Medical Device & QA Consultancy Company Profile
Medical Device & QA Consultancy was formed in 1994, to assist Manufacturers of Medical Devices to accomplish their European and/or FDA Regulatory compliance. Through arrangements with our Associate Partners, both in the USA and Europe, we are able to offer a truly all-encompassing Service to the Medical Device Manufacturing Industry
Location
Hannibal House Elephant and castle
London
London
se16TQ
United Kingdom
Contact
Phone: 44 161 980 4310
Fax: 44 161903 9787
Email: info@mdqa.co.uk
News Articles
PAREXEL appoints Larson as VP of evidence development
PAREXEL Consulting, a business unit of PAREXEL International and a global consultancy serving the biopharmaceutical and medical device industries, has appointed Leanne R. Larson as vice president of e...
FDA creates collaborative partnership with medical device makers
The FDA and medical device makers formed a nonprofit organization, the Medical Device Innovation Consortium, to work with one -More- AssurX helps medical device companies meet tough FDA/regu...
Healthcare markets in Asia: updates on the Chinese medical device industry
Ames Gross provides an update on the Chinese medical device industry. The economic success in China has led to higher demand for medical device products and increased opportunities for foreign device...
Zoll gets FDA OK for fully automatic external defibrillator
The FDA has given Zoll Medical, an Asahi Kasei unit, 510(k) clearance to market its AED Plus system. -More- Exporting to Europe: Medical Device Requirements Join BSI to gain a basic underst...
Medical Device Innovation Consortium Launches, Aims To Start Projects In 2013
The first public-private partnership to focus on promoting medical device regulatory science, known as the Medical Device Innovation Consortium, aims to speed up patient access to medical device techn...
Cardiva gains FDA approval for vascular closure device
Cardiva Medical has received premarket approval from the FDA for Vascade, an extravascular closure system used during percuta -More- Exporting to Europe: Medical Device Requirements Join BSI...
UK pharma consultancy signs AllTrials register
UK pharma consultancy signs AllTrials register
Medical Devices Summit Europe, 13-14 November 2012, Dublin
Given the recast of the European Medical Device Directive and the recent changes to the FDA's 510(k), the regulatory climate in the medical device industry is more volatile than ever. Medical Device m...
Drugs and Medications
Pediacare childrens multisymptom cold [Blacksmith Brands, Inc.]
PediaCare Childrens Multi-Symptom Cold
Pediacare longacting cough [Blacksmith Brands, Inc.]
PediaCare Long-Acting Cough
Nitrogen [Blue Water Industrial Products, Inc.]
Gaviscon [GlaxoSmithKline Consumer Healthcare LP]
Drug Facts
PubMed Articles
Global Cardiovascular Device Innovation: Japan-USA Synergies.
Background: Global medical devices have become more popular, but investment money for medical device development is not easily available in the market. Worldwide health-care budget constraints mean...
Abstract Conclusion. Middle ear pressure treatment by the tympanic membrane massage (TMM) device as well as the Meniett device is effective and provides minimally invasive options for intractable vert...
Value Driven Innovation in Medical Device Design: A Process for Balancing Stakeholder Voices.
The innovation process has often been represented as a linear process which funnels customer needs through various business and process filters. This method may be appropriate for some consumer produc...
What information do people needing care and their care-giving relatives need?
BACKGROUND: The recent reform of the German Care Insurance Law (2008) was expanded to include independent consultancy for care issues. The goal of this study was to explore the informational needs of...
A prospective window into medical device-related pressure ulcers in intensive care.
The aim of this study was to determine the prevalence, severity, location, aetiology, treatment and healing of medical device-related pressure ulcers (PUs) in intensive care patients for up to 7 day...
Clinical Trials
Clinical Evaluation of the Interlace Medical Hysteroscopic Morcellator
This study assesses the effectiveness of intrauterine fibroid and polyp removal using the Interlace Medical 1st generation hysteroscopic morcellator device based on a retrospective review...
Evaluating Outcomes in the Placement of Boomerang Percutaneous Device
The purpose of this study is to evaluate the safety and effectiveness of the Boomerang percutaneous closure device following diagnostic cerebral angiography or neurointerventional procedur...
The purpose of this study is to determine if patients in the HeartNet Ventricular Support System with optimal medical and device therapy arm (Treatment group) show statistically significan...
PROSPECT: Predictors of Response to Cardiac Re-Synchronization Therapy
Heart failure is a progressive disease that decreases the pumping action of the heart. This may cause a backup of fluid in the heart and may result in heart beat changes. Using a medical...
The purpose of this experiment is to confirm the results of previous testing of Urodynamix's Uro-NIRS device. Together Urodynamix and Laborie have created a device that includes standard...
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