Quality and Excellence

Similar documents
Accel-Heal. An effective treatment for healing leg ulcers. Guide for Clinicians

Lakshy Management Consultant Pvt. Ltd.

Quality Management System Certification. Understanding Quality Management System (QMS) certification

UALITY SYSTEMS STANDARDS

COMPETENT AUTHORITY (UK) MEDICAL DEVICES DIRECTIVES GUIDANCE NOTES FOR MANUFACTURERS OF DENTAL APPLIANCES

SLEEP IMPROVING WRISTBAND. Item No Owner s Guide

Welcome to presentation By Sanjay Punjabi Lead Auditor for ISO 9001, ISO 14001, OHSAS & BS 7799

About BNM.

ISO 13485:2016 MEDICAL DEVICES QMS TRANSITION GUIDE

NANDTB-F012 Rev 0 Audit Checklist

Market surveillance of medical devices

AGREEMENT ON COMMON PRINCIPLES AND RULES OF CIRCULATION OF MEDICINAL PRODUCTS WITHIN THE EURASIAN ECONOMIC UNION. (Moscow, 23 December 2014)

Contour Your Body Quickly and Comfortably!

The dramatic effect of the one risk you can t see

Medical Devices Act 1

The cost of chronic wounds in the UK has

OHSAS 18001:2007 OCCUPATIONAL HEALTH & SAFETY MANAGEMENT SYSTEM WHITE PAPER Lakshy Management Consultant Pvt Ltd aiming excellence

IAF Mandatory Document. Requirements for the Migration to ISO 45001:2018 from OHSAS 18001:2007 (IAF MD 21:2018)

AQ Group UN Global Compact Communication on Progress AQ Group AB

Accredited Certification International Limited. Migration Q&A

ENVIRONMENTAL, HEALTH AND SAFETY LEGISLATION IN EUROPE

POINT OF CARE DIAGNOSTICS

EHR Developer Code of Conduct Frequently Asked Questions

QA Regulatory forum: Classification and Risk assessment according to MDR Date : T h e r e s e. A l b i n s s o m e d q t e c h.

BEDFORDSHIRE AND LUTON JOINT PRESCRIBING COMMITTEE (JPC)

OHSAS Project Group. Implementation Guidance for migrating from OHSAS 18001:2007 to ISO 45001:2018 CONTENTS 1.0 INTRODUCTION

IT S A FACT TECHNOLOGY EVOLVES. WE MAKE SURE YOU CAN TOO.

ADVANCIA : A TRUE PLATFORM & INNOVATIVE SYSTEM OFFERING EFFICIENT NASAL DOSE DELIVERY

Using Health Economics to Inform the Development of Medical Devices. Matthew Allsop MATCH / BITECIC

Quality, Safety and Sourcing in Unlicensed Medicines

Your Partner in Healing

Syllabus. The University of Florida College of Pharmacy's Pharmacist Immunization Program contains the following modules:

SHERMOND GLOVE RANGE Your first choice for unbeatable quality and medical protection

About BNM.

Pb-Free/RoHS Solutions

This document is meant purely as a documentation tool and the institutions do not assume any liability for its contents

Quality Assurance Policy. for the. Procurement of HIV Point-of-Care Technology. under the UNITAID Grant

FRAMEWORK OVERVIEW. Page 1 of 7

Hammarplast Medical. Disposables

DIRECTIVES. (Text with EEA relevance)

Cost and dressing evaluation of hydrofiber and alginate dressings in the management of community-based patients with chronic leg ulceration

Maximizing Sustainability Through Reprocessing Single Use Devices

15. Procuring, processing and transporting gametes and

User Manual.

Preparing a US FDA Medical Device 510(K) Submission

Establishing LCA in the Healthcare Sector

COMMISSION OF THE EUROPEAN COMMUNITIES

GAVI, THE VACCINE ALLIANCE

EUR-Lex L EN. Council Directive 93/74/EEC of 13 September 1993 on feedingstuffs intended for particular nutritional purposes

User Manual Table of Contents. Instructions for Using the LaserTouchOne Charging the Unit... 5 Holding the Device... 5 Treatment Steps...

