Questionnaire To Manufacturers for Endotoxin Testing Methods

Introduction

Endotoxin testing is essential for ensuring the safety of injectable pharmaceutical products by detecting potentially harmful bacterial toxins.


Traditional gold standard method, the Limulus Amebocyte Lysate (LAL) test, utilizes horseshoe crab blood for endotoxin detection. However, use of horseshoe crab blood led to the decline in horseshoe crab population and now poses a significant threat to the sustainability of LAL test impacting the medical field by potentially jeopardizing the safety of pharmaceutical products and posing a significant threat to public health. Advancements in technology have introduced alternatives, notably the recombinant Factor C (rFC) assay, which offers a sustainable and ethical alternative by eliminating the need for horseshoe crab blood.


This survey aims to review current endotoxin testing methods and assess the potential for the rFC method to be adopted by manufacturers in Low- and Middle-Income Countries (LMICs). By evaluating the benefits and challenges of rFC technology, this survey seeks to provide valuable insights into how LMIC manufacturers, regulators and stakeholders might navigate the transition to this innovative method, enhancing their testing capabilities while addressing global sustainability and ethical considerations.


The outcome of the survey will be shared in a webinar where you will be invited to participate.


Where is your company located?

Are you using LAL Test?
How satisfied are you with the cost of the LAL endotoxin testing method?
How satisfied are you with the sensitivity and specificity of LAL endotoxin test?
Are you aware of the recombinant Factor C (rFC) method for endotoxin testing?
Have you experienced any specific technical difficulties with rFC tests?
How satisfied are you with the sensitivity and specificity of the rFC endotoxin test?

Is your organization currently involved in the production or distribution of rFC endotoxin tests?
How would you rate the current level of competition in the rFC market?

How likely are you to adopt the rFC method in the near future?

If you had to choose today, what would you prefer for endotoxin testing?
Given the regulatory landscape in your country, how willing is your company to invest in conducting validation tests or studies to meet the requirements for rFC testing in the pharmacopoeia?

Thank you for completing this survey.

Your feedback is crucial for understanding and addressing the challenges associated with the adoption of rFC endotoxin testing.