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105 days ago
Take a premium advantage of MAVEN's Premium Organizational Management Services. These services ar...
171 days ago
We provide best AMC service where we take complete charge of ensuring regulatory compliance of al...
191 days ago
Get your Design History File planned and approval for your medical devices in Vietnam, Malaysia, ...
A clinical development plan is a subpart of a clinical evaluation plan which aims at the devices ...
A Clinical Evaluation Plan is a document that outlines the systematic process of assessing the sa...
178 days ago
Medical devices in Vietnam are classified by CDSCO, Central Licensing Authority. Medical device o...
The MHRA Registration database contains manufacturer name, address, MHRA reference (account) numb...
338 days ago
Get the EUDAMED registration done for IVD based on the regulations of EU 2017/746. We assist you ...
The risk management standard ISO 14971:2019 is the Holy Bible for medical device risk management....
330 days ago
It has been said that European Medical Device Regulations is the most significant change to the r...
325 days ago
Seeking trusted Biomass Pellets Export Companies in India? Look no further than 73 Deals! We are ...
However, the new medical devices regulations (EU MDR) contain important improvements including a ...
The interrelationship between EN ISO 14971:2019/A11:2021 and the General Safety and Performance R...
294 days ago
The CE mark is of utmost importance in the European market, and understanding its intricacies is ...
415 days ago
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354 days ago
We help you find the valid UK Responsible Person who is legally placed in UK market and help you ...
347 days ago
Our consultancy helps you in establishing your products in various countries with help of our exp...
344 days ago
Maven helps you to design a Stability Studies of Medical Devices Plan and reduce errors. The purp...
343 days ago
We help you get done medical devices usability testing. We provide medical device usability testi...