Results for “dry syrup third party manufacturing”
Frequently asked
What is pharma third party manufacturing?
Third party (contract) manufacturing means a licensed, WHO-GMP certified manufacturer produces medicines under your brand name. You own the brand, the marketing and the sales; the manufacturer handles the facility, the licences, quality testing and packing to your artwork.
What is the minimum order quantity (MOQ) for dry syrup third party manufacturing?
MOQ depends on the dosage form and the manufacturer. As a guide, tablets and capsules usually start around 25,000–50,000 units per product, liquids at about 3,000–5,000 bottles and injections at 5,000–10,000 vials or ampoules. Ask each shortlisted manufacturer for their exact MOQ and batch size.
Which documents do I need to get products manufactured?
A drug licence (wholesale), GST registration and a trademark application or registration for your brand name. The manufacturer uses its own manufacturing licence (Form 25/28) and product permissions from the state drug controller.
How long does the first batch take?
Usually 25 to 45 days after the order, artwork approval and advance payment — longer if a new product permission or a new packing material has to be arranged. Repeat batches are typically faster.
Is it free to contact manufacturers on Third Party Manufacturers?
Yes. Buyers never pay on Third Party Manufacturers. Send your requirement to as many manufacturers in India as you like and compare their rates, MOQ and certifications before you decide.
