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Upgrade QMS 13485:2013 to ISO 13485:2016

€50-1500 EUR

Completed
Posted over 4 years ago

€50-1500 EUR

Paid on delivery
Hi We are looking for a trained professional who can - help us upgrade our current QMS 13485:2013 to ISO 13485:2016 and to train and prepare us for MDSAP audit - help us upgrade Technical file(s) - Update the clinical evaluation (we don't expect to find all of these qualities in one person of course). Bye Nevada
Project ID: 18814063

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6 proposals
Remote project
Active 5 yrs ago

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Hi Nevada, I am an Australian technical writer who has worked on ISO projects in the past particularly for quality management systems. Do you have a copy of ISO 13485:2016? I can also take a look at your technical files and possibly upgrade them as well. It depends on what they are and what you need.\r\n\r\nWith more than 20 years experience as a technical writer, I have worked with companies such as Raytheon Australia and BAE Systems. Although not medical, I have worked on medical projects in the past. Since then I have worked on countless freelance projects with success. Please see my portfolio and reviews.\r\n\r\nI invite you to open a conversation abut your project requirements.\r\n\r\nThank you
€70 EUR in 20 days
5.0 (3 reviews)
3.3
3.3
6 freelancers are bidding on average €939 EUR for this job
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Hello, I'm a medical writer. I focused on providing great content on medical related topics. I have done this for years. My experience and skills in writing will help work on that aspect of clinical evaluation update mentioned in the job description.
€750 EUR in 5 days
4.9 (8 reviews)
4.3
4.3
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Hello , i am a qualified pharmacist working in France . Error being hardly acceptable in the patient management , the organisation of health care centers must be constantly improved . We health practitionner in france are trained to ensure good quality practices ( i have a certification ) , and it would be of a great pleasure to help you in that process . For example I participated in the making of a process to make sure the patient's prescription is not modified upon ER entrance .
€1,200 EUR in 20 days
0.0 (1 review)
0.0
0.0
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Hi How are you? I can help with parts of your project.... I have many years experience in the medical device industry, in roles such as; quality systems, risk management. I am a certified lead auditor for ISO13485:2016 and have a certificate in medical device risk management (certificates can be provided on request). I am also knowledgeable on the requirements of MDR2017/745 and clinical evaluation and technical file requirements of this regulation (I'm not familiar with regulatory requirements of countries adopting MDSAP; just Europe). Please don't hesitate to contact me if you would like to chat about this project as I would be very interested. Thanks Stephanie
€1,111 EUR in 28 days
0.0 (0 reviews)
0.0
0.0

About the client

Flag of NETHERLANDS
Breda, Netherlands
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Member since Feb 26, 2019

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