketing review.

The Horizon Phoenix Group LLC - http://www.horizonphoenix.biz Quality/regulatory consultants for medical device, pharmaceutical and biotechnology industries. Services include: CE Marking, Authorized European Representative, USFDA, 510ks, PMAs, US Agent and Canadian Licenses.

The Matthews Consultancy - http://www.tmconsultancy.com/ European pharmaceutical/biotech consultancy specializing in project management, medical writing, and business development.

The Tamarack Group - http://www.thetamarackgroup.net Tamarack Group consultants (Charmaine Sutton, Carol DeSain) provide regulatory approvals and compliance services (GMP, QSR) for product development and manufacturers of medical products (US FDA, EU, Canada).

Thermal Compliance Ltd - http://www.thermalcompliance.co.uk Thermal mapping and autoclave validation

THINQ Compliance Ltd. - http://www.thinqcompliance.com/ The integration of services and software to provide competitive compliance, quality advocacy and thought leadership.

Thomas E. Colonna Ph.D./J.D. & Associates - http://www.tcolonna.com 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.

TopPharm Consulting - http://www.regulatory-affairs.pl/ Regulatory affairs consultancy in Poland and EU (MRP, DCP, national, medical devices, food supplements, and scientific dossier consultation).

Torrington Gower Consultants - http://www.torringtongowerconsultants.com Regulatory affairs consultants specializing in CMC/ Clinical National (UK and IE) submissions (renewals and variations).

TRAC Services - http://www.tracservices.co.uk/ A UK based company providing regulatory affairs consultancy and patient information leaflet user testing to the pharmaceutical industry.

Tumont Limited - http://www.tumont.co.uk Specializes in providing cGxP equipment and software validation support to pharmaceutical laboratories in UK. They can provide plans, protocols, reports, SOPs, inventories and training on a fixed cost basis.

UK Medical Device Consultancy - http://www.medicaldeviceconsultancy.co.uk Provides medical device companies with business development services from regulatory affairs, quality systems to strategic reviews, marketing advice, strategic market research, product management from concept to market, business planning, distribution and partner search.

Universal Regulatory Inc. - http://www.universalregulatory.com Specializing in regulatory strategy development, preparation, and review of regulatory submissions.

Validation and cGMP Compliance - http://www.cqionline.com/ Equipment and Software Validation. Part 11 of 21 CFR Compliance. Regulations, cGMP, Validation knowledge base. FDA Warning letters.

Validation in Partnership Ltd - http://www.vipltd.co.uk Specializing in the provision of validation and CGMP (Current Good Manufacturing Practice) compliance services.

Validation Online Net - http://www.validation-online.net Generic downloadable documents that are cGMP compliant.

Validation Systems, Inc. - http://www.validationsystems.com We 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.

Validation Technologies, Inc. - http://www.validation.org/ Worldwide validation, quality, compliance, and production services for the medical device, pharmaceutical, nutraceutical, and biotechnology industries.

Veirup Consult - http://www.veirupconsult.dk Danish regulatory affairs consultancy

VTS Consultants, Inc. - http://www.vtsconsultants.com Validation and regulatory consulting services for the pharmaceutical, biotechnology, and medical device industries.

Wainwright Associates - http://wainwrightassociates.co.uk UK based regulatory affairs consultants offering a wide range of services to international companies in the pharmaceutical, medical device, nutritional and healthcare industry.

Waters Corporation - http://www.21cfrpart11.com A resource for issues surrounding the FDA's 21 CFR Part 11 Rule on electronic records and signatures.

WellKang LLC - http://www.510k.us/510k-submission-procedure.html Regulatory affairs consultancy specializing in medical devices.

Wolter Kluwers MediRegs - http://www.mediregs.com Compliance and risk management software solutions for your business. Specializing in healthcare billing compliance, ERM (enterprise risk management), food, drug and medical device compliance, and grant management compliance.

www.delcornosas.com/ - http://www.delcornosas.com/ Services to the pharmaceutical industry, aimed at obtaining the appropriate authorizations in Italy and Europe.

xfda consulting - http://www.xfda.com xFDA consulting provides services to small and mid-sized pharmaceutical and device companies including biotechnology in the areas of preclinical, clinical, CMC and regulatory.

Zeta Consulting - http://zeta.jo Informatics oriented organization involved in multiple validation and implementation projects in the pharmaceutical and clinical trials industries.

Zodiac Pharmaceutical Services - http://www.zodiacpharma.com/ Provides consulting services in the areas of patent, regulatory affairs, marketing research, and QA/GMP documentation for small to medium size pharmaceutical companies.

Help build the largest human-edited directory on the web. Submit a Site - Open Directory Project - Become an Editor

The content of the Google directory is based on the Open Directory and is enhanced using Google's own technology. The following Open Directory editors contributed to this category: dctec

Modified by Google - ©2009 Google
Advertise with Us - Jobs, Press, Cool Stuff...