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UAE-based facility describes the process behind the making of sanitisers and the rising demand for sanitisers due to the COVID-19 pandemic.

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#coronavirus #COVID19 #handsanitizer
Transcript
00:00We are getting all the raw materials from all the brands which can be trusted at this
00:09particular time.
00:10There is nothing like shortcuts.
00:11All the chemicals has to be passed through QC, QA and micro as well because without the
00:15micro approval you cannot take any, any of the raw material inside the factory.
00:19So it has to be tested before it enters the factory only.
00:22So it will be in the loading bay before it comes to the factory.
00:24So there we will get the approval, then the loading, offloading and the rest of the procedure
00:27of the logistic will happen.
00:29Once the chemical will approve, that will come for the technical, like the development
00:32team which has recently developed all very nicely.
00:35They have done from last five, six, like two, three months, from last two, three months
00:39which they are doing.
00:40So they have recently done a very good job and because of that we are able to get the
00:44certifications from all around the world.
00:46We are trying to get it like UAE has given the first approval for our product.
00:50What our technical team has recently just upgraded from our lab basis to commercial
00:55basis in last few months.
00:56Once the corona has started spreading, we have started taking our production from 24
01:007, like from 12 hour shift to 24 hour shift and we are running continuously only three
01:04lines.
01:05We have only completely six to seven lines.
01:06We are continuously, we are doing the sanitizer production.
01:08Once we get the raw material cleared from the quality QC and micro, so it will come
01:12to the production as, as required for the technical specifications and the requirement
01:17of the cattle.
01:18So it comes to the production and then we do the manufacturing.
01:20I will just give you a glimpse of how we do the manufacturing.
01:23See there is a gelling agent and there is a vehicle and there is an active.
01:27So we first make the gel and then there is a vehicle.
01:29So we just mix both the things and then we add some additives in that.
01:33So when I say gel, gel is the vehicle here and the actives when I say, it's the IPA which,
01:39which is actually approved by USFD as the most impact material today on the viruses.
01:44So that is a major part there and this is the way how we are doing the manufacturing.
01:48There's a little mixing and all, a small stuff is there of mixing and all and it will directly
01:52go to the filling line where I say that there's a primary packaging, secondary, tertiary and
01:56quarterly is there.
01:57So the primary packaging will happen where there's no human intervention.
02:01Once the manufacturing is done, it will directly pass into the machine and automatically it
02:04will be sealed off and the final packaging will happen.
02:07From there again it will go to quality control and quality assurance and micro.
02:11Till they approve the product, it cannot go to the market before the approval of microbiology
02:16first.
02:17Sterling perfume industries are currently trying to be in the top most for the social
02:21cost to provide sanitizers as it's one of the best thing which WHO recommends for the
02:26world or for everybody to be used in a regular basis.
02:30So currently we are doing the manufacturing of around 200,000 pieces per day in all forms
02:36like 65 ml, 200 ml, 500 ml, 1 litre as per the consumer requirement and also in the cans
02:42we are in the market and we are trying to reach by 300,000 pieces a day to reach maximum
02:47volume of UAE as far as UAE and around the world where we can reach.
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