Complex questions about bioactive ingredients?

Before we talk about methods, we want to understand your project. We analyze it together in a structured assessment:

YOUR CURRENT
SITUATION

  • What regulatory 
    requirements apply?
  • What evidence is 
    already available?
  • What are the critical 
    success factors?

YOUR GOALS

  • Health claim 
    substantiation?
  • Novel food approval?
  • Product differentiation?
  • Quality standardization?

YOUR ROADMAP

  • Which steps are required?
  • In which order?
  • With what 
    budget and schedule?

DOES THIS SOUND FAMILIAR?

TYPICAL PROBLEM SCENARIOS

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RAW MATERIAL QUALITY ASSURANCE

"Our botanicals show variable quality between batches."

COMMON PITFALLS:

  • Natural fluctuations
  • Lack of bioactivity markers
  • Insufficient specifications
  • Batch-to-batch variability

OUR APPROACH:

Analytics + Bioassays → Standardization → Batch control

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HEALTH CLAIM SUBSTANTIATION

"We need scientific evidence for our health claims."

COMMON PITFALLS:

  • Unclear EFSA requirements
  • Incorrect study endpoints
  • Insufficient characterization
  • High costs for clinical studies


OUR APPROACH:

Claim strategy → Fit-for-purpose study design → Rationale/dossier

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PROVE MARKETING CLAIMS

"We want to back up our product promises scientifically."

COMMON PITFALLS:

  • Unclear legal boundaries
  • Lack of scientific evidence
  • Uncertain market positioning
  • Unclear competitive differentiation


OUR APPROACH:

Claim strategy → Appropriate studies (in vitro/clinical) → Reliable marketing claims

OUR SEAMLESSLY INTEGRATED APPROACH

FROM ANALYSIS TO SOLUTION

As a full-service partner, we coordinate all the necessary services – but only those that your project really needs. No over-engineering, no unnecessary costs. Instead: An interdisciplinary team that understands your challenge holistically and develops the optimum solution.

1. STRATEGIC ASSESSMENT

2. CUSTOMIZED ROADMAP

3. INTEGRATED IMPLEMENTATION

  • Building blocks from the three departments
  • Always: Regulatory Affairs / regulatory classification

4. MARKET SUCCESS

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Three
core
advantages

ONE CONTACT – for all project phases

ONE INTEGRATED TEAM – analysts, biologists, nutritionists and regulatory experts work hand in hand

A CLEAR ROADMAP – transparent and budgetable right from the start

 

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SERVICE AREAS

OUR SOLUTION MODULES – INDIVIDUALLY COMBINED

Depending on your challenge, we combine the appropriate services from three core areas:

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ANALYTICS

WHEN YOU NEED IT:

  • Raw material characterization
  • Quality control
  • Stability tests
  • Identity testing

We provide precise analytical data as a basis for scientific statements and regulatory requirements.
 

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In vitro test systems

WHEN YOU NEED IT:

  • Proof of concept
  • Mechanistic studies
  • Safety tests
  • Batch-to-batch control

We investigate biological effects in controlled systems – cost-effectively and with regulatory relevance.

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Nutritional CRO

WHEN YOU NEED IT: 

  • Health Claim Substantiation
  • Human intervention studies
  • Bioavailability studies
  • PMCF studies

We plan and implement clinical studies according to the highest scientific standards – fit-for-purpose and budget-optimized.

Find out more
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LET US
ANALYZE
YOUR
CHALLENGE

In a free initial consultation, we structure your project together and show you possible solutions – without obligation and based on our 25 years of experience.

 

Contact us

WOULD YOU LIKE TO KNOW
WHAT
WE KNOW?

We regularly publish scientific articles.

Do you have a complex question?

We’re happy to provide you with personalized, expert advice.

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