GENERATING TRUST

Bringing your product into the regulatory spotlight of your own accord, speaks trust. During product launch, it is often considered advisable to declare a formal petition with the government. Doing so is an instant validation of the standard, quality and efficacy of your product

In the US market, a Citizen Petition is often raised with the Food and Drug Administration (FDA). The petition could either request action or request restraint from taking action.

Bringing your product under regulatory focus, works for strategic marketing as it directly increases consumer confidence, and subsequently, increases profitability.

But, submitting a citizen petition is a complex task. However, TulipLab’s team of expertize works at providing the best personalized solution to meet the regulatory needs of your country as well as international mandates.

Our team supports the following:

• Expert toxicologists provide insider perspective on efficacy and quality of an ingredient or product.
• Technical reviews help claim substantiation.
  
• GAP analysis ensures all claims meet FDA requirements. It also identifies all applicable regulatory requirements as well as risks. This helps us create customized solutions for your ingredient or product.
  
• Data analysis supports data requirements for protocol development. Plus, data assembly creates a comprehensive petition dossier for all regulatory purposes.
  
• Final turn-key submission of citizen petition.
  
• Expert advice on how to maximize market opportunities within your chosen areas and beyond.