Endotoxin Testing Services
Endotoxin Testing Services

Endotoxin Testing Services

Price 199 INR/ Piece

MOQ : 1 Piece
 

Endotoxin Testing Services Trade Information

  • Minimum Order Quantity
  • 1 Piece
  • FOB Port
  • Ahmedabad
  • Payment Terms
  • Cash Advance (CA), Cash in Advance (CID)
  • Delivery Time
  • 7 Days
  • Sample Policy
  • Contact us for information regarding our sample policy
  • Packaging Details
  • ANY
  • Main Export Market(s)
  • Asia, Australia, Central America, North America, South America, Eastern Europe, Western Europe, Middle East, Africa
  • Main Domestic Market
  • All India
  • Certifications
  • ISO
 

About Endotoxin Testing Services

Akshar Analytical Laboratory & Research Center is deeply committed to offering superiorEndotoxin Testing Servicesin order to satisfy the many needs of our valued customers. Our professionals oversee the performance of this service, ensuring that it meets all quality requirements set out by prominent industries. Our highly skilled personnel employ the greatest equipment and cutting edge technologies to provide this service. Additionally, the provided service is extremely dependable and executed in accordance with the established quality standards...



Advanced LAL Endotoxin Testing Expertise

Our facility utilizes Limulus Amebocyte Lysate (LAL) testing to precisely determine endotoxin levels in a wide range of products, from pharmaceuticals to medical devices. Certified personnel ensure accurate, reliable, and compliant analysis, supporting quality control and regulatory submissions. Accredited to ISO/IEC 17025:2017, our processes align with international standards, guaranteeing confidence in your results.


Wide Sample Acceptance and Fast Turnaround

We accept diverse sample types, including water, parenterals, biologics, pharmaceuticals, and medical devices, requiring only 2 ml per sample. With a robust workflow and state-of-the-art equipment, we deliver comprehensive results within just 5 working days, expediting your development timeline and regulatory processes.

FAQs of Endotoxin Testing Services:


Q: How are endotoxin levels measured in your testing services?

A: Endotoxin levels are quantified using the Limulus Amebocyte Lysate (LAL) test method, which is recognized for its sensitivity and specificity. Our laboratory performs both quantitative and qualitative determinations to ensure precise analysis of each sample.

Q: What sample types can I submit for endotoxin testing?

A: We accept water, parenteral solutions, biologics, medical devices, and pharmaceutical products for endotoxin analysis, provided each sample meets the minimum volume requirement of 2 ml.

Q: When will I receive the test results after submitting samples?

A: Results are typically provided within 5 working days of sample receipt. You will receive detailed reports in both digital and hard copy formats, facilitating documentation and regulatory compliance.

Q: Where is your testing conducted and what standards do you follow?

A: All testing is performed in our ISO/IEC 17025:2017 accredited facility in India, strictly adhering to USP, EP, and JP guidelines for endotoxin analysis to ensure global regulatory alignment.

Q: What is the process for submitting samples for testing?

A: Simply prepare your sample