Quality & certifications

The studies performed by KYMOS are conducted under the internationally accepted quality standards, following the guidelines issued by ICH, EMA, FDA and other relevant Health Authorities. Kymos is under EMA regulatory domain and it is periodically inspected by the Spanish Medicines Agency (AEMPS). In July 2017 Kymos has been inspected by the FDA. KYMOS has a Registered Agent in front of the FDA and it is included in the self-identification list and GDUFA list. Our FEI number is 3008661256. The company has a Compliance & Quality Department taking care of the fulfilment of such guidelines and the Quality Policy of the company. Quality Control Managers are available to supervise the activities related with Batch Testing of our clients and Qualified Persons are available to certify the activities related with Batch Release. If you are interested in KYMOS services we are opened to fill your quality certification form or to be inspected by your QA department.

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Forum Auditorias

GMP Audit Certificate

Lebanon Ministry of Health

Lebanon Reference Lab for Biologics

Kymos Pharma Services GLP Certificate

GLP Certificate

Kymos Pharma Services GMP Certificate

GMP Certificate

Kymos Pharma Services Manufacturers & Importers Authorization Certificate

Manufacturer´s & Importer´s Authorization

FDA logo

FDA Inspection (EIR letter)

Kymos Pharma Services CIR Certificate

Crédit Impôt Recherche

SME stamp

Innovative SME stamp