Costing report: Lipid modification Implementing the NICE guideline on lipid modification (CG181)

Drug and Alcohol Testing

Shareholder Presentation Annual Meeting 2018

11/5/2009. Dignity Challenges Dignity in Care Campaign, Devices for Dignity HTC: Mission. D4D Role in Assistive Technology. Assistive Technology

XOSERVE LIMITED SERVICES SCHEDULE FOR THE PROVISION OF NON-CODE USER PAYS SERVICES (REFERENCE NUMBER XNCUP(SS)06) DATED 20 INTRODUCTION

Professional Wound Management

BEST PRACTICE CHANGE CONTROL : DECIDING WHEN TO SUBMIT A 510(K) FOR A DEVICE CHANGE. Yuan Xu 18- JAN- 2018

Reader and Sensor Demo Kit. Quick Start Guide

OECD WORKSHOP: THE ENVIRONMENTALLY SOUND MANAGEMENT OF RECOVERABLE WASTES (ESM) SESSION 1

Alpha-Bio Tec specializes in the development and production of advanced dental solutions, focusing on the fields of implants and prosthetics. Over the

NEGATIVE PRESSURE WOUND THERAPY

Falsified Medicines Directive (FMD) Dispensing Doctors Association Wednesday 18-Oct-17 Jerome Bertin

ProPocket TM. User Guide

Automated external defibrillators

LEAF Marque Assurance Programme

English. Standard. StandardCylindrical

Professional body composition analysis: BODYSTAT I500. Touch Screen THE SCIENCE BEHIND CLINICAL BODY ASSESSMENT.

1ª Jornada de Análisis de Riesgos en RT. 10 de Dic 2014 José Luis Roldán

STANDARD OPERATING PROCEDURE SOP 720 RISK ASSESSMENT OF TRIALS SPONSORED. BY THE NNUH and UEA

Welch Allyn HScribe Holter Analysis System

Better Diagnostics for Life

Medical - Combined Medical Devices Guideline

Informed Consent Procedures and Writing Informed Consent Forms

International Hearing Society Middlebelt Rd., Ste. 4 Livonia, MI p f

Innovative Range of Regenerative Solutions

Lowering epilepsy-related treatment costs in the era of patient choice and value-based care

End Vinyl Glove Worries. Relax with Lavender *.

IMPLEMENTATION COURSE (MODULE 1) (ISO 45001:2016 AVAILABLE ON REQUEST) COURSE DURATION: 3 DAYS FOR OHSAS 18001:2007 OR ISO 45001:2016

Phonak PilotOne II. User Guide

MEDICAL DEVICES. our advice on. automated external. defibrillators

Policy: S5 Smoke Free Policy

Professional body composition analysis: BODYSTAT I500 THE SCIENCE BEHIND CLINICAL BODY ASSESSMENT.

NO SMOKING POLICY POLICY IMPLEMENTATION CHECKLIST

UPPER MISSOURI DISTRICT HEALTH UNIT REGULATIONS FOR TANNING FACILITIES

User Guide. For Jacoti Hearing Center Version 1.1. Manufacture Year 2016

GLOBAL NEUROSTIMULATION MARKET

VelaShape II. Cellulite Treatment & Body Contouring. Science. Results.Trust.

Compact Massager Instructions

Workshop on the reprocessing of medical devices. 5. December Brussels. Nikou Ghassemieh Managing Director

TruGuard Custom Tongue and Jaw Positioner Instructions for Use

COCHLEAR NUCLEUS RELIABILITY REPORT. Volume 14 February 2016

Global Harmonization Task Force SG3 Comments and Recommendations ISO/DIS 9001: 2000 and ISO/DIS 9000: 2000 And Revision of ISO and 13488

Value creation through profitable growth Danske Bank Winter Seminar 2017, Copenhagen Lars Rasmussen, President & CEO

The Prime Minister s Challenge on Dementia Lorraine Jackson Deputy Director: Dementia Policy Department of Health 12 April 2016

a practical guide ISO 13485:2016 Medical devices Advice from ISO/TC 210

Current through Chapter 199 and Chapters of the 2015 Legislative Session

Traditional Silicone Technology

The Practice Standards for Medical Imaging and Radiation Therapy. Sonography Practice Standards

PartnerIng with Home Energy Scotland

Transcription:

Quality and Excellence

What is Accel-Heal? Accel-Heal is a compact (7cm x 4cm x 2cm), certified and patented, battery powered electroceutical treatment device (Class IIA) designed to improve and accelerate healing rates in patients with complex wounds. What is an electroceutical? Practically all of the body s organs and functions are regulated through neural circuits communicating via electrical impulses, it should therefore be possible to interpret the electrical language of disease from the level of gene expression upwards. By extension, it is then possible to stimulate, inhibit or change a malfunctioning pathway in order to correct the defect. The new term for this innovative area of medicine is electroceutical. Unlike the universal term previously used, e-stim, electroceutical implies a more accurately targeted application more akin to its pharmaceutical equivalent. Synapse Accel-Heal s parent company is leading the way in this area of medicine with the development of a clinically relevant electroceutical with its patented Synapse Sequence found within the compact Class IIA device Accel-Heal. How do I know that Accel-Heal is safe to use? Accel-Heal is designed and manufactured to conform with the highest standards of quality and safety. It adheres to the quality standards dictated by the International Organization for Standardization (ISO), Medical Devices Directive, Medical Device Classification and CE marking.

