Manufacturing · WHO-GMP · ISO 9001:2015 · FSSAI · HACCP · AYUSH
WHO-GMP Certified Manufacturing Across Pharmaceutical, Nutraceutical & Herbal Divisions
Biofril Healthcare’s Nalagarh manufacturing facility produces across the full pharmaceutical dosage spectrum — sterile parenteral preparations, solid oral dosage forms, liquid orals, softgel capsules, powders, gummies, and ayurvedic preparations. Single regulatory-compliant facility. Complete multi-division compliance. PCD franchise partners and contract manufacturing clients welcome.
Manufacturing Capabilities
Comprehensive Production Across All Four Divisions
- Critical Care Parenteral Preparations: Sterile production lines for vials, ampoules, lyophilised injections, and infusion bags. 273+ formulations spanning anti-infectives, antimalarials, neurology, pain and inflammation, gastrointestinal, hormones, and infusions.
- General Pharmaceutical Manufacturing: Solid dosage lines for tablets (uncoated, film-coated, sugar-coated, enteric-coated) and capsules. Liquid oral preparation lines for syrups, suspensions, and oral drops. 200+ formulations.
- Nutraceutical Manufacturing: Hard gelatin capsules, vegetarian (HPMC) capsules, softgel capsules, tablets, powders, protein powders, effervescent tablets, and confectionery dosage forms (gummies). 95+ formulations under FSSAI Central License. Detailed nutraceutical contract manufacturing →
- Herbal & Ayurvedic Manufacturing: AYUSH-licensed production of classical and patent ayurvedic preparations including tablets, capsules, syrups, churnas, medicated oils, and lehyams.
Quality Assurance Programme
In-House Quality Control at Every Production Stage
- Raw material qualification: High-Performance Liquid Chromatography (HPLC) and Fourier-Transform Infrared (FTIR) spectroscopy for identity verification, assay quantification, microbial limit testing, and heavy metal analysis
- In-process quality controls: Weight variation, hardness, friability, and disintegration testing at 30-minute intervals across production runs
- Finished product release testing: Dissolution, assay, microbial enumeration, and stability-indicating parameters prior to Quality Assurance release authorisation
- Certificate of Analysis (COA) issued with every batch dispatch
- Stability monitoring programme: 25°C/60% RH, 30°C/65% RH, and 40°C/75% RH chambers tracking 24- to 36-month shelf-life data per ICH Q1A(R2) guidelines
- Documentation infrastructure: Batch Manufacturing Records (BMR), Batch Packaging Records (BPR), deviation reports, change control records, and Corrective and Preventive Action (CAPA) documentation maintained for regulatory inspection traceability
Regulatory Compliance Standing
Certifications Across All Manufacturing Divisions
- WHO-GMP certification for pharmaceutical and parenteral preparation manufacturing
- ISO 9001:2015 Quality Management System certification
- FSSAI Central License for nutraceutical, health supplement, and food-related production
- HACCP certification for food safety compliance
- AYUSH Manufacturing License for ayurvedic and herbal pharmaceutical production
- Cleanroom classifications from Grade A through Grade D as per product-specific requirements (per ISO 14644-1 standards)
Engagement Models
PCD Distribution or Contract Manufacturing
- PCD Franchise: Distribute Biofril-branded products in a designated monopoly territory. Explore PCD Franchise →
- Contract Manufacturing / Private Label: Launch a proprietary brand with production undertaken under client labelling. Available across nutraceutical, herbal, and general pharmaceutical formulations. Minimum Order Quantity (MOQ) commencing at 5,000 units per Stock Keeping Unit (SKU).
Request a Manufacturing Proposal
Communicate your target division, intended formulation, projected volume, and required delivery timeline. Our business development team will respond within 24 to 48 business hours.