Bioequivalence & Bioavailability Services & Phase I-IIa

Bio-innovaBioequivalence & Bioavailability Services

Our comprehensive services
embrace protocol development to
final study reports and are in
compliance with ICH-GCP, ISO/
IEC17025 and GLP requirements.
  • Protocol development
  • Regulatory approval
  • Ethics Committee approval
  • Study population
  • Clinical study
  • Analytical method development
    and validation
  • Bioanalysis
  • Data management and statistics
  • Report writing and submission
  • Quality assurance

Frequently Asked Questions

He has developed essays in the following areas: UPLC-MS/MS, GC-FID, in vivo microdialysis, HPLC-(UV, fluorescence, electrochemical).
What products are cosmetics?

Podcasting operational change management inside of workflows to establish a framework. Taking seamless key performance indicators offline to maximise the long tail.

Is animal testing required?

Collaboratively administrate empowered markets via plug-and-play networks. Dynamically procrastinate B2C users after installed base benefits.

What are the alternatives?

Dramatically visualize customer directed convergence without revolutionary ROI.

Where is animal testing safe?

Keeping your eye on the ball while performing a deep dive on the start-up mentality to derive convergence on cross-platform integration.

Our Expertise

Improve products to make them safer
and more accessible

Accurate Product Testing by Expert Scientists

Opening hours


10am - 5pm


10am - 5pm


10am - 6pm


10am - 6pm


10am - 6pm

Sat - Sun


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