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Português
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I will write regulatory documents for medical devices
Biological and Biomedical Sciences
Hi,
Thank you for visiting my profile. I completed my MS degree in Biomedical Sciences in 2020.
Since then, I have worked as a medical writer and a visiting faculty for biology.
I have two publicati...
Nível 1
Atendeu a determinados critérios de desempenho e demonstra forte potencial no marketplace.
Sobre este Serviço
I will provide medical device regulatory documents which will comply with all the regulations laid out by the EU or FDA. I will also revise an existing medical document or report as per the criteria if the device's intended purpose has been changed. Moreover, I will also write and summarize the biological and clinical evaluation reports (a prerequisite of the medical device regulations - MDR ) of your given device. I will use the following sources (but not limited to) for skimming through the published literature on related medical devices:
- PubMed
- Google Scholar
- Cochrane library
I can also write a risk analysis or MDR reporting document according to the MDR regulation of your jurisdiction.
Tipo de Documento:
Documentação
•
Relatórios
Setor:
Médico e biotecnologia
Idioma:
Inglês
Preferência de estilo de entrega
Informe o freelancer sobre suas preferências ou preocupações em relação ao uso de ferramentas de IA na conclusão e/ou entrega de seu pedido.
Perguntas frequentes
Do you classify the devices into class?
I can do it but it's better that you provide this detail as the report is based on the device's classification
Are your prices fixed for the projects as mentioned in your gig?
No, the prices may vary depending up on the type of work you require.
Avaliações
4 avaliações deste Serviço
| (4) | ||
| (0) | ||
| (0) | ||
| (0) | ||
| (0) |
Classificação detalhada
- Nível de comunicação do freelancer
- Recomendar a um amigo
- Serviço conforme a descrição
Ordenar por
Mais relevante
I ibra0830
Estados Unidos
Highly recommend for any regulatory documents for medical devices
Até US$ 50
$
1 dia
Tempo
Útil?A 
adammurday
Canadá
Maria was very efficient and knowledgable about FDA regulations and processes. She was attentive and always quick to respond to requests. I absolutely recommend her and look forward to working together again in the future.
Útil?M mja_2022
Estados Unidos
She was great every step of the way, and even went above what was asked in making sure that the work was up to perfection. I will definitely be using her more for other projects.
Útil?A annubaby300
Cliente recorrente
Reino Unido
The work on risk analysis was really good. carried out the work better than expected and completed it even before the given time
Útil?
Avaliações
4 avaliações deste Serviço
| (4) | ||
| (0) | ||
| (0) | ||
| (0) | ||
| (0) |
Classificação detalhada
- Nível de comunicação do freelancer
- Recomendar a um amigo
- Serviço conforme a descrição
Ordenar por
Mais relevante
I ibra0830
Estados Unidos
Highly recommend for any regulatory documents for medical devices
Até US$ 50
$
1 dia
Tempo
Útil?A adammurday
Canadá
Maria was very efficient and knowledgable about FDA regulations and processes. She was attentive and always quick to respond to requests. I absolutely recommend her and look forward to working together again in the future.
Útil?M mja_2022
Estados Unidos
She was great every step of the way, and even went above what was asked in making sure that the work was up to perfection. I will definitely be using her more for other projects.
Útil?A annubaby300
Cliente recorrente
Reino Unido
The work on risk analysis was really good. carried out the work better than expected and completed it even before the given time
Útil?
