We stand for digitisation in the pharmaceutical industry
We ENABLE pharma manufacturers to have a smooth journey in digitisation.
Contact UsWe ENABLE pharma manufacturers to have a smooth journey in digitisation.
Contact UsWe at Enabl3, will enable, hand-hold and support YOU to digitise your end-to-end shop-floor related processes – from goods receipt of your raw materials, through all intermediary manufacturing and packaging stages, right up to final shipping.
We are specialists for development, design, execution & validation of the electronic batch record for the pharmaceutical industry.
Enabl3 is a focused company and concentrates on a very niche segment.
In short, we ENABLE pharma manufacturers to have a smooth journey in digitisation.
Enabl3 DOO holding is headquartered in Belgrade, Serbia with subsidiaries - Enabl3 GmbH in Cologne, Germany, and Enabl3 Systems Consulting Private Limited, Pune, India.
Enabl3 is an organization with energetic and highly skilled consultants and designers.
Our goal is to offer our customers the best possible advice in digitalizing their manufacturing processes. For them to attain the “smart electronic batch record of the future” - and to accomplish that, we are at their side from the first step, to implementation through to onward connectivity.
About UsOur team has vast experience in the deployment of MES solutions around the globe.
We are motivated and thoroughbred MES (Manufacturing Enterprise Systems)/MOM (Manufacturing Operations Management) consultants with niche expertise in the regulated pharmaceutical Industry.
We are working with major pharmaceutical giants, providing harmonised global core solutions that are applicable across multiple sites. We also provide special custom-tailored solutions for small single sites.
We have successfully deployed within the different types of manufacturing environments, namely, Biologicals, Solid dosage forms, Sterile forms, Packaging and also chemical API production.
What sets us apart is that we offer you best practices and generic template-based solutions that are easily scalable across your entire product portfolio, without compromising the essential stringent quality GmP regulations.
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