Inova Pharma & Life Science
We are agile and flexible Contract Development Organization that serves pharmaceutical and biotechnology companies across the globe.

Innovation with Passion

Committed to providing highest quality services with high levels of client satisfaction

Inova Pharma and Life Sciences laboratories is over five years of global experience in specialized pharmaceutical and medical development testing and analysis. Inova is a distinctive company, with customer relationship skills that set us at very high standards. Integrity, reliability, confidentiality, and cost-effectiveness are the main cornerstones of all our services.
What we are passionate about

Innovation and Value Added Medicines (Super-Generics)

  • We are specialised in the development and registeration of value-added medicines and drug combination (super-generics). Also, in the development of products for 505B2 submission.
  • Therapeutic areas:
    ● Cardiovascular system   ● Gastroenterology    
    ● Pain management and Rheumatology
    ● Antibiotics & Infectious Diseases   ● Urinary system
    ● Diabetic molecules & Endocrine  ● ENT & Respiratory
    ● Neuroscience Research  ● Oncology Ophthalmology
    ● Paediatrics medicines  ● Biotechnology development
    ● Nephrology and Renal Diseases

Our Solutions

Whether you require drug substance process route selection, bioanalysis, synthesis, scale up of APIs/HPAPIs or final drug product manufacture, we have the expertise to deliver quality solutions.
Formulation & Process Development
Analytical Services
Quality System Support
Scale-up Troubleshooting
CMO Services
Out/In Licensing
Innovative Solutions

Formulation & Process Development

  • Oral Drug Development
  • Soft Gel Capsules
  • Hard Gelatine Capsules
  • Sterile & Parenteral Drug Development
  • Aseptic Development
  • Dosage Forms Preformulation Studies
  • Large Molecule Biologics Development
  • Spray Drying
  • Lyophilization
  • Highly Potent Development
  • Vaccine Fill-Finish Technology
  • Small Molecule Development
  • Oral Solid Dose
Data you can rely on
with uncompromized integrity

Analytical Stability Studies

Inova performs all stability studies in support of all stages of formulation development
  • Early Development Stability
  • Excipient Compatibility
  • Component Compatibility
  • Solubility Studies
  • Photostability Studies
  • Photostability Studies
  • Thermal Cycling and Freeze-thaw Studies

Analytical Services
& Testing Capabilities

Our laboratories complies with strict cGMP/GLP requirements. Quality system is based on comprehensive SOPs and rigorous quality assurance practices.

At Inova we apply QbD Principles to Analytical Development. We have extensive experience in method development and validation with a profound understanding of all aspects of the drug-development process.
  • HPLC / UPLC testing with a wide variety of detection capabilities
    (UV, DAD, RI, CAD, ECD)
  • Dissolution Testing (USP Apparatus I, II, III &IV)
  • GC / Headspace analysis
  • UV/VIS spectrophotometry
  • FTIR spectroscopy
  • Cleaning Method Development, Verification, and Validation
  • Wet Chemistry Analysis
  • Microbial Analysis
  • USP testing
  • Sterility and Bacterial Endotoxin testing
  • Container Closure Integrity Testing (CCIT)
  • Solid State Chemistry Process Development
  • Full analytical method Validation
  • Technology Transfer & Scale-up manufacturing
    Full support in all phases until commercialization and manufacturing tweak-ups. Also, we support our customers with analytical method transfers.
  • Pipeline development & optimization
    We collaborate with our customers to develop their portfolio selection or doing optimization according to latest market analysis.
  • Turnkey solutions for new
    manufacturing sites
    Inova dedicated team to design build and offer turn key solution to new manufacturing site and green field solutionInova can install and qualify new production lines with all required tests to meet GMP requirements.
  • Clinical studies
    and Bioequivalence support
    Biostudies monitoring. Comparative dissolution profiling and Invitro studies. Biostudies evaluation

Helping our customers navigate their way to success

  • Quality Assurance: System audit upgrade and support. Building Quality system according to EU-GMP requirements.
  • Regulatory Support and dossier compilation. Support in regulatory authorities’ questions.
  • Common technical documents (CTD) preparation and amendment.
  • Life cycle management for approved applications with regulatory assessment of post-approval changes, strategy and supplements
Position your product

Marketing & Knowledge Area

We have a strategic partnership with Konsipta to provide our customers creative marketing and designing solutions to support their projects.
  • Branding Strategy
  • Packaging Design
  • Medical Copywriting
  • Medical Brochures
  • Digital & Web-Development
More information

Get in touch.

46 Powerstown Way
Clonmel, County Tipperary
E91H583, Ireland
info@inova.ie

46 Powerstown Way
Clonmel, County Tipperary
E91H583, Ireland
info@inova.ie

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