Why should I use Accel-Heal? Developed and designed with ease of clinical application and patient comfort in mind, Accel-Heal used along standard dressings without a need for a change in the treatment plan, improves treatment outcomes and quality of life for patients with complex wounds. Independent clinical trials demonstrated that Accel-Heal made a significant reduction to wound size, exudate levels and pain in 95% of patients, with 38% achieving full closure. Accel-Heal improves and accelerates healing rates, while significantly contributing to cost savings. 15% reduction ( 6.2 million) in costs to the NHS, over a five moth period, demonstrated via independent health economics analysis (cost per QALY of minus 7,696) and a 27% reduction in nurse visits. ISO explained ISO is an independent organisation that creates standards for all kinds of industries. It is mainly targeted towards the European market although some other countries also adopt ISO standards. What is ISO 9001? ISO 9001 is a general set of quality system standards for companies. If a company complies with the ISO 9001 standard, this means that the company is organised in such a way as to obtain a high level of customer satisfaction, and to continually improve this organisation. Compliance with the standard is certified by an external accreditation body. Synapse Electroceutical Ltd the home of Accel-Heal is ISO 9001 accredited, ensuring highest standards of customer satisfaction and commitment to continued improvement.

What is ISO 13485? ISO 13485 is based on ISO 9001, but with specific adaptations for companies that manufacture medical devices. These adaptations relate to: making sure that patient safety is kept in mind during all phases of the product design making sure that the product complies with regional or national laws concerning medical devices rather than continually improve (see ISO 9001), this standard asks to maintain the level of efficiency within the organisation. Synapse Electroceutical Ltd the home of Accel-Heal is accredited with ISO 13485 ensuring patient safety, compliance with regional and national laws and maintaining standards of efficiency within the organisation. What is MDD 93/42/EEC? The European Union has created the Medical Device Directive (MDD) to regulate the market in the medical device sector. The MDD stipulates all essential requirements that must be met by the device when it is put on the European market. The conformity of the product with the MDD requirements is assessed by an external accreditation body. Accel-Heal meets and complies with all essential requirement stipulated by the MDD.

What does a CE-mark mean? A CE (Conformité Européenne) mark indicates that a product complies with the European Directive that applies to it. Medical devices, in order to be granted a CE mark must meet all essential requirements of the MDD. Accel-Heal is marked with a CE mark as it meets and complies with the MDD essential requirements and carries CE 0120 reference number. Medical Device Classification and the meaning of a Class IIA classification If a product is a medical device it should be given a classification based on the risk it poses to the patient or end user. Accel-Heal is a Class IIA device as it is an active therapeutic device intended to administer or exchange energy to/from the human body in a non hazardous way. Science behind Accel-Heal Neural circuits communicating via electrical impulses regulate many physiological functions, therefore it is possible to interpret the electrical language of health and disease from the level of gene expression upwards. It is now possible to inhibit or change a malfunctioning electrical pathway in order to correct a potential defect. Accel-Heal is a non invasive, compact Class IIA medical device which uses the patented Synapse Sequence programmed to deliver a specific series of electric energy interactions through the skin to manipulate gene expression to modify specific physiological functions in dermal tissue. www.accelheal.com

Find out more To find out more about Accel-Heal visit www.accelheal.com To find out more about Synapse The home of Accel-Heal visit www.synapseelectroceutical.com Purchase Accel-Heal Please contact us at info@accelheal.com or call us on 01959 569 433 NHS Supply Chain Accel-Heal is available via NHS Supply Chain and SBS Services, Product Code: K560-6 Arrange an educational visit To arrange a non promotional visit to find out more about Accel-Heal, email us on info@accelheal.com or call us on 01959 569 433 Synapse Electroceutical Ltd 1 Churchill Court, Hortons Way, Westerham, Kent, TN16 1BT t: 01959 569 433 e:info@synapseec.com www.synapseelectroceutical.com Company reg.no: 04626631