V-Ensure Pharma Technologies
V-Ensure Pharma Technologies is a pharmaceutical company dedicated to scientific research, formulation development, analytical services, and manufacturing. They serve global markets with a focus on quality, innovation, and regulatory compliance. Their services include formulation R&D, API R&D, analytical services, and cGMP manufacturing, with a strong emphasis on pharmaceutical development and technology.
Industries
Nr. of Employees
small (1-50)
V-Ensure Pharma Technologies
Products
Injectable dosage form development
Development of injectable systems including emulsion-based delivery, nano-emulsions, particle-engineered long-acting suspensions, lyophilized formulations and dual-chamber prefilled systems.
Solid oral dosage forms
Development and manufacture of solid oral products including immediate-release tablets and capsules, modified-release tablets and capsules, pellets and mini-tabs, and sachet granules.
Liquid oral formulations
Development of liquid oral products including solutions, suspensions and powders for oral suspension.
API R&D
API research and development services providing bandwidth for niche and complex molecules including patent landscaping, polymorph screening, development of KSMs, intermediates, APIs, regulatory DMF filing, analytical development, and technology transfer.
cGMP Manufacturing Facility
Solid oral dose form manufacturing and contract manufacturing services provided by V-Ensure Pharma Technologies in a green field manufacturing facility.
Analytical Laboratory Services
A newly designed and constructed facility spread across 24,000 square feet, equipped to handle development, method validations, batch release, and stability studies.
Injectable dosage form development
Development of injectable systems including emulsion-based delivery, nano-emulsions, particle-engineered long-acting suspensions, lyophilized formulations and dual-chamber prefilled systems.
Solid oral dosage forms
Development and manufacture of solid oral products including immediate-release tablets and capsules, modified-release tablets and capsules, pellets and mini-tabs, and sachet granules.
Liquid oral formulations
Development of liquid oral products including solutions, suspensions and powders for oral suspension.
API R&D
API research and development services providing bandwidth for niche and complex molecules including patent landscaping, polymorph screening, development of KSMs, intermediates, APIs, regulatory DMF filing, analytical development, and technology transfer.
cGMP Manufacturing Facility
Solid oral dose form manufacturing and contract manufacturing services provided by V-Ensure Pharma Technologies in a green field manufacturing facility.
Analytical Laboratory Services
A newly designed and constructed facility spread across 24,000 square feet, equipped to handle development, method validations, batch release, and stability studies.
Services
End-to-end formulation development for solid oral, liquid oral and injectable dosage forms including QbD approaches, non-infringing formulation strategies, dossier preparation and regulatory filing support.
API and intermediate development including patent landscaping, polymorph screening, non-infringing synthetic route development, DMF filing support, analytical development and technology transfer.
Analytical method development, method transfer, method validation, stability study support and batch-release testing using chromatographic, spectroscopic and imaging techniques.
GMP-compliant contract manufacturing for solid oral finished dosage forms with integrated packaging; facility and production equipment for granulation, compaction, coating, capsule filling and packaging.
End-to-end formulation development for solid oral, liquid oral and injectable dosage forms including QbD approaches, non-infringing formulation strategies, dossier preparation and regulatory filing support.
API and intermediate development including patent landscaping, polymorph screening, non-infringing synthetic route development, DMF filing support, analytical development and technology transfer.
Analytical method development, method transfer, method validation, stability study support and batch-release testing using chromatographic, spectroscopic and imaging techniques.
GMP-compliant contract manufacturing for solid oral finished dosage forms with integrated packaging; facility and production equipment for granulation, compaction, coating, capsule filling and packaging.
Expertise Areas
- Formulation development for oral and parenteral dosage forms
- Controlled-release and multiparticulate systems
- API process development and intermediates
- cGMP commercial manufacturing for solid oral products
Key Technologies
- Hot-melt extrusion
- OROS and modified-release platforms
- Multi-unit particulate systems
- Nano-emulsion formulation
News & Updates
A fully operational facility capable of handling major solid oral dosage forms with advanced equipment, serving markets in USA, Europe, Canada, Australia, and others.
Recognized as a trusted contract research and development partner, offering end-to-end dossier development, formulation, and IP strategies, with successful product delivery.
The analytical laboratory earned successful inspection by the US FDA in February 2020, demonstrating quality and compliance.
A fully operational facility capable of handling major solid oral dosage forms with advanced equipment, serving markets in USA, Europe, Canada, Australia, and others.
Recognized as a trusted contract research and development partner, offering end-to-end dossier development, formulation, and IP strategies, with successful product delivery.
The analytical laboratory earned successful inspection by the US FDA in February 2020, demonstrating quality and compliance.