Ayurvedic and Herbal Third-Party Manufacturing in Mohali, Punjab
Rehaan Healthcare works with businesses planning Ayurvedic and herbal product ranges from Sector 82, Mohali, Punjab. Share your product brief to discuss the intended formulation, dosage form, packaging and applicable requirements before a manufacturing plan is agreed.
A manufacturing conversation built around your product and market.
A third-party manufacturing project needs more than a product name. It needs an agreed dosage form, a defined formula or formulation brief, suitable packaging, clear claims and an understanding of the rules that apply to the product.
Rehaan Healthcare is based at Plot No 529 JLPL, Sector 82, Mohali, Punjab 160055. We invite pharma marketing companies, PCD businesses, wellness brands, clinics and new product teams to share their requirements for Ayurvedic and herbal products.
The first step is to establish what you want to make and where you intend to sell it. The applicable product category, licence scope, formulation, testing, minimum order and lead time must be confirmed for the specific project rather than assumed in advance.
Important: Manufacturing formats, licences, testing arrangements, order quantities and timelines are product- and facility-specific. Request current supporting documents before making a supplier decision.
Manufacturing support from brief to batch planning.
Start with the commercial requirement, then define the technical and compliance questions that must be answered before production is confirmed.
Product brief and formula review
Document the product concept, proposed ingredients, dosage form, target customer, market and intended claims.
Understand third-party manufacturing ↗Third-party manufacturing
Review how a licensed manufacturing arrangement works, which responsibilities belong to each party and what documents to request.
Read the manufacturing guide ↗Private-label planning
Bring your brand, packaging preferences and intended positioning into the project brief before costs and feasibility are finalized.
Private-label manufacturing ↗Product-format selection
Compare formats and define which options fit the product, label, intended use and manufacturing scope.
Explore product categories ↗Quality and documentation
Request relevant licence details, product specifications, test records and batch documentation for the product under review.
Quality documentation guide ↗Packaging and label review
Bring the pack format, artwork, marketer details and proposed claims into review before printing or production.
See the project process ↗Choose a format to begin the discussion.
The formats below are common in Ayurvedic and herbal product planning. Rehaan’s current manufacturing scope, licence coverage, specifications and availability must be confirmed for each format before a quotation is issued.
Tablets
For example, tablet or vati-style concepts where the formula, dose, pack and applicable category have been defined.
Ask about tablet manufacturing ↗Capsules
Discuss ingredient selection, capsule-shell requirements, serving instructions and packaging options.
Review product categories ↗Syrups and liquids
Define the product base, intended use, pack size, preservation needs and required testing before proceeding.
Understand the process ↗Powders and churna
Review ingredient identity, blend specifications, moisture controls and suitable pouches or jars.
Explore powder formats ↗Oils and topical formats
Discuss the proposed ingredients, product classification, packaging and whether the facility is licensed for the format.
Check format suitability ↗Other product concepts
Share your formulation or concept first. Feasibility depends on the product category and confirmed manufacturing capabilities.
Send your product brief ↗A defined path from initial brief to dispatch planning.
Each project should have a written scope, clear approvals and an agreed set of product documents. Actual steps and timings depend on the product and applicable permissions.
Share the brief
Provide product type, dosage form, proposed ingredients, target market, claims and estimated first order.
Review category and feasibility
Identify the regulatory route, licence scope, formulation questions and information still needed.
Agree specifications
Document the product specification, pack, tests, quantity assumptions and quotation basis.
Approve samples and artwork
Where sampling is available, review the sample and approve compliant packaging artwork before a commercial run.
Confirm batch and checks
Agree batch records, quality checks, release documents and responsibilities in writing.
Release and dispatch
Confirm the required release documents and dispatch arrangements for the approved order.
Ask for evidence that matches the product and facility.
A credible supplier evaluation starts with current documents, a clear product specification and a test plan appropriate to the formulation.
Quality assurance & documentation ↗- Manufacturing licence copy, issuing authority, validity and dosage forms covered.
- Applicable GMP or Schedule T documentation and its current scope.
- Product specification, ingredient details and raw-material documentation relevant to the formula.
- Finished-product test panel, certificate of analysis and laboratory arrangements.
- Stability evidence supporting the proposed shelf life and pack.
- Label and claims review under the rules applicable to the product category.
Do not treat a standard, certificate, test or licence as confirmed until the relevant document has been reviewed. The applicable framework differs between Ayurvedic medicines and food-category herbal products.
Build your own brand with a properly defined manufacturing brief.
Private-label planning brings the product concept, formula, pack design, marketer details and commercial requirements into one project. Responsibilities for formula ownership, approvals, packaging procurement and regulatory submissions should be written into the agreement.
- Product and target-market brief.
- Formula source, review and ownership terms.
- Packaging specification and label artwork.
- Quality documents, approvals and batch release requirements.
Prepare these details
- Company or brand name and business contact.
- Product category and proposed dosage form.
- Existing formula or ingredient brief, if available.
- Target market and intended claims.
- Packaging preference and expected first-order quantity.
- Any required test reports or documentation.
If some details are not final, submit the brief with what you know and list the open questions.
Common questions before choosing a manufacturer.
Start with the essentials, then review the detailed guides for manufacturing, product categories, quality and private label.
What is Ayurvedic third-party manufacturing?
It is an arrangement in which a licensed manufacturer produces an Ayurvedic medicine for a brand owner. The parties agree the product, formula, packaging, regulatory responsibilities and batch requirements before production.
Which formats can Rehaan manufacture?
Tablets, capsules, syrups, powders and oils are useful starting points for a product discussion. The actual formats available at Rehaan must be confirmed against the current manufacturing licence and facility capability.
What is the minimum order quantity?
Minimum order quantity depends on the product, dosage form, ingredients, packaging and batch economics. Request a written quotation that states the quantity and what is included.
How long does a first order take?
The timeline depends on formula readiness, ingredient sourcing, sample approval, label review, testing and the production schedule. Ask for a project-specific estimate after the specification is agreed.
How can I verify a manufacturer’s quality credentials?
Request current licence and applicable GMP documents, review their scope and validity, and ask for product-specific specifications, test records and batch documentation. Verify the documents with the issuing authority where possible.
Can I sell a product under my own brand?
Third-party and private-label arrangements can support a brand-owned product, subject to the product category, licence scope, label rules and written agreement between the parties.
Send the product brief. Define the next step.
Tell us what you want to make, where you intend to sell it and the quantity you have in mind. The team can then review the information needed to assess the project.