Organic Pharmaceuticals Pvt. Ltd. offers comprehensive third-party and contract manufacturing services to pharmaceutical companies, healthcare startups, and established brands across India. Whether you need a single dosage form or a diverse product range, we provide end-to-end manufacturing solutions that meet your exact specifications.
Our Dadri facility โ located in India's largest pharmaceutical manufacturing cluster โ gives us significant cost and logistics advantages, enabling us to offer highly competitive pricing without any compromise on quality. We have successfully manufactured for 50+ brands and delivered millions of units annually.
All manufacturing arrangements are protected by robust NDAs and strict IP confidentiality protocols.
98.7% on-time delivery rate backed by robust production planning and dedicated order management.
Full regulatory documentation support โ COA, CoC, Batch Manufacturing Records, and Stability Data.
25,000 sq. ft. WHO-GMP certified plant with dedicated manufacturing areas for different dosage forms, fully compliant with Schedule M of Drugs & Cosmetics Act, 1945.
Strategic location in Dadri, combined with bulk raw material procurement and efficient operations, allows us to offer prices 15-25% below industry average.
In-house R&D team can develop custom formulations from scratch or optimize existing formulations to meet your market requirements, bioavailability targets, or patient preferences.
Expert regulatory affairs team assists with product registration, Form 44 applications, new drug marketing authorizations, and state drug controller approvals across India.
Full packaging customization including blister packs, strip packs, HDPE bottles, carton printing with your brand artwork. We manage the entire artwork and packaging supply chain.
Real-time production status updates, batch-wise quality reports, and detailed invoicing. Our client portal gives you full visibility into your manufacturing orders round the clock.
Our streamlined manufacturing process ensures your products are delivered on time, at the right quality, and within budget.
Share your product requirements โ dosage form, composition, pack size, and quantity. Our business development team responds within 24 hours with preliminary feasibility and commercial terms.
For new products, our R&D team develops trial formulations and runs stability studies. For existing formulations, we conduct a technical feasibility review to confirm manufacturing compatibility with our facility.
We execute a manufacturing agreement and NDA. Quality specifications, in-process control parameters, finished product specifications, and release criteria are agreed and documented in the Quality Agreement.
Raw materials (APIs and excipients) are sourced from approved vendors only. All materials undergo identity, purity, and assay testing per pharmacopoeial standards before use in manufacturing.
Production commences as per the approved Batch Manufacturing Record (BMR). In-process quality checks at every critical stage ensure batch consistency and compliance with approved specifications.
Every finished batch undergoes comprehensive QC analysis โ description, assay, dissolution, microbiological (where applicable), uniformity of content โ before the QA team issues a Batch Release Certificate.
Products are packed as per your approved artwork and dispatched with Certificate of Analysis (CoA), Certificate of Compliance (CoC), and Batch Manufacturing Records. We coordinate with your preferred freight partners for Pan-India delivery.
Fill in your requirements and our team will get back to you within 24 business hours.
Our business development team will review your enquiry and provide you with a detailed commercial proposal including pricing, lead times, and technical specifications.
Response within 24 business hours
Competitive price quote with no hidden charges
Technical feasibility confirmation from our QA team
Free sample product evaluation available
NDA signed before sharing any confidential information
Direct line: +91 88002 06259
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