Third Party Pharmaceutical Manufacturing
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Explore Core Manufacturing Capabilities
Select an operational division below to inspect cleanroom technology, regulatory standards, and packaging controls.
Formulation Development
Precision formulation development for immediate-release, sustained-release, enteric-coated tablets, and stable suspensions complying with IP, BP, and USP standards.
4-Step Contract Manufacturing Process
Click any stage to inspect technical validation parameters, testing protocols, and batch sign-offs.
Requirement
Product composition analysis, target market parameters, dosage selection, and tentative batch size estimation.
Dosage Form Capabilities & Packaging Options
Validated commercial production lines complying with cGMP standards and cleanroom environmental controls.
Tablets
Capsules & Softgels
Liquid Orals & Syrups
Ointments & Creams
Injectables & Drops
Powders & Sachets
Fast Turnaround
First orders in 20-25 days; repeat batches produced and dispatched within 12-15 days.
DCGI Approvals
Over 500 formulation licenses ready for private label manufacturing under your brand name.
Batch COA Assurance
Every release accompanied by certified laboratory testing records and validation.
Simple 4-Step Commercial Partnership Workflow
A transparent 4-stage onboarding protocol designed for pharmaceutical brand owners and distributors.
Requirement
Share your formulation specifications, desired packaging, and volume projections.
Discussion
Transparent cost estimate, cylinder design approval, and technical feasibility alignment.
Formulation & Production
Cleanroom batch execution, analytical validation, and blister packaging in 20-25 days.
Quality Delivery
Dispatch accompanied by certified batch COA with doorstep transit tracking.
Frequently Asked Questions
What documents are required to start Third Party Manufacturing?
To initiate contract manufacturing, you need: (1) Drug License Copy (Form 20B & 21B), (2) GST Registration Certificate, (3) Company PAN Card, (4) Brand Name Non-infringement Undertaking, and (5) Approved Artwork / Logo design.
What is the standard turnaround time for the first batch?
The initial order turnaround time is 20 to 25 business days (including foil cylinder engraving, artwork verification, and raw material validation). Repeat orders are dispatched within 12 to 15 business days.
Do you provide Certificate of Analysis (COA) for every manufacturing batch?
Yes. Every finished batch is tested by our QC analytical department and dispatched with an authorized Certificate of Analysis complying with pharmacopoeial monographs.
Launch Your Pharmaceutical Brand with Sygnus
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Contract Manufacturing Lead Form
Direct Quotation