Global Nutraceutical CDMO & Export Manufacturer

End-to-end formulation, GMP manufacturing, compliance, and international export support for nutraceutical products across regulated and emerging markets.

MANUFACTURING DELIVERY FORMATS - CDMO 02
how we can help

We’ll ensure that you focus on the opportunities

End-to-end programs.

Lorem ipsum dolor sit amet, consectetur adipisicing elit, sed do eiusmod tempor incididunt ut labore et dolore magna aliqua. Ut enim ad minim veniam, quis nostrud exercitation ullamco laboris nisi ut aliquip ex ea commodo consequat.

Support Functions

Lorem ipsum dolor sit amet, consectetur adipiscing elit. Ut elit tellus, luctus nec ullamcorper mattis.

Service Operations

Lorem ipsum dolor sit amet, consectetur adipiscing elit. Ut elit tellus, luctus nec ullamcorper mattis.

Supply Chain

Lorem ipsum dolor sit amet, consectetur adipiscing elit. Ut elit tellus, luctus nec ullamcorper mattis.

WHO WE ARE

Bliss Life Sciences LLP is an India-based Global Nutraceutical Contract Development and Manufacturing Organization (CDMO) supporting domestic and international brands with formulation development, scalable production, regulatory compliance, packaging, and export-ready supply.

Our manufacturing ecosystem is designed to meet global quality benchmarks while supporting flexible volumes and long-term international partnerships.

Key Capabilities:

  • 200+ Active Global Brand Partnerships
  • 900+ Nutraceutical Formulations Developed
  • 12+ Dosage & Delivery Formats
  • Multi-Country Export Experience

OPERATIONAL CHALLENGES WE ADDRESS

  • Complex export regulations and documentation requirements
  • Market-specific ingredient and labeling restrictions
  • Inconsistent product quality across batches
  • Difficulty scaling from pilot to commercial volumes
  • Limited in-house regulatory and export expertise
  • Supply chain reliability for international markets

OUR GLOBAL CDMO SERVICES

Formulation & Product Development

  • Custom nutraceutical formulations
  • Vitamin, mineral, herbal & functional blends
  • Bioavailability and stability optimization
  • Pilot batches and validation runs
  • Market-specific formulation customization

Manufacturing & Quality Systems

  • GMP-certified manufacturing facilities
  • Pilot and commercial-scale production
  • In-process and final quality control
  • Batch traceability and validation
  • Certificates of Analysis (COA)

Regulatory & Export Support

  • FSSAI-compliant manufacturing
  • Export documentation systems
  • Stability and shelf-life studies
  • Country-specific labeling support
  • Packaging and logistics coordination
Numbers

Client results

Completed operations programs
0 +
Realized return on fees
0 x

GLOBAL EXPORT & MARKET READINESS

Our nutraceutical manufacturing systems are designed to support brands entering and scaling across international markets with varying regulatory and quality requirements.

Key export-focused capabilities include:

  • Market-adaptive formulations aligned with international regulations
  • Export-compliant raw material sourcing and specifications
  • Stability, shelf-life, and storage condition validation
  • Global-standard nutritional panels and labeling formats
  • Documentation support for commercial and institutional exports
  • Packaging compatibility for long-distance logistics and storage

Each product is developed to meet the expectations of regulated, semi-regulated, and emerging nutraceutical markets while maintaining quality consistency and compliance throughout the supply chain.

World Map

BRAND SEGMENTS WE SUPPORT

  • Startups & D2C Nutrition Brands
  • Growing Wellness & Supplement Companies
  • International Nutrition Corporations
  • Institutional & Corporate Wellness Programs

Our systems support both pilot launches and long-term high-volume supply.

QUALITY CERTIFICATES

Learn more

FAQs – Global Nutraceutical CDMO & Export Manufacturing

A Global Nutraceutical Contract Development and Manufacturing Organization (CDMO) provides end-to-end services including formulation development, GMP manufacturing, quality control, regulatory support, and export-ready supply for international nutrition brands.

Yes. We offer private label manufacturing (including formulation development) as well as contract manufacturing for client-owned formulations.

We manufacture products across wellness, preventive healthcare, sports nutrition, beauty nutrition, medical nutrition, and condition-specific health segments.

Yes. Formulations are customized based on target market regulations, ingredient restrictions, dosage limits, and consumer preferences.

Yes. We specialize in single-ingredient products as well as complex blends combining vitamins, minerals, herbal extracts, amino acids, and functional nutraceutical ingredients.

Yes. Pilot batches are available to validate formulation performance, stability, and market readiness before scale-up.

We support tablets, capsules, softgels, vegetarian softgels, powders, sachets, gummies, syrups, liquid formulations, protein powders, and functional nutrition blends.

Yes. All manufacturing operations follow GMP-compliant systems with validated processes and documented quality controls.

Consistency is maintained through standardized SOPs, qualified raw material sourcing, in-process quality checks, validated equipment, and full batch traceability.

Finished products are tested for:
• Assay and potency
• Microbial limits
• Heavy metals
• Stability and shelf life
• Physical and sensory parameters (where applicable)

Yes. All products undergo testing for common adulterants, contaminants, and regulatory-mandated safety parameters.

Yes. NABL-accredited third-party laboratory testing can be arranged upon request.

Yes. Products are manufactured under export-compliant quality systems with full documentation support.

We support:
• Certificate of Analysis (COA)
• Stability and shelf-life data
• Free Sale Certificate
• Product specifications
• Export-compliant labeling support

Yes. We assist with nutritional panels, ingredient declarations, claims alignment, and mandatory labeling formats as per target market requirements.

We support jars, bottles, blister packs, sachets, pouches, bulk packs, and export-grade secondary packaging.

Yes. Packaging compatibility, stability, and shelf-life are validated to withstand long-distance logistics and varied storage conditions.

Yes. We offer flexible MOQs, pilot runs, and regulatory guidance suitable for startups, D2C brands, and market testing.

Yes. Our infrastructure supports scalable production from pilot batches to high-volume commercial supply.

Yes. We follow strict confidentiality, data protection, and IP security protocols for all client projects.

Typical timelines:
• Formulation development: 2–4 weeks
• Pilot validation: 2–3 weeks
• Commercial manufacturing: 4–6 weeks
(Timelines vary based on product complexity and approvals.)

Yes. Our CDMO model is designed for long-term, scalable partnerships with global nutrition brands.

Ready to Launch?

Trusted by 200+ Brands