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ATRIMED
Bangalore, Karnataka
Manufacturing Facilities
Pharma Manufacturing
Frequently Asked Questions
Third-party manufacturing allows a company to outsource its product production to a certified manufacturer. The products are then produced under the contracting company’s brand, leveraging the manufacturer’s facilities and expertise.
Launching a third-party manufacturing business typically involves:
- Creating a detailed and viable business plan.
- Registering your company legally under the Companies Act.
- Acquiring a valid Drug License.
- Obtaining a GST registration for your firm.
Before production, you must meet the manufacturer’s Minimum Order Quantity (MOQ) and provide key documents, including your GST registration and Drug License.
In third-party manufacturing, the vendor may produce for multiple clients simultaneously. Contract manufacturing, however, binds the manufacturer to serve only one client exclusively for a specified duration.
You’ll need to supply:
- A signed manufacturing agreement.
- Company and office address details.
- Identification documents (PAN, Aadhaar).
- GST or sales tax registration.
- Brand logo and design specifications.
Manufacturing time usually ranges from 30 to 45 days, depending on order size, including:
- Formulation approval (5–7 days)
- Packaging and printing customization (10–25 days)
- Regulatory approvals (12–16 days)
- Shipping (2–5 days)
To finalize artwork, provide:
- Brand and product name
- Composition, packaging details, and manufacturing info
- Preferred color scheme and design layout
- Company logo, name, and address for labeling
Yes, all certified pharmaceutical manufacturers maintain production and testing facilities that comply with industry standards and regulatory guidelines.
Common certifications include GMP, GLP, ISO, HACCP, and WHO standards to ensure quality and regulatory compliance.
Yes, manufacturers have a Minimum Order Quantity (MOQ), which varies by company. Always confirm the exact MOQ with the chosen manufacturer.
While delays can occur if processes are poorly coordinated, efficient planning between production, packaging, and logistics typically ensures timely delivery.
Yes, most third-party pharma manufacturers in India provide full packaging and labeling services as part of their offerings.
Formulation development is often included, but it is recommended to verify the scope of services with the manufacturer before signing a contract.
Certified manufacturers maintain dedicated quality control teams and follow strict testing procedures to ensure medicines meet regulatory and safety standards.