FAQ
Frequently Asked Questions
CMO is defined as the process of outsourcing the work of manufacturing or
Contract Manufacturing Outsourcing (CMO) refers to the practice of subcontracting the production of pharmaceuticals, such as tablets and capsules, for consumption by third parties. This can encompass drug development and regulatory assistance to facilitate market release approvals.
The advantages include:
- Application of advanced expertise
- Global market access
- Cost-efficiency
- Ensured quality control
producing medication like tablets and capsules for third party consumption.This process may involve drug development processes and even regulatory support to help with the approvals required for a drug to release in the market.
- The benefits are :-
- 1. Use of advanced skills
- 2. Global outreach
- 3. Cost effectiveness
- 4. Quality assurance
Third-party pharmaceutical manufacturing involves the rebranding of pharmaceutical products or having them manufactured by another production unit under your brand name.
The advantages are as follows:
- Delivering top-tier products to partners.
- A cost-effective approach that makes pharmaceutical manufacturing affordable and budget-friendly.
- Ensuring a steady supply and offering deliveries well ahead of specified deadlines.
- Enhancing the reputation of both the business and its products.
- Facilitating business expansion opportunities.
Third-party manufacturing and contract manufacturing form the foundation of the pharmaceutical sector. With the increasing demand for medicines, manufacturing companies play a pivotal role in meeting this rising need.
Third-party manufacturing involves a pharmaceutical company sourcing medicines produced under its own brand name, at a predetermined quantity and specified time, from a manufacturing company. Typically, small to medium-sized companies opt for third-party manufacturing services, and there are minimal conditions or time constraints in this arrangement.
Contract manufacturing, on the other hand, occurs when a pharmaceutical company requests customized conditions, such as providing raw materials, packaging materials, and other product-specific requirements, to the manufacturing company. It involves a legally binding agreement in which the manufacturer commits to delivering the product on a predetermined date. Large companies often engage in contract manufacturing, offering technical insights to pharmaceutical firms.
The choice between contract manufacturing and third-party manufacturing is influenced by the specific needs of the company. As it can be extremely challenging for pharmaceutical companies to handle all operations independently, collaboration with external pharmaceutical companies proves to be the most cost-effective approach. These collaborations can encompass a wide range of activities, including product production, packaging, testing, and further product development.
Packing material refers to the external covering used to package doses, which can take the form of materials such as paper, plastic, tin, or rubber. Examples of packing materials include outer cartons, mono cartons, foils, labels, and laminated tubes. These materials are categorized as follows:
- BOX
- FOIL
- LABEL
- LAMI TUBE
- INNER/MONO CARTON
There are two primary procurement approaches:
Direct Involvement in Printing: This involves actively participating in the printing of packing materials.
Manufacturer Procurement: Alternatively, manufacturers can handle the procurement themselves. In this scenario, the manufacturer may provide pricing options on a third-party basis, either with or without the packing material.
The inventory requirements typically depend on the product’s cost and can vary from one product to another or from one dosage to another. Packing materials constitute a significant portion of the inventory, and for certain products, their cost may even exceed the total batch cost. Consequently, inventory prices may fluctuate.