About Pharma Third Party Manufacturing & Job Works
Third Party Manufacturing & Job Works
We Providing Third Party Manufacturing/ Pharma Job Work
Our manufacturing unit is based at Village Madhopur, Saliyar - Madhopur Road, Roorkee (Uttarakhand). A pollution free, excise free zone where CST applicable is only 1% compared to 2% in other state.
The infrastructure, machines & environment are as per the revised schedule M (i. e eq. to. WHO-GMP std. ). with the state- of- the art facilities of mfg. by automatic machines for Tablets/Capsules/Liquids & Vet Boluses (for veterinary) and food and feed supplements.
The vast infrastructures have a covered area of 35000 sq. feet with complete control of air in & out and temp. Control through A. H. U. (Air Handling Unit) compiling all the statutory drug requirements and R & D norms.
All the machines, mostly automatic are of Stand Steel (S. S. ) made & fulfills the GMP norms & are being handled by efficient & experienced mfg. personnel's. Our manufacturing capacities:
Tab. section - 6. 00 lac's / day
Cap. section - 1. 50 lac's / day
Liq. section - 50000 Bottle / day
Vet. Bolus - 1. 00 lac's / day
Feed & Food supplements
ALU ALU Packs also available
We have enough spare capacities for third party mfg. / job work For interested parties
Versatile Manufacturing SolutionsOur contract and job work services are designed to cover a full spectrum of pharmaceutical requirements, including tablets, capsules, syrups, ointments, and injectables. Whatever the form, we offer manufacturing, packaging, and labeling tailored to client specifications, ensuring seamless operations and product diversity.
Certified Quality & Regulatory AssuranceWe maintain ISO and GMP certifications and strictly follow regulatory guidelines as per the Drug Regulatory Authority. Our processes are supported by thorough quality control measures, expert documentation, and regulatory compliance support, giving you peace of mind regarding product safety and efficacy.
Customizable and Efficient OperationsWhether you require small, medium, or large batch sizes, we provide flexibility without compromising timelines or quality. Clients can choose raw material sources and customize packaging (strip, bottle, blister, sachet), aligning with unique branding and market needs, ensuring both convenience and seamless distribution across India.
FAQs of Pharma Third Party Manufacturing & Job Works:
Q: How does Pharma Third Party Manufacturing & Job Works support custom product requirements?
A: We offer customization for formulation, packaging, and labeling as per specific client needs. Whether you require tablets, syrups, or injectables, our team collaborates closely to align with your exact specifications, including packaging options and batch sizes.
Q: What is the process for starting a contract manufacturing project with your company?
A: Simply contact us with your requirements. After discussing your product specifications and desired quantity (minimum 500 units), we handle documentation, regulatory compliance, material sourcing (from client or us), manufacturing, and delivery. Timelines are set as per order details.
Q: When can I expect product delivery, and how is timeliness ensured?
A: Delivery timelines depend on the order size and complexity but are always discussed upfront. We emphasize timely delivery through streamlined operations and coordinated logistics, so you can plan distribution with confidence.
Q: Where do you source raw materials for manufacturing?
A: Raw materials can either be provided by the client or sourced by us, depending on the clients preference. Both options undergo stringent quality checks to comply with industry standards and ensure final product excellence.
Q: What are the benefits of partnering with you for third party pharmaceutical manufacturing?
A: Clients benefit from access to certified manufacturing facilities, batch size flexibility, regulatory support, comprehensive quality assurance, and personalized customer service, all supporting robust and efficient product launches across India.
Q: How does your company ensure compliance with Indian drug regulations?
A: We strictly adhere to guidelines set by the Drug Regulatory Authority, ensure all necessary documentation, and maintain updated certifications (ISO, GMP). Our regulatory support team manages filings and compliance, minimizing risks and delays.