Escentia GmbH

medical devices

About

The go-to medical device safety and performance experts. Supporting the medtech industry globally, we help our clients maintain compliance in an ever-changing regulatory landscape. Escentia is a German-based, multi-lingual, Clinical Affairs consultancy. We deliver regulatory and compliance solutions to the medical devices industry. The name might be new to you, but we have a solid pedigree in the industry. From start-ups to large corporations, our experience of working in different businesses helps us to adapt to any challenge. No project is too big. No project too small. So whether it's a clinical strategy for a new product or an update to the clinical evaluation of a legacy product, we're ready to help. Our team of experts work within your processes or support process change where necessary to ensure best practice when drafting technical documentation. We'll then help you close the gap between the technical requirements and the clinical application.

Technologies

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Keywords

medical device regulation clinical evaluations cep cer postmarket clinical followup meddev 27 1 rev 4 postmarket surveillance medical equipment manufacturing clinical/medical research support supporting early clinical development medical device compliance medical devices risk management according to iso 14971 clinical research medical device safety services state-of-the-art reviews clinical evaluation clinical data collection other scientific and technical consulting services clinical strategy development regulatory documentation optimization regulatory support post-market activities mdr compliance safety cockpit for risk management risk management consulting regulatory documentation supporting legacy device evaluations

Location

2 Simeonscarre, Minden, North Rhine-Westphalia, Germany, 32423

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