Skip to main content

How to grow your Pharma Business?

  Growing a pharma business requires a strategic approach considering the specific context of your company and the pharmaceutical industry as a whole. Here are some general pointers to get you started: Market and Customer: Identify your target customer: Deeply understand the specific needs and challenges of your target audience, whether it's doctors, patients, hospitals, or other healthcare providers. This helps tailor your products, services, and marketing efforts. Focus on unmet needs: Look for gaps in the market where existing solutions are inadequate or unavailable. Addressing unmet needs can give you a competitive edge and drive innovation. Track market trends: Stay updated on regulatory changes, technological advancements, and emerging diseases to adapt your approach and anticipate future opportunities. Products and Services: Invest in R&D: Develop innovative products or differentiate existing ones through unique formulations, delivery methods, or combinations. Remember

How much investment required in third-party manufacturing and Loan License Manufacturing?


Today we will talk about a query. Query is that how much investment is required for third party manufacturing and loan licensing if started with 4 products?

Loan Licensing and Third Party, both are different

If we discuss in detail 
Loan licensing is what in which a pharmaceutical marketing company tie up with pharmaceutical manufacturing company and manufacturing company apply for issue for manufacturing license for marketing company in its premises that is applied at state drug control authority

That is like applying for new manufacturing license and that takes lots of investment because whole documents and process is to proceed from new way.
Plant, machinery and technical persons are used of manufacturing company and new manufacturing license is issued at marketing company name.

So, the manufactured by name is of marketing company also in loan license. Manufacturing name will be of marketing company in loan licensing. Only address is belonging to pharmaceutical manufacturing company. So, investment not only depend at products but initial investment also cost you lot.

If we talk about third party manufacturing concept, only you need to find for a third-party pharmaceutical manufacturing company who can provide you your marketed by product under your brand name at third party manufacturing basis.

You need to contact them and give your product detail that you want to manufacture and their brand name

If manufacturer already has approval of that ingredient/composition then it doesn't need to take approval but if manufacturer doesn't have approval, then it will take ingredient/composition approval from state drug licensing authority

Then manufacturer will design your products design and proceed further.

According to payment schedule and other term & conditions finalization, your products go into manufacturing process for finished goods.

In that case marketed by name and address will be yours and manufactured by name and address will be of actual manufacturing company.

Here you have to invest only amount as per cost of these four products only.

Investment requires for third party and contract manufacturing:

It is not fixed when we talk about investment or costing of product because some products are cheaper and some are expensive.

If you will get manufactured costlier product then your investment will go high and if those are cheaper then investment will be less

Suppose you get manufactured a product having cost 50 rs per box

and you get manufactured 500 boxes as minimum order quantity at third party manufacturing basis then this will cost you 500*50 = 25000 plus gst or freight included or excluded as finalized under term & conditions
So that will cost you 25000 plus gst

But if you have finalized a product having 600 rs per box and getting manufactured 300 boxes then this will cost you 600*300 = 180000 plus gst or freight included or excluded as finalized under term & conditions

So that's difficult to give idea how much investment you require to launch four products that depend at your products cost whether you are getting manufactured cheaper products or costlier products...

For cheaper products investment will be low and costlier product, it will be high.

It is better to avoid loan licensing in starting because you have to invest more at documents and licensing also

Some pharmaceutical manufacturing companies also charges monthly rent from marketing company for loan licensing because you are using its manufacturing facilities or they charge based on per pc or as per your tie-up that cost you more

But in third party manufacturing, you can avoid this so, you need to go for third party manufacturing.

And as per your products you can calculate whether they are cheaper or costlier and how much minimum order quantity, how much cost of your product, packaging charges if applicable or any security charges is applicable or not?

So, there are many factors

Calculate all and find out how much investment you require for getting manufactured your product at third party basis or loan licensing

Hope this information is helpful to you...

Comments

Ayurvedic Medicine Company

Send Distribution/Franchise Query

Name

Email *

Message *

Register your business at

Find pharmaceutical, cosmetics, nutraceutical, ayurveda and alternative medicine's distributors, franchise, suppliers query for free.

If you want to take distribution, franchise or associates with any pharmaceutical, cosmetic or ayush company then you can find it here...

Popular posts from this blog

What are the Schedules under Drug and Cosmetic Act, 1940 & Rules 1945?

Schedules are the set of provisions for classifications of drugs, forms, fees, standards, requirements and regulations related to pharmaceutical, Ayurvedic (including siddha), unani and tibb system of medicines, homeopathy, blood and realted products etc under Drug and Cosmetic Act, 1940 and Rules, 1945. The schedule to the drugs and cosmetics act are Schedule A, B, C, D, E, F, G, H, I, J, K, L, M, N, O, P, Q, R, S, T, U, V, W, X, Y. Drug and cosmetic rules are divided into schedules alphabetically and named also alphabetically like Schedule A, Schedule B etc till Schedule Y. The schedules to the drugs and cosmetics act are important part. Every schedule contains specific information as discussed below. Schedule A:  Schedule A  describes application forms and licenses types. Download Schedule A Pdf Schedule B:  Schedule B  describes Fees for test or analysis by the Central Drugs Laboratories or State Drugs Laboratories. Download Schedule B Pdf Schedule B1: Schedule B1 describes

State Pharmacy Council, Its Constitution and Composition and Functions

State Pharmacy Council: State Pharmacy Council is constituted as per the Pharmacy Act, 1948 & State Pharmacy Rules, 1951. State Pharmacy Council is an authoritative council to regulate Pharmacy Act, 1948 & State Pharmacy Rules, 1951. What is state pharmacy council? State Pharmacy Council means a State Council of Pharmacy constituted under section 19, and includes a Joint State Council of Pharmacy constituted in accordance with an agreement under section 20 under the Pharmacy Act, 1948 & State Pharmacy Rules, 1951. State Pharmacy Council constituted and work under  Pharmacy council of India . Composition of State Pharmacy Council: The State Pharmacy Council consists of the following: i) Six members, elected from amongst themselves by registered pharmacists of the State; ii) Five members, of whom at least three shall be persons possessing a prescribed degree or diploma in pharmacy or pharmaceutical chemistry or registered pharmacists nominated by the State Governme

Schedule F, F1, F2, F3, FF

Schedules:  Schedule A ,  Schedule B ,  Schedule C ,  Schedule D ,  Schedule E1 ,  Schedule F ,  Schedule G ,  Schedule H ,  Schedule H1 , Schedule I,  Schedule J ,  Schedule K ,  Schedule L1 ,  Schedule M ,  Schedule M1 ,  Schedule M2 ,  Schedule M3 ,  Schedule N ,  Schedule O ,  Schedule P ,  Schedule Q ,  Schedule R ,  Schedule S ,  Schedule T ,  Schedule U ,  Schedule V , Schedule W,  Schedule X ,  Schedule Y Schedule F: Schedule F (Rule 78 and Part X) describes requirements related to Blood and Blood Components. We are describing general heading about schedule. This will give you Idea about schedule structure and matter. Part XIIB: Requirements for the functioning and operation of a blood bank and / or for preparation of blood components. I. This section describes details about Blood Bank and Blood Components General Accommodation for a Blood Bank Personnel Maintenance Equipment Supplies and Reagents Good Manufacturing Practices (GMP’s) and Standard Operat