Medkyn Lifecare offers contract manufacturing and third-party / private-label manufacturing for both pharmaceutical formulations and nutraceutical supplements. Our facility in Naroda, Ahmedabad operates under WHO-GMP (World Health Organization Good Manufacturing Practice), FSSAI (Food Safety and Standards Authority of India), ISO 9001:2015, and GMP certifications, manufacturing tablets, capsules, soft gels, granules, sachets, and chewable tablets for brand owners across India.
A single Ahmedabad facility producing the full range of pharmaceutical and nutraceutical dosage forms — single point of accountability, consistent quality, faster time to shelf for your brand.
Compressed pharmaceutical and nutraceutical tablets, chewables, film-coated, sugar-coated. Multiple sizes, shapes, and embossing.
Hard-shell two-piece capsules — gelatin and vegetarian (HPMC). Powder, pellet, and granule fills.
Soft gelatin capsules for oil-soluble nutraceutical actives — Omega-3, Vitamin D3, Vitamin E, herbal oil extracts.
Single-dose stick-pack and pillow-pack sachets for granular nutraceuticals — amino acids, electrolytes, protein blends.
Pharmaceutical and nutraceutical syrups, suspensions, oral drops, eye/nasal drops in PET and amber glass.
Pharmaceutical ointments, creams, gels, and bulk/unit-dose powders. Tubes, jars, and bulk pack.
Share your formulation idea, dosage form, target market, and projected volumes. We respond with a feasibility note covering raw material availability, regulatory pathway (drug license vs. FSSAI), MOQ, and indicative pricing.
Our R&D team develops or refines the formulation. Lab-scale trials, taste/odour/disintegration profiling, stability protocol design, and ingredient sourcing finalised.
Pilot batch produced. You receive samples, full Certificate of Analysis, and stability initiation data. Sign-off on artwork, label, and pack.
Commercial-scale manufacturing under WHO-GMP, FSSAI, and ISO 9001:2015 quality systems. Batch records, in-process controls, and finished product release per agreed specifications.
Complete batch documentation — Certificate of Analysis, manufacturing/expiry batch records, GMP/FSSAI certificates as applicable. Dispatched to your warehouse or directly to distributors.
Every contract manufacturing batch ships with full pharmaceutical and nutraceutical regulatory documentation — ready for your QC review, distributor onboarding, or export filing.
Pharmaceutical formulations and nutraceutical supplements produced under one roof in Ahmedabad — single-source accountability and consistent compliance.
WHO-GMP, FSSAI, ISO 9001:2015, and GMP certifications. In-house QC laboratory with raw-material identity, in-process, and finished-product release testing.
Clear MOQ tiers and indicative pricing shared early. No hidden tooling, surprise tooling, or ambiguity on inclusions.
India-anchored sourcing wherever feasible. Stable supply chain governed by Indian pharmaceutical and food safety law (CDSCO, FSSAI).
MOQs depend on the dosage form and whether the formula already exists. Stock tablet and capsule formulas start at a few thousand units per SKU; custom formulations require a full production batch; soft gels carry higher minimums; and sachets are quoted in kilograms of blend. We share a written MOQ and pricing tier at the feasibility stage, before any commitment.
For an existing formula, typically 8–14 weeks: feasibility note, specification sign-off, artwork compliance review, raw material and packaging procurement, manufacturing, QC release and dispatch. A new custom formula that needs accelerated stability data before a shelf life can be assigned adds roughly 8–12 weeks.
Yes. Pharmaceutical formulations and nutraceutical supplements are produced under the same WHO-GMP certified, FSSAI-approved, ISO 9001:2015 quality system in Ahmedabad — one set of batch records, in-process controls and release testing for both categories.
A Certificate of Analysis covering physical, chemical and microbiological parameters, a manufacturing batch record extract, copies of our WHO-GMP and FSSAI certificates, allergen and vegetarian/non-vegetarian declarations, approved artwork files and, on request, stability data and a Free-Sale Certificate for exports.
Yes. Nutraceutical packs must carry both the manufacturer's and the marketer's FSSAI licence numbers, so you need an FSSAI licence for your company (Central licence for multi-state sales). Pharmaceutical products additionally require the appropriate drug licences for the marketer. We advise on the regulatory pathway in the feasibility note.
Both. Our R&D team develops or refines formulations — lab-scale trials, taste and disintegration profiling, stability protocol design and ingredient sourcing — and we also offer third-party manufacturing of existing Vitakyn-type formulas under your brand for a faster, lower-cost launch.
Read more before you brief us: how to start your own nutraceutical brand in India, what drives contract manufacturing costs, MOQs and timelines in India, third-party pharmaceutical manufacturing in Ahmedabad, and how to read a Certificate of Analysis.
Tell us your product idea, target dosage form, and projected volumes in the form above. Our team will respond within one business day with a feasibility note and indicative pricing.
Send a manufacturing briefOr call +91 94279 85519