Profile Summary
I have 3 years of research experience in writing scientific contents i.e research articles, Synopsis, thesis/dissertation etc. I have completed...
Broad hands-on software and hardware development for medical devices such as diagnostic imaging devices (PET, MRI, X-Ray and Ultrasound), blood...
I am the holder of highly prestigious Tier 1 Exceptional Talent Visa and endorsed as such by the Royal Academy of Engineering in the fields of ...
R&D executive with a Masters in Plastics Engineering and 20 years of experience in the medical device industry; worked in both large-ca...
My professional background is to technically write the Scientific content, assess the researcher in research work related to Bioinformatics and...
It's me Dr.Hamdan, professionally computational biologist. My profession, not only professionally, but my passion is to interact with globa...
Fourteen years of R&D, Regulatory and Medical writing experience in various disciplines across In-vitro diagnostics, medical device regulat...
Ph.D. in Chemistry having a total of 14+ years of experience in the pharmaceutical industry, expertise in the regulatory intelligence of pharma...
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PHD pharmacist, with more than 5 years of experience in Quality Assurance (QA) and Regulatory Affairs (RA). My...experience enables me to help you on: -The compliance of your Quality Management System (QMS) (ISO 13485/ISO14971...
I have over 8 years of experience in Clinical Research, Regulatory Affairs and Quality Assurance of implantable and electro medical devices in ...
I am an experienced Quality and Regulatory professional with over 25 years in the medical device manufacturing industry. I have worked with Cla...
Having experience in medical device regulatory affairs, EUMDR, USFDA 510K, ISO 14971, ISO 13485
Juan M. Campos is a Medical Device professional with + 33 years of continued industry experience. His main areas of expertise include Quality A...
Hi, I have 12 years of experience in a multinational Pharmaceutical and Medical Device company as a QA/RA manager. My Specialties -Experience...
Consulting services including application of IEC/EN 60601-1, IEC 62304, IEC 62366, ISO 14971. Project Management - Medical Devices Compliance. ...
A proactive and result-oriented medical device professional with over 25 years of experience in QMS Systems and Regulatory Affairs compliance. ...
I am a process and product development commercialization consultant and project manager with an automation and mechanical engineering backgroun...
A seasoned professional with a decade of experience, I am a Leader and Speaker in the field of Quality Assurance & Regulatory Affairs, ...
I performed inspections and premarket approvals for FDA for 7.5 years. I am now a Senior Consultant operating out of Switzerland. I operate a...
We are a Contract Research Organization (CRO) that focuses on advanced project management, clinical operations, medical writing, statistical an...
Ten + years of hands-on technical working experience in the manufacturing environment covering Metal, Textiles, Food, Auto parts, Chemical proc...
monitoring and advising on the performance of the quality management system, producing data and reporting on performance, measuring against set...
Technology focused accomplished Material Scientist with research and professional expertise in developing innovative materials solutions. As a ...
Doctor in Engineering specialised in medical devices research and development. Focused on validation and verification of development processes ...
Project Management | Stage-gate product development process for NPD - Medical Devices | Design for manufacturing (DFM) | Product compliance for...
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