Celebrating 10 Years of Business Consulting Services
SGR Consulting Services are a consultancy and outsourcing service established in 2005 offering a unique service to companies that would like to implement UKAS certified Management Systems. We work with businesses to implement Quality, Medical, Environmental, Health & Safety, Information Security management systems and integrate the processes into day-to-day business practice.
SGR Consulting Services provide a bespoke system, building on the clients existing system and introducing new and improving existing procedures only where required. This method of
implementation reduces the need to retrain existing staff and encourages ownership of the system among the staff. We provide a professional collaborative external resource to implement and
manage our clients’ systems that are built around a robust and easy to implement framework. The introduction of a documented management system provides a sound framework for all members of the company to work to. When correctly designed and implemented, it will act as a catalyst for improving your organisation’s performance, allowing you more time to run your business.
For designers, manufacturers and/or distributors of medical devices, we also provide regulatory affairs advice and assist in CE Marking and worldwide device approvals. This ensures that your legal responsibilities are met under the European Medical Device Directive (MDD), US FDA 21.CFR 820, Health Canada and other worldwide regulatory requirements.
We work with both SME and large worldwide organisations, providing advice and training services across a range of business activities.
We are platinum members of the BSI associate consultants programme (membership No. 24) this provides us with access to benefits that we can pass onto our clients such as 20% discount on BSI public and in house training courses.
Consultancy Team and Key Competences
Master of Business Administration (MBA), Lead Auditor ISO 9001:2015 and ISO 13485:2012, IOSH National Diploma in Occupational Health and Safety.
20 Years’ experience in the medical device industry in both middle and senior management positions, 10 years’ experience as a consultant in ISO 13485, ISO 9001, ISO 14001, OHSAS 18001 and ISO 22000.
Biomedical Engineering (M.Eng), Lead auditor ISO 9001:2015 and ISO 13485, IOSH National Certificate in Occupational Health and Safety.
Consulting experience in the development and implementation of ISO 9001 and ISO 13485, creation of technical files for CE marking, applications for FDA 510(k) clearance.
BSc Honours in Chemistry, Lead auditor ISO 9001:2015 and IOSH National Certificate in Occupational Health and Safety.
35 Years’ experience in Quality and environmental control and management in Pharmaceutical, chemical, paper and print manufacturing industries.
Experienced in ISO 9001, ISO 14001, ISO 27001 and OHSAS 18001.