Certifications
Our intention is to always adhere to the highest standards of pharmacovigilance, including but not limited to, European certificates of conformity with EU norms such as G.M.P certification, WHO certified bioequivalence studies, ISO9001, ISO13485:2003 and EN ISO 13485:2012, ICH Q8. ICH Q9. ICH Q10.
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Our main objective is supplying medical goods that are safe and secure for individual consumption, hence why we place such a strong focus on ensuring product quality.
Following and upholding the strictest standards ensures that our commitment to our quality objectives are met in accordance with the law, irrespective of the country where we operate.
All our products are manufactured by industry certified personnel who possess decades of experience in the handling and processing of medical products and equipment.
In addition, Natrelle Pharma ensures all single use consumables and medical devices meet the requirements of the Medical Devices Directive 93/42/EEC, MHRA, EMA, INVISA, CECMED and ANVISA.