Top 100 alternative sites to accelagen.com.au
AD Modum R&D | Research and development of medical devices
AD Modum R&D: research and development of medical devices with the max respect of the quality regulatory. Only the best services to healthcare companies.
Pharmaceutical Recruiting | Pharma and Biotech Recruiter | TriNet Pharma
Pharmaceutical, Biotech, Medical Device, and Diagnostics recruiting. Medical Affairs. Regulatory Affairs. Clinical Operations. Med Comms.
Pharmaceutical and Regulatory consulting | Medical Devices
PDS is a pharmaceutical and regulatory consultancy serving the pharmaceutical, biopharmaceutical, medical device and cosmetic industries.
Author: Anicca Solutions A W-Fowler
Medical device design
Pharmaceutical and medical device design and development.
Expert Medical Device Consulting | US and EU | Kapstone Medical - Kapstone Medical
Kapstone Medical integrates with medical device companies at every stage of the product life cycle. Quality Assurance, Regulatory Affairs, Product Development and Manufacturing Solutions.
Medical Device Consulting | QA/RA Consulting Group
QA/RA Consulting Group - FDA Quality & Regulatory Affairs for Medical Devices. Specializes in bringing new medical devices to market offering services including domestic and international regulatory affairs, design and development, quality management systems, auditing, and usability engineering.
CRO for ****, Biologic, & Medical Device Programs | Medpace
Medpace is a clinical research organization (CRO) conducting global clinical research for the development of drugs and medical devices. Read on.
Medical Devices Consulting
MDC Engineers and Manager Regulatory Affairs provide medical-technical and regulatory knowledge. We consult, design and manufacture medical devices, in-vitro-diagnostic and laboratory equipment, which reflect the state-of-the-art and fulfill market-specific regulatory requirements.
Author: GWK Präzisionstechnik GmbH
Medical Devices Consulting
MDC Engineers and Manager Regulatory Affairs provide medical-technical and regulatory knowledge. We consult, design and manufacture medical devices, in-vitro-diagnostic and laboratory equipment, which reflect the state-of-the-art and fulfill market-specific regulatory requirements.
Author: GWK Präzisionstechnik GmbH
CMC MEDICAL DEVICES - YOUR QUALITYIS OUR SERVICE
EC REP of Medical Devices, Consultant of CE mark, ISO 13485, OBL Agreements, Regulatory Affairs
Compass for Medical Device Development | Synergio
Compass guides medical device development teams through their product development and regulatory processes and make the creation of submission deliverables a fluid part of daily tasks.
Medical Device Consult - Medical Device Consult
Medical Device Consult is specialised in Medical Device and In-Vitro Diagnostic companies in meeting US & European regulatory...
Clinical Trial Experts
We support pharmaceutic companies from the following sectors: clinical monitoring, medical monitoring, clinical **** research, pharmaceutical **** safety and Regulatory Affairs for drugs and medical products.
FDA Consultants | Medical device consultants | pharmaceutical consultants |
FDA consulting for the medical device industry, pharmaceutical industry and food industry for US and EU FDA quality assurance and regulatory compliance and medical Device Reimbursement %
Medical device regulatory, clinical, and technical services
Paladin Medical®, Inc. offers a full range of medical device regulatory, clinical, and technical services for premarket applications and regulatory compliance.
Prodct, LLC | Boston MA | Medical Device Development | Advisory
Prodct supports innovative biotech, medical device, and therapeutic companies through the creation and execution of holistic, efficient, and practical product development + manufacturing strategies to accelerate paths to clinical, regulatory approval, and market
Proskauer in Life Sciences - Developments and trends in therapeutics, pharmaceutical, biotechnology and medical devices
Developments and trends in therapeutics, pharmaceutical, biotechnology and medical devices.
Author: Stephanie A Diehl; Baldassare Vinti
Devintec - Advanced R&D in substance-based medical devices
Devintec is a privately owned pharmaceutical company based in Switzerland pioneer in research and developing innovative substance-based medical devices.
Medical Device Regulatory Consultants & More | Cofactortech.com
Cofactor Technologies provides international quality assurance and regulatory affairs consulting services to medical device companies worldwide.
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Medical Device & Pharmaceutical Consulting and Staffing Agency | Network Partners
Learn more about Network Partners, a medical device and pharmaceutical consulting and contract staffing agency providing packaging engineering, regulatory affairs, labeling, cold chain solutions and project management.
Medical Device Quality Management System | LuminLogic Software
Lumin Logic is a premiere Medical Device Quality Management System used for medical device research, testing and regulatory compliance.
Devicia - Your Medical Device CRO
Devicia is a clinical research organization (CRO) focused exclusively on Medical Devices. And as Medical Device CRO we guide and support you.
Mexican Health Registry for Medical Devices
Regulatory affairs and technical consultancy services specialized in Mexican sanitary regulation of medical devices for obtaining health registry from COFEPRIS
Medical Devices QMS and Regulatory Affairs Melbourne
We specialise in Quality Assurance and Regulatory Affairs for Medical Device companies, achieving 100% compliance for all our clients
Homepage - RFT Group
The RFT Group recruit exclusively for science and engineering jobs in pharmaceutical, Medical Device, Quality Assurance, Regulatory Affairs, Supply Chain, **** Development, Clinical Research, HR, **** Manufacturing, Sales & Marketing and Finance sectors.
