Third Party Pharma Manufacturing in India
Vibcare Healthcare is a compliance-led pharmaceutical contract manufacturing partner for brand owners and pharma marketing companies. We manufacture Tablets, Capsules, Oral Liquids, and External preparations with structured quality systems, documentation discipline, and scalable execution.
Manufacturing Capabilities and Dosage Form
We manufacture multiple dosage forms under structured quality systems. Below is a quick snapshot of our capabilities and indicative annual capacity by section.
Tablets
High-volume tablets with consistent batch quality.
3.5 Billion
Capsules
Repeatable batches with controlled QC release.
1.2 Billion
Oral Liquids
Stability-first manufacturing controls.
80 Million
Externals / Ointments
Creams & ointments with uniformity.
25 Million
Why Choose Vibcare Healthcare?
When you outsource third-party pharma manufacturing, the real risks are delays, inconsistent batches, weak documentation, and unclear accountability. Vibcare Healthcare is built to reduce those risks with compliance-led operations, clear communication, and scalable production.
Faster Turnaround Times
Lean planning and controlled workflows reduce avoidable delays—so your launches and replenishments stay on track.
Market-Ready Packaging
Modern packaging options with clean execution—helping your brand look credible, consistent, and shelf-ready.
Rigorous Quality Control
Every batch passes through stringent in-process and post-process QC testing in our fully equipped labs.
Documentation You Can Defend
Clear batch documentation and COA-aligned release support—built for brands that care about audits and credibility.
Scalable Capacity, Flexible MOQs
From smaller initial runs to high-volume repeat production—your growth doesn’t require changing manufacturers.
Transparent Partnership
No vague commitments. Clear communication, ethical practices, and defined responsibilities from RFQ to dispatch.
What Is Third Party Manufacturing?
Third party manufacturing (also called pharmaceutical contract manufacturing) is a business model where a brand owner or pharma marketing company gets medicines manufactured at a licensed, compliant facility—under an agreed scope, specifications, and quality responsibilities.
In simple terms: You own the brand and market access; we manufacture under a controlled quality system and support documentation and packaging execution as per the agreed requirements.
Who typically uses third party pharma manufacturing?
- Pharma marketing companies (PCD / institutional / distribution-led)
- Brand owners expanding portfolios without investing in a plant
- Businesses scaling volume while maintaining batch consistency
- Companies requiring a reliable third party medicine manufacturer for repeat supply
Why brands choose it
- Faster product rollouts and portfolio expansion
- Reduced capex and operational complexity
- Access to compliant manufacturing systems and quality controls
- Ability to scale without changing vendors repeatedly
How It Works (Process / Timeline)
A clean contract manufacturing engagement succeeds when responsibilities are defined early and execution is structured. Here is the typical flow we follow:
Phase 1: Planning & Feasibility
Requirement Capture (Day 0–1)
You share basics: Dosage form, Composition, Packaging format, and Target volumes.
Feasibility Review (Day 1–3)
We evaluate manufacturing fit, packaging stability, timeline assumptions, and documentation scope.
Quotation + Alignment (Day 2–5)
You receive a structured proposal with pricing, lead times, and a next-step checklist to avoid delays.
Documentation & Artwork (Week 1)
We align on master specifications, artwork/label inputs, and final production plans. (NDA stage).
Phase 2: Execution & Delivery
Planning + Procurement (Week 1–2)
We lock the production slot, batch plan, material/pack readiness, and quality checkpoints.
Manufacturing (Week 2–4)
Production executed with in-process checks and controlled documentation for consistency.
QC Testing + Release (Week 3–5)
QC testing aligned with agreed scope (COA) so dispatch isn’t delayed by gaps.
Packing + Dispatch (Week 4–6)
Final packing, dispatch coordination, and post-dispatch support for planning.
Note: Timelines vary by dosage form, packaging complexity, batch size, and readiness of inputs.
Frequently Asked Questions
Everything you need to know about our third-party manufacturing process.
What is the difference between third party manufacturing and contract manufacturing?
In pharma, the terms are often used interchangeably. In a strict compliance sense, it’s about a documented agreement and defined responsibilities for manufacturing/testing and quality events.
Do you sign an NDA before sharing details?
Yes. For serious projects, NDA-first is recommended before exchanging sensitive formulations, vendor details, or commercial inputs.
What dosage forms do you manufacture?
Tablets, Capsules, Oral Liquids, and External preparations (creams/ointments, etc.).
Do you help with packaging?
Yes—packaging coordination is part of execution, aligned to your product requirement and positioning.
What documents will I receive?
Typical outputs include batch-related documentation and QC outputs as applicable (e.g., COA format), aligned to GMP documentation expectations.
What is your MOQ?
MOQ depends on dosage form, pack style, and batch planning. Share your target pack and forecast; we’ll confirm feasibility.
How do you ensure product quality?
GMP emphasizes defined and documented processes for production and testing and suitability of personnel/premises/materials. Our execution is designed around that discipline.
Do you support audits?
We support compliance discussions and audit-readiness pathways appropriate for contract manufacturing relationships (scope defined case-by-case).
Can you manufacture for pan-India distribution?
Yes—dispatch planning can be aligned to your distribution model.
Can you manufacture under my brand name?
Yes—third party manufacturing is commonly executed for marketer/brand-owner labeling requirements, within the compliant framework.
Do you manufacture new product development (CDMO)?
We can guide whether your requirement fits standard contract manufacturing or needs a development-oriented CDMO approach. (A dedicated CDMO page is recommended for this topic.)
How do I start?
Use the RFQ form. Share dosage form, composition/strengths, packaging preference, and your target volumes.
