SIMPLE STEPS FOR PHARMACEUTICAL THIRD PARTY MANUFACTURING IN INDIA
FOLLOW THE BELOW SIMPLE STEPS TOWARDS THE PHARMACEUTICAL THIRD PARTY MANUFACTURING PROCESS OF YOUR PRODUCTS
MINIMUM ORDER QUANTITY AND COMPONENT SELECTION
First, to start third party contracts for your product production, we must complete the minimum order quantity MOQ and product composition (salt names). After completing the order quantity, we will let you know the composition minimum order quantity and batch size. For tablets and capsules, this is usually between 500 and 1000 cartons, i.e. 50000-100000 tablets and injections; It is 1000-10000 vials. By selecting all of these factors, as we mentioned above, we need to check whether we have a salt production permit for this salts composition.
THE PRICE OF YOUR DESIRED PRODUCTS
After salt has been named and MOQ, we’ll send you a quote, which will include all the information and costs you’ll pay for your products. This will consist of product costs, packaging costs, securities or insurance, if any, in the case of very small lots. The offer will also include various fees that you would have to pay for the pharma contract manufacturing process.
To obtain actual products, you must submit some documents. Only a few basic documents are such as a drug license and GST number. Sometimes you have to submit a registration document for your company or company and you will need documents such as the NO CERTIFICATE of CONFORMITY. If necessary, we may ask you to cancel your company check, PAN card or Adhar card. Every time you plan to create a TPM, keep all your documents ready.
Design and packaging material
After the documentation we will start the process and we’ll send you a slightly different design, so you can choose the best product design to suit your needs. Once you have approved the design, it will be handed over to final printing of the package. We will print enough material for your articles to keep stock levels for the next order as this may be necessary for small batches.
MANUFACTURE OF THEIR PRODUCTS IN PLANT
The pharmaceutical world GMP means good manufacturing practice and can also be used in our factories. The GMP Compliance production unit, which has a GMP certificate, has certain quality standards and we must follow the guidelines of the GMP during production. We’ll ask for about 20-35 days to fulfill the entire requirement and deliver the products to your door. We ensure that the product is constantly manufactured and controlled according to quality standards. We cover all aspects of quality and production, from raw materials to finished products. Every time products are manufactured with the help of a qualified professional, the correct procedure/guidance must be followed at each stage.