WHO-GMP CERTIFIED FACILITY • MOHALI, PUNJAB
Outsource your nutraceutical production to an audit-ready, WHO-GMP certified facility in Mohali, Punjab. Bionial Lifesciences delivers complete batch documentation, pharmacopoeial testing, and Certificate of Analysis with every single order — across 7 dosage forms and 218+ validated formulations. Your brand, our infrastructure, zero compromises on quality.
UNDERSTANDING THE MODEL
Third-party manufacturing is a production model in which an established brand outsources the entire manufacturing lifecycle — formulation, raw material sourcing, blending, compression or encapsulation, quality control testing, packaging, and regulatory documentation — to a licensed, GMP-certified facility. Unlike contract manufacturing, where brands may provide their own formulas, third-party manufacturing typically involves selecting from the manufacturer's existing library of validated formulations. This model allows pharma companies, FMCG brands, and nutraceutical distributors to expand their product catalogues rapidly without investing in dedicated production infrastructure. The brand retains full ownership of marketing, distribution, and sales, while the manufacturer handles every aspect of production, quality assurance, and compliance. For brands entering India's rapidly growing nutraceutical sector, third-party manufacturing eliminates the two largest barriers to market entry: capital expenditure on facilities and the timeline required to obtain manufacturing licenses.
WHY THIRD-PARTY MANUFACTURING
Eliminate the complexity of building your own manufacturing unit. Partner with an audit-ready facility and focus on growing your brand.
Setting up a WHO-GMP nutraceutical manufacturing facility requires an investment of several crores in land, equipment, clean rooms, QC labs, and licensing. Third-party manufacturing eliminates this entirely. You access Bionial's fully equipped facility in Mohali — including automated capsule-filling lines, tablet compression machines, syrup manufacturing vessels, softgel encapsulation equipment, and NABL-grade testing laboratory — without a single rupee of capital expenditure. Your investment goes into branding, marketing, and distribution instead of bricks and machinery.
Every batch manufactured at Bionial ships with a complete audit-ready documentation package that meets the standards expected by regulatory authorities, marketplace quality teams, and institutional buyers. This includes Batch Manufacturing Records (BMR), Batch Packaging Records (BPR), Certificate of Analysis (CoA) with identity, potency, heavy metals, microbial limits, and dissolution data, stability reports (both accelerated and real-time), and FSSAI-compliant labels. When your distributors, retailers, or marketplace platforms request compliance documentation, you have it ready — no scrambling, no gaps.
Whether you need 1,000 units for a test launch or 5,00,000 units for a nationwide rollout, Bionial's modular production lines scale with your demand. Our facility operates multiple parallel production streams across 7 dosage forms — capsules, tablets, softgels, syrups, powders, sachets, and Ayurvedic formulations — allowing us to handle volume surges without compromising quality or timelines. As your brand grows, your manufacturing capacity grows with it. No equipment purchases, no hiring production staff, no facility expansion headaches.
WHO IS THIS FOR
Three types of businesses drive the majority of India's third-party nutraceutical production demand.
Pharmaceutical companies with established distribution networks but no nutraceutical manufacturing license use third-party manufacturing to enter the wellness market. Bionial provides pharma-grade quality protocols, complete batch documentation, and regulatory support that meet the stringent internal standards pharma companies require. Our WHO-GMP certification and documentation practices align with the audit expectations of pharmaceutical quality assurance teams, making the transition from pharma to nutra seamless.
Fast-moving consumer goods companies are increasingly adding wellness supplements, herbal products, and functional health foods to their existing portfolios. Third-party manufacturing allows FMCG companies to leverage Bionial's 218+ validated formulations and launch new SKUs without diverting resources from their core business. From multivitamin gummies to Ayurvedic immunity boosters, FMCG brands can test multiple product categories and iterate quickly based on market response.
Brands that already manufacture in-house but face capacity constraints during peak seasons or product launches use Bionial as an overflow manufacturing partner. Our facility provides additional production capacity without the lead time of expanding your own operations. This is particularly valuable during festive seasons, marketplace sale events, or when launching multiple new SKUs simultaneously. All overflow production maintains the same quality standards and documentation as your in-house output.
COMPREHENSIVE OUTPUT
Every third-party manufacturing order from Bionial includes a complete production and compliance package. Nothing is an add-on — these are standard deliverables.
Batch Manufacturing Record (BMR) and Batch Packaging Record (BPR) for every production run, including in-process control data, equipment logs, environmental monitoring records, and personnel details. These documents provide full traceability from raw material receipt to finished product release.
Every batch ships with a detailed CoA covering identity testing, potency assay, heavy metal analysis (lead, arsenic, mercury, cadmium), microbial limits (TPC, yeast, mould, E. coli, Salmonella), dissolution and disintegration data, and moisture content. Results are benchmarked against pharmacopoeial specifications.
All analytical testing follows Indian Pharmacopoeia (IP), United States Pharmacopeia (USP), and British Pharmacopoeia (BP) methods as applicable. Our QC laboratory uses calibrated HPLC, UV-Vis spectrophotometry, dissolution apparatus, and microbiological testing equipment to ensure every parameter meets or exceeds specification.
