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Research & Development (R&D)

At Vital Therapeutics & Formulations, our Research & Development Centre is built to push the boundaries of formulation science. With next-generation nano-technology platforms, advanced dosage design, and a multidisciplinary scientific team, we specialize in transforming complex actives into stable, bioavailable, patient-centric formulations for both pharmaceutical and veterinary use. 

Our R&D ecosystem integrates Formulation DevelopmentAnalytical Research, and Innovation Engineering, enabling fast, reliable, and commercially scalable solutions for global markets. 

Formulation Research & Development (FRD)

Vital’s Formulation Research & Development (FRD) team transforms complex actives into stable, high-performance, and patient-centric dosage forms across pharmaceuticals, veterinary health, and nutrition. With deep expertise in nano-systems, solubility enhancement, taste-masking, and delivery optimisation, we design formulations that deliver superior bioavailability and therapeutic impact. Every product is engineered for manufacturing, regulatory compliance, and commercial feasibility from day one.

Capabilities: 

  • Oral liquids and suspensions
  • Pediatric drops & palatable suspensions for bitter actives
  • Nano suspensions & nano liquid formulations
  • Solid emulsions (SNEDDS), micro emulsions, multiple emulsions
  • Nano emulsions
  • Insta-sol powders, effervescent powders, bulk powders
  • Dry syrups & pellets
  • Tailor-made formulations for improved palatability, stability, and patient acceptability
  • Solubility & permeability enhancement
  • Taste masking technology
  • Bio-nano functional excipients for actives, vitamins, minerals, amino acids & enzymes

OUR EXPERTISE

RESEARCH & DEVELOPMENT

In-house R&D units driving innovation across multiple dosage forms.

NEW FORMULATION DEVELOPMENT

Rapid prototyping, analytical development, and scalable technology transfer.

SCALE-UP & COMMERCIAL MANUFACTURING

Flexible batch sizes for clinical trials and full-scale production.

REGULATORY SUPPORT

Dossier preparation, stability studies, and assistance with product registration in Indian and global markets.

Advanced Drug Delivery Systems

Vital’s Advanced Drug Delivery Systems platform focuses on transforming therapeutic outcomes through cutting-edge nano-engineering and precision delivery technologies. By enhancing solubility, permeability, and targeted absorption, we enable lower dosages with higher efficacy across both pharmaceutical and veterinary applications. Our next-generation delivery systems are engineered to unlock the full potential of challenging APIs while improving patient compliance and treatment value.

Capabilities: 

  • Bio-nano formulations for pharmaceuticals & veterinary health
  • Novel Drug Delivery Systems (NDDS)
  • Dose minimization strategies
  • Nano-enabled solubility enhancement
  • Bio-nano excipient engineering
  • Lipid-based nano-systems
  • Specialized smart nanotechnologies for improved therapeutic efficiency
  • Nano liquids & nano suspensions
  • High-performance delivery for poorly soluble APIs

Commercialization & Scale Up

Our Commercialisation and Scale-Up division bridges innovation and industry with seamless technology transfer, pilot-scale optimisation, and robust process engineering. We ensure that every formulation developed at Vital transitions smoothly into large-scale manufacturing without compromising quality, stability, or performance. With disciplined validation practices and facility readiness, we accelerate your journey from laboratory concept to market-ready product.

Capabilities: 

  • Exploration of novel concepts for commercial application
  • Development of ultra–cost-effective veterinary & human pharma formulation solutions
  • Diversified product development for multi-segment markets

Analytical Development & Research

Vital’s Analytical Development and Research unit provides the scientific rigour required to support advanced formulation design and regulatory compliance. From method development and validation to impurity profiling, stability studies, and mass/NMR-based structural analysis, our team ensures accuracy, reproducibility, and global pharma-grade standards. Every analytical insight strengthens the safety, efficacy, and quality foundation of the products we develop

Capabilities: 

  • Method development
  • Method validation (Assay/RS/GC)
  • Stability studies (ACC & LT as per Zone IV-B)
  • Method transfer & method equivalence
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