Inquiry Roundup- Medical Devices

I am working on a project that aims to measure optical density ratio’s in images obtained from a very popular eye device names Optical Coherence Tomography (OCT), all images have been extracted in the same manner from this device, we aim to measure optical density ratios of the subretinal fluid to supraretinal fluid, the retinal nerve fiber layer and retinal pigment layer Using ImageJ, the methodology has been described previously in the following papers: 1-Longitudinal optical density analysis of subretinal fluid after surgical repair of rhegmatogenous retinal detachment. http://www.ncbi.nlm.nih.gov/pubmed/25077533 2- Optical density ratio in the subretinal fluid: differentiating chronic central serous chorioretinopathy and polypodial choroidal vasculopathy. http://www.ncbi.nlm.nih.gov/pubmed/25447112 3- Optical Density of Subretinal Fluid in Retinal Detachment. http://www.ncbi.nlm.nih.gov/pubmed/26284548 Please review and comprehend before submitting a response, we aim to evaluate optical density of the subretinal fluid in specific condition and compare it to controls .Thanks
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Our medical device company is interested in studying the feasibility of transmitting data using piezoelectricity. We are looking for a Piezoelectricity Scientist or Piezoelectricity Expert for a potential project.

We are looking for individuals who have a background in physics, engineering, and sonar and data communication.

Please respond with your CV and your qualifications.
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Greetings, I am writing regarding detailed information on medical devices and medicinal products regulatory information in the following countries: Kuwait, UAE, Jordan , Lebanon , Iran , Turkey and Tunisia.
1. Who can be Marketing Authorization Holder (e.g. German–based or locally based company)?
2. What are the requirements a company must fulfil in order to be assigned as MAH?
3. How does a change of the Marketing Authorization Holder is regulated in these countries
a) Type of process?
b) How long does the process take?
c) Are there any differences in the process if a MAH is changed during registration or post- approval?
d) Are there any additional conditions which we have to consider?
4. How does a change of the Distributor/distribution partner is regulated in these countries:
a) Type of process?
b) How long does the process take?
c) Are there any differences in the process if a MAH is changed during registration or post-approval?
d) Are there any additional conditions which we have to consider?

Anticipating a prompt response on the same

Thanks in advance.
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