EROND - Medical Devices | Medical Furniture | R&D
Medical devices and customized medical furniture producer, made in Romania. Research and development projects in medical field.
BPS - Home
Pharmaceutical Recruitment; Pharmaceutical Training; Pharmaceutical Consulting; Biotech; Biotechology; Healthcare; Clinical research; CRA; Regulatory Affairs; Regulatory Consulting; Consultants
Author: Bio Pharmaceutical Solutions; Get Started Pty Ltd
Thinki – pharmacovigilance Clinical Trials and medical writing services partner
Think-i offers analytics, Forecasting, pharmacovigilance, clinical trials, regulatory & medical writing solutions to the pharmaceutical companies and medical devices companies.
Aix Scientifics ® - Clinical Research
an European Contract Research Organisation (CRO) planning, implementing and evaluating clinical research for pharmaceutical products and medical devices.
Aix Scientifics ® - Clinical Research
an European Contract Research Organisation (CRO) planning, implementing and evaluating clinical research for pharmaceutical products and medical devices.
Aix Scientifics ® - Clinical Research
an European Contract Research Organisation (CRO) planning, implementing and evaluating clinical research for pharmaceutical products and medical devices.
Aix Scientifics ® - Clinical Research
an European Contract Research Organisation (CRO) planning, implementing and evaluating clinical research for pharmaceutical products and medical devices.
Medical device distributor | Cytostatics | codan usa
Codanusa is Our success is based on 50 plus years of medical research, pharmaceutical development, and clinical experience, which has resulted in a level of quality and service that is unsurpassed.
Only Medics: Recruiting Pharmaceutical Physicians
Only Medics is a specialist recruitment agency for Pharmaceutical Physicians, hiring for biotechnology, Clinical Research(CRO), Regulatory Authorities.
BioVera - Medical Device Testing, Development, Research and Marketing in the United States and Canada.
BioVera, LLC and BioVera, Inc. provide medical device and biomaterial testing, research, development, and marketing services, including process evaluation, and regulatory requirements in both the United States and Canada.
Ivowen | Regulatory Affairs Specialists
Regulatory affairs consultancy specialising in human and veterinary pharmaceuticals, pharmacovigilance and medical devices
raPHARM regulatory affairs consulting and education
raPHARM is a consultancy and education office specialising in pharmaceutical and medical devices regulatory affairs.
Hylomorph | Switzerland | Implantable Medical Devices
Hylomorph is a clinical-stage medical device company developing innovative materials designed to transform the biocompatibility of implantable medical devices.
Medical Device Developments
Medical Device Developments is a procurement and reference site providing a one-stop-shop for professionals and decision makers within the global Medical industry
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Independent Solutions | Pharmaceutical, BioPharmaceutical and Medical Device Consultancy/Talent Placement
Independent Solutions delivers impartial advice and practical hands on solutions to the Pharmaceutical, Biotechnology and Medical Devices industries.
CaRACS - Clinical and Regulatory Affairs Consulting Services
CaRACS - Clinical and Regulatory Affairs Consulting Services, is dedicated to Clinical Development Strategy and Regulatory Affairs Consulting Services for biotechnology and pharmaceutical industries.
Author: Michael Beckert
CaRACS - Clinical and Regulatory Affairs Consulting Services
CaRACS - Clinical and Regulatory Affairs Consulting Services, is dedicated to Clinical Development Strategy and Regulatory Affairs Consulting Services for biotechnology and pharmaceutical industries.
Author: Michael Beckert
CaRACS - Clinical and Regulatory Affairs Consulting Services
CaRACS - Clinical and Regulatory Affairs Consulting Services, is dedicated to Clinical Development Strategy and Regulatory Affairs Consulting Services for biotechnology and pharmaceutical industries.
Author: Michael Beckert
CaRACS
CaRACS - Clinical and Regulatory Affairs Consulting Services, is dedicated to Clinical Development Strategy and Regulatory Affairs Consulting Services for biotechnology and pharmaceutical industries.
Author: Michael Beckert
CaRACS - Clinical and Regulatory Affairs Consulting Services
CaRACS - Clinical and Regulatory Affairs Consulting Services, is dedicated to Clinical Development Strategy and Regulatory Affairs Consulting Services for biotechnology and pharmaceutical industries.
Author: Michael Beckert
CaRACS - Clinical and Regulatory Affairs Consulting Services
CaRACS - Clinical and Regulatory Affairs Consulting Services, is dedicated to Clinical Development Strategy and Regulatory Affairs Consulting Services for biotechnology and pharmaceutical industries.
Author: Michael Beckert
Rømer Consulting – Regulatory Navigation for Medical Devices
Regulatory Navigation for Medical Devices
ARQon Singapore - Medical Device Consulting, Regulatory, Medtech
ARQon is a medical device consultant for Regulatory, Quality RA/QA, device registration, clinical trials, ISO13485, GDPMD, MDSAP and distribution consulting.
