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YES is a leading provider for Regulatory Affairs. We are your partner for consulting, solutions and implementation.
Our experienced teams accompany your pharmaceutical products from the laboratory to the marketing authorisation and during its entire lifecycle.
We conduct custom-made procedures for marketing authorisation of veterinary medicinal products and thus offer access to global markets in no time.
YES Medical Devices Services GmbH has specialised itself in a strong network to meet your requirements.
Whether monitoring of the scientific literature, readability test or pharmacovigilance. We provide the online solution for your business.
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Literature search
DIA-Journal Abstract
All marketing authorisation holders are required to regularly monitor medical literature for suspected adverse drug reactions.
AMNOG - benefit
Clearing the hurdle
Does your innovative medicinal product have an added benefit according to AMNOG? We are specialised in the preparation of value dossiers and make sure that your product is safe and successful in the future.
ISO 9001
Certification of YES
We are delighted to be ISO 9001:2008 certified as of 07 February 2013.
YES - your Cosmetics
New EU regulation
The regulatory requirements for cosmetic products are becoming increasingly complex. Hand these tasks over to an experienced service provider. YES services for the cosmetic industry have been designed specifically for you. Thus, we find a customised solution for your inquiry.
Leading in Regulatory Solutions
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