Process of Third-Party Manufacturing at Mediboon Pharma

First let’s understand what third-party pharmaceutical Manufacturing means, The outsourcing of pharmaceuticals or items created from other manufacturing units with your own brand name is referred to as third parties or contract manufacturing. Currently, all marketing organizations have a highly popular strategy.

  1. Third-party manufacturing of over 500 Products.
  2. WHO-GMP certified pharma manufacturing facilities.
  3. Products portfolio of over 500 Products.
  4. Best Product Packaging in the Industry.

Third Party pharma manufacturing

Benefits of 3rd Party Manufacturing Pharmaceuticals at Mediboon Pharma

The hiring of a 3rd Party Manufacturing Pharmaceuticals is an excellent means of reducing the stress and load associated with the production process. It reduces manufacturing costs and completes the order placed with the desired efficiency at the necessary time.

3rd Party Manufacturing is used for a firm or company that produces its items under its own name by other manufacturers. It is a terrific way to complete the production process especially for those organizations that are modest in size and in their development phases.

Following are some factors that help you better understand, why third-party manufacturing companies are beneficial.

  • WHO-GMP CERTIFIED: Mediboon Pharma offers WHO-GMP Certified Products to its customers. Mediboon pharma is among the best pharma manufacturing companies in India.
  • VAST EXPERIENCE: With vast Experience, Mediboon Pharma is the best option when it comes to third-party manufacturing. Mediboon pharma has gained immense reputation in third party pharma manufacturing industry.
  • QUICK SERVICE: With a turnaround time of fewer than 30 days, Mediboon pharma is the way to go if you are looking for third-party manufacturing pharma companies with fast service.

6 Simple Steps of Third-Party Manufacturing in Pharma/Medicine Manufacturing

Steps of Third-Party Manufacturing in Pharma

  1. Choose Products and Prices: Choose the products you want to produce with your own brand names. Shortlist of probable suppliers – online, forwarding, etc. Please email/call them for a quotation, including Product Cost, Production expenses, securities, minimum delivery schedule quantities.
  2. Composition and Order Quantity Finalized: The order quantity of the product chosen should be finalized. At the conclusion of the order amount, the composition as specified by the manufacturer must keep in mind minimum order quantities.
  3. Purchase order Increase: You should acquire an order from the selected manufacturer after completion of the composition and order quantities for contract production. The manufacturer should also be asked to validate your items. A partial advance to commence the process should be deposited after confirmation.
  4. Designing & Packaging: You should fulfill all the steps for registration requested by the manufacturer once you have submitted an application. Your design work should be finalized as quickly as feasible. Key checkpoints when the artwork is completed: Check the name of the brand on board & foil, Packaging, Composition, Details of manufacture, Design & color, Marketing By firm name, logo & address on board & foil.
  5. Submission of Documents: Director of Company Profile (Aadhar Card and Pan Card), Authorized Resolution Signing Card for Processing Drug Registrations Tax / TIN Registration, Certificates Manufacturing Agreement, and Non-Commonwealth Certificate.
  6. Finally, Get the  Goods Delivery: After manufacturing the medicines, a quotation will be received indicating the details of the product production and the balance to be placed. After submitting documentation & clearing accounts, the products will subsequently be dispatched by your selected carrier.

FAQs (Frequently Asked Question) for Third-Party Manufacturing in Pharma

third party pharma manufacturing

Why should I Choose Mediboon Pharma for third-party manufacturing?

Mediboon Pharma provides pharma third-party manufacturing of over 500 products and covers all major therapeutic segments. Our pharmaceutical contract manufacturing is done in ISO 9001:2015 Certified plants.

Before starting the process of third-party contract manufacturing, we have to finalize the order quantity and composition of the product. While concluding the order quantity, we have to keep in mind minimum order quantities for the composition. For tablets and capsules, MOQ is usually between 500 – 1000 Boxes, i.e., 50000 – 100000 tablets. While finalizing we have to check if the manufacturer has approval for that composition.

After finalizing composition and order quantities for contract manufacturing. We will raise a quotation which will include all the costs that you will incur. A quotation includes the cost of the product, packaging material, securities if any in case of smaller batches. It also includes any other charges that you would have to pay for the contract manufacturing process.

To get a product made you need several documents. Some basic documents include a Drug license and GST number. In some cases, you will also require registration documents from your firm or company. DL is issued by your local Food and Drug authorities. DL is of 2 types, one for retail and the other for wholesale. GST number is issued by the Government of India and is required for Third party manufacturing. In some cases, some other documents like NON RESEMBLANCE CERTIFICATE are needed.

Promotional materials are used in everyday sales by medical representatives. They are the main marketing tools provided by companies to the franchises free of cost to promote the products. Promotional materials are the most proven marketing strategy. Some Pharmaceutical companies provide promotional material free of cost to their associates so that they can enjoy a powerful brand and professional image in the market. Pharma companies offer various promotional materials to support their franchise, such promotional tools.

GMP stands for Good Manufacturing Practices. There are certain quality standards set in GMP the production unit having the GMP certification, has to follow the guidelines set by GMP while manufacturing. GMP is a system that ensures the product is constantly produced and controlled according to quality standards. GMP covers all the aspects of production from starting material to the hygienic staff. WHO stands for World Health Organization. It is a specialized agency of the United Nations that is concerned with international public health. Like GMP in WHO, there are also some set quality standards which the manufacturing unit has to maintain while manufacturing the products. The quality standards of the WHO are stricter than GMP. WHO system ensures that products are produced and controlled according to the set guidelines.

It usually takes more than a month or so.