We provide accelerated stability data (40°C/75% RH for 6 months) and initiate real-time stability studies (25°C/60% RH for 24 months) for every new formulation. This data supports your FSSAI shelf-life declarations and provides confidence to retailers and marketplace quality teams reviewing your product documentation.
Bionial's regulatory team assists with FSSAI product approval documentation, label compliance review, category classification, and claim substantiation. We ensure your products meet all mandatory labeling requirements including nutritional information panels, allergen declarations, vegetarian/non-vegetarian markings, and batch coding — so your products are marketplace-ready from Day 1.
Every engagement begins with a mutual Non-Disclosure Agreement (NDA). Custom formulations developed for your brand remain your intellectual property. Our facility uses segregated production protocols, access-controlled formulation records, and batch-specific documentation to ensure complete confidentiality of your product specifications and ingredient ratios.
MANUFACTURING CAPABILITIES
Every dosage form manufactured in our WHO-GMP facility with dedicated production lines, quality protocols, and packaging capabilities.
Hard gelatin and HPMC vegetarian capsules. Automated filling lines with weight variation control.
Oil-based and lipid formulations in seamless gelatin softgel capsules. Ideal for fat-soluble nutrients.
Coated and uncoated tablets with hardness, friability, and dissolution control on every batch.
Liquid orals in sugar-based and sugar-free formulations. Viscosity and pH controlled manufacturing.
Protein blends, green superfood mixes, and single-ingredient powders. Blending with particle-size uniformity.
Single-serve sachets for effervescents, ORS, protein powders, and granulated formulations.
Classical and proprietary Ayurvedic formulations under AYUSH GMP certification. Full herb testing and traceability.
Proprietary liposomal encapsulation for up to 29x bioavailability. Vitamin C, Iron, Glutathione, CoQ10.
CERTIFICATIONS & COMPLIANCE
Our facility holds three independent manufacturing certifications, each verified by authorized regulatory bodies.
Our facility is certified under World Health Organization Good Manufacturing Practice guidelines. This certification covers facility design, equipment qualification, process validation, personnel training, documentation systems, and quality management. WHO-GMP is the international gold standard for pharmaceutical and nutraceutical manufacturing quality, and our certification is verified through annual inspections and audits.
Bionial holds a valid FSSAI (Food Safety and Standards Authority of India) manufacturing license. This license is mandatory for all food and supplement manufacturers in India and covers our production, packaging, labeling, and storage operations. Our regulatory team ensures every product we manufacture meets current FSSAI labeling requirements, nutritional claim regulations, and food safety standards.
For Ayurvedic and herbal formulations, our facility holds AYUSH GMP certification issued under the Drugs and Cosmetics Act. This certification specifically covers Ayurvedic, Unani, Siddha, and Homeopathic manufacturing and requires compliance with Schedule T GMP standards including raw herb identity testing, heavy metal limits, aflatoxin screening, and microbial quality parameters specific to botanical products.
FREQUENTLY ASKED QUESTIONS
Answers to the most common questions from brands evaluating third-party nutraceutical manufacturing partners.
Every order ships with a complete documentation package: Batch Manufacturing Record (BMR), Batch Packaging Record (BPR), Certificate of Analysis (CoA) covering identity, potency, heavy metals, microbial limits, and dissolution, stability data (accelerated and real-time), FSSAI-compliant product labels, and a regulatory compliance dossier. This documentation package ensures your products are audit-ready from the first batch — whether you are selling through retail, e-commerce, or institutional channels.
Yes. Our WHO-GMP certified facility in Mohali is designed for scalable production. We manufacture across 7 dosage forms — capsules, tablets, softgels, syrups, powders, sachets, and Ayurvedic formulations — with capacity to handle orders from 1,000 units per SKU up to multi-lakh bulk production runs. Our modular production lines allow simultaneous manufacturing of multiple SKUs without cross-contamination risk, making us suitable for both test batches and large-volume commercial orders.
Bionial offers category-level and formulation-level exclusivity arrangements on a case-by-case basis. For brands requiring that a specific formulation or ingredient combination is not manufactured for competing brands, we execute a formal exclusivity agreement with defined terms, territory, and duration. This protects your competitive advantage while giving you access to our manufacturing infrastructure. Contact our business development team to discuss exclusivity options for your product line.
We welcome facility audits and encourage them as part of due diligence. The process is straightforward: schedule a visit through our business team, and we provide a guided walkthrough of our entire production facility — raw material warehouse, blending area, compression and encapsulation zone, coating section, QC laboratory, packaging lines, and finished goods storage. All areas are maintained to WHO-GMP standards with controlled access, environmental monitoring, and real-time cleaning validation. We also share our GMP certificate, FSSAI license, AYUSH GMP certificate, and recent third-party audit reports upon request.
IP protection is foundational to our third-party manufacturing model. Every engagement begins with a mutual Non-Disclosure Agreement (NDA). Custom formulations developed for your brand are your intellectual property — we do not replicate, share, or sell them to other clients. Our facility uses segregated production protocols, access-controlled formulation records, and batch-specific documentation to ensure complete confidentiality of your product specifications, ingredient ratios, and manufacturing parameters. For brands with specific IP concerns, we offer additional contractual safeguards.
Tell us about your product requirements. Our team will respond within 24 hours with a detailed proposal, pricing, timeline, and sample availability — no obligation, no minimum commitment to get started.