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WHO GMP Certified Third Party Manufacturer – Lifevision Chandigarh is one of India's leading WHO GMP Certified Third Party Manufacturers. In India, we manufacture safe and high-quality pharmaceutical items. All products are delivered on time and without interruption. Since our inception in 2010, the company has experienced rapid expansion in the pharmaceutical industry
As the most prominent third-party pharmaceutical manufacturing firm, our main goal is to supply customers with the greatest Active Pharmaceutical Components and formulations. Clients receive a constant supply of the entire product range with which they are concerned. Lifevision Chandigarh is a renowned maker of pharmaceutical products in India. Each of the company's medicines comes with detailed instructions so that clients are pre-informed about the medication.
India's sector of pharmaceutical contract manufacturing has been expanding rapidly owing to the country's status as a major manufacturer of affordable quality drugs. India leads in manufacturing and supply of generic drugs with an estimated 20% share of the world’s exports of generic drugs and provides 55-60% vaccines to the United Nations Children Fund (UNICEF) as of May 2025. Additionally, India provides 99%
The numbers above are indicative of a robust system that is in place with regards to regulatory requirements. India has the most pharmaceutical factories compliant with US FDA requirements, outside of the US, and the sector has grown by a CAGR of 9.43% over the last nine years. You may learn about the pharmaceutical sector's current standing from the Department of Pharmaceuticals, Government of India.
It is this scale and level of regulation that make Indian contract manufacturing so appealing to new or developing pharma brands; all the necessary resources, standards, and skills are already available, making it unnecessary to develop capabilities from ground zero.
This is the single most important decision that pharma brand owners face before they launch. This is an honest comparison for you:
| Factor | Third-Party Manufacturing | In-House Manufacturing |
| Initial investment | Low - no facility setup required | High - facility, equipment, licensing |
| Time to market | 30 to 50 days are typical | 12 to 24 months for facility setup |
| Regulatory burden | Shared with the manufacturer | Fully owned by brand |
| Quality control | Manufacturer's QA/QC systems | Must build in-house QA/QC team |
| Scalability | Easy = order volume flexes with demand | Needs capital investment to scale |
| Best suited for | Startups, new brand launches, testing new products | Established brands with consistent high volume |
You’re at the right place if looking trying to enter the market as a new pharma brand owner or a PCD franchise company. You get the fastest and the lowest risk path with third party manufacturing which results in a compliant finished product.
A lot of brand owners have one common question in mind which is about what it actually costs to get started. Here is a general framework where exact pricing depends on the dosage form, batch size and packaging complexity:
| Dosage Form | Typical MOQ | Cost Driver |
| Tablets / Capsules | 50,000 to 1,00,000 units per batch | API cost, blister/strip packaging |
| Syrups | 5,000 to 10,000 bottles per batch | Bottle, cap and carton sourcing |
| Ointments / Creams | 5,000 to 10,000 tubes per batch | Tube material, filling line setup |
| Sachets | 50,000+ sachets per batch | Lamination film, sealing |
Contact Lifevision Chandigarh now to get a direct quotation. It should be based on your specific formulation, batch size and packaging needs.
All resources incorporated in our guidelines have been approved by accredited manufacturing units, demonstrating our commitment to the quality of the drug. To assure product quality, all raw ingredients utilized in the manufacturing of Pharma goods are purchased from reputed pharmaceutical vendors.
In order to ensure that the products matched worldwide standards, Lifevision Chandigarh uses emerging technologies and global procedures in pharmaceutical production facilities. Given that Lifevision Chandigarh is a third-party manufacturer with GMP accreditation. Furthermore, we have over 12 years of experience in the health sector. As a result, we provide our clients with a variety of business benefits.
Because we will give you the finest quality products, our production models make the whole procedure cost-effective for your business because you will not have to bother about startup investment, maintenance, or manufacturing units.
You will have the option to work with professionals and specialists who have been with us for years, as well as our colleagues and healthcare centers who have already joined our ranks, by partnering with our organization.
The GMP-WHO authorities have certified our production facilities. Additionally, the production facility is empowered with cutting-edge and technological advancements.
Third-party manufacturing firms provide services such as product delivery on time, sales, and marketing. Our Services provide you with a lot of freedom to come up with new marketing strategies.
By focusing on each area of the production stage, the third-party production company produces items in a short amount of time and space. Our manufactured items are earning international and universal praise all over the globe.
A third-party manufacturing company can help you expand your business with a low-cost investment. We make certain to offer the best item for our clients so that they can continue to flourish.
A WHO GMP Approved Third Party Manufacturer makes medical product production simple. The majority of start-ups take advantage of this enterprise; with minimal resources and succeed spectacularly. Furthermore, you will gain specific manufacturing knowledge that your in-house division cannot give. Lifevision Chandigarh is always there to be a part of your industrial exposure.
Location: Plot Number 11-12, Dainik Bhaskar Building, Sector 25-D, Chandigarh – 160014, India
Phone: +91 9915454503
Email: marketing6@lifevisionhealthcarechd.com
A - To obtain WHO GMP certification a third-party manufacturer must undergo a thorough inspection process that is carried out by qualified inspectors from the relevant national regulatory body or WHO. The facility's infrastructure, operating procedures, quality assurance procedures, and documentation standards are assessed for compliance with GMP standards during the inspection.
A - Some of the advantages include:
A - MAQs are different by dosage form. These are mostly 50,000+ units for tablets and capsules, 5,000 to 10,000 units for syrups and creams.
A - The full process mostly takes about 40 to 50 days for a new product. These include drug authorisation, packaging sourcing, production and shipping. Repeat orders where packaging and formulations are already established mostly take about 30 to 40 days.
A - WHO-GMP is actually specific to pharmaceutical manufacturing practice. This covers a facility design, process validation and quality systems.
A - Yes, substantially. Third party manufacturing avoids the capital cost of facility construction, equipment and licensing. This is a multi crore investment with 12 to 24 months of setup time.
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