Baat Medical | Medical Engineering
Medical device engineering for spine & joint implants ✅ Clinical validation ✅ Regulatory approval, ✅ Clinical evaluation & marketing for medical devices.
Author: Admin
CRO Services | Avion Medical | Hawthorn
Avion Medical is your specialist health solutions partner from Research to Commercialisation – we provide consulting, medical affairs and clinical research services for pharma, biotech and medical devices
Pharmaceutical Jobs and Recruitment : Clinical Professionals
Pharmaceutical jobs from Clinical Professionals, specialising in the clinical recruitment industry for clinical research jobs, regulatory affairs and biostats.
Regulatory Affairs, Quality Affairs, Pharma Consultancy by Baggerman
Supports companies in Pharmaceutical, Medical Device and Cosmetics Industry. Regulatory Affairs, Quality Affairs, Pharmacovigilance Promotional Control
Medical Devices | Eye-D | Copenhagen
Engineering & Design Consultancy for medical devices. Product development research, analysis, prototyping and implementation.
Home - Medical Device Regulation and ISO quality standard
Want to Master Medical Device Regulation & learn how to put a product on the market in Europe. Easy Medical Device is a platform for tools and resources for Regulatory Affairs, Quality Management, Regualtory Compliance. Learn how to choose your notified body or how the device regulation is different in other countries
Author: Monir El Azzouzi
Orthogonal - Medical Device Software Design & Development
Orthogonal is a software developer for connected mobile medical devices (CMMD) and software as a Medical Device (SaMD).
Regulatory Affairs Consultants Ireland, Pharmaceutical Regulatory Compliance Service
EMRC, Regulatory Affairs, Pharmaceutical, Consultancy, Advice, Medical Device, Registration, CE Marking , Wholesale Services
Welcome to Smerud Medical Research - Smerud Medical Research
Smerud Medical Research is a European contract research organisation (CRO). We conduct clinical trials to advance new medical compounds, helping pharmaceutical and biotechnology companies with clinical project management, proof of concept and phase ii.
Medical Device News Magazine
Medical Device News Magazine reports breaking medical device industry news, medical device executives on the move, clinical trials and more.
Author: Medical Device News Magazine; A Division Of Ptm Healthcare Marketing; Inc
Medical Device CRO | Archer Research
Your personal partner to future proof your clinical evidence. Archer Research is a full-service CRO specialized in Medical Devices.
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Medical Device Development | Point of Care Testing Devices
Ximedica is one the best amongst medical device development companies. It has over 30 years of experience in point of care testing devices. Explore our products
MarcM Consulting Canada - Regulatory Affairs Consultants - Welcome
Regulatory affairs consultants serving pharmaceutical and related industries in the Americas and globally. Specializing in regulatory compliance and business development for pharmaceuticals, medical devices, veterinary medicines, cosmetics, natural health products and related OTC wares.
Author: MarcM Consulting Canada
Pharma Search Partners, Inc. is a pharmaceutical industry placement service specializing in the placement of highly skilled professionals in
Pharma Search Partners, Inc. is a pharmaceutical industry placement service specializing in the placement of highly skilled professionals in permanent or temporary positions in such fields as Pharmacoeconomics, Pharmacoepidemiology, Medical Directors Regulatory, Compliance and Manufacturing. We have set up teams in the UK, India, and Singapore, to name a few. Our recruiters have pharmaceutical industry experience ranging from pre-clinical research, clinical research, sales & Marketing, regulatory affairs, quality assurance, and information technology, research and development and Medical Affairs.
Training for Pharmaceutical and Medical Device | NXLevel Solutions
Pharmaceutical and medical device compliance training.
United Kingdom - PharmaLex
For companies in the global pharmaceutical, medical devices and healthcare industries that require expert advice and practical, hands-on support in regulatory affairs, pharmacovigilance and development consulting.
Author: PharmaLex @PharmaLexGLOBAL
Medical Device Registration System - Regulatory Consulting|LICENSALE®
LICENSALE® is a global medical device registration system that lets you take full control of your regulatory affairs and gain approvals in 140 countries.
ADM Tronics, Inc. | Electronic Medical Device Design & Development
ADM Tronics (“ADMT”) is a full service electronic medical device innovation firm. Our multi-disciplinary in-house team of researchers, designers, engineers, regulatory and manufacturing experts bring diagnostic and therapeutic medical technologies from concept through production.
Medidee Services - RA, CA/CRO and QA, for MedTech
Medidee: consulting in regulatory affairs, quality insurance, clinical affairs and digital health for medical devices and in vitro diagnostics.
Whitney Consulting Ltd - China Medical Regulatory and Clinical Affairs
Explore Whitney Consulting's Free Resources Resource Materials Whitney Consulting is a regulatory consulting firm dedicated to the Chinese market. Since 1994, we have been providing international clients with services in Chinese medical device regulatory affairs, clinical affairs, and medical market research. From our offices in the United States and China, we bring clients up-to-date
Author: Whitneyconsulting
International Medical Device Regulators Forum
The purpose of the IMDRF is to accelerate international medical device regulatory harmonization and convergence
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