Quality & certifications

KYMOS projects are conducted in accordace with the internationally accepted quality standards, following the guidelines issued by ICH, EMA, FDA and other relevant health authorities. Kymos falls under the EMA's regulatory umbrella and is periodically inspected by the Spanish Medicines Agency (AEMPS). In July 2017, Kymos was inspected by the FDA. KYMOS has an FDA Registered Agent and is on  the self-identification list and GDUFA list. Our FEI number is 3008661256. The company has a Quality Department in charge of ensuring both these guidelines and the company's quality policy are followed. Quality Control Managers are available to supervise batch testing activities and Qualified Persons are available to certify the Batch Release activities. If you are interested in KYMOS' services, we are open to filling in your quality certification form or being 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 (VAI letter)

Kymos Pharma Services CIR Certificate

Crédit Impôt Recherche

SME stamp

Innovative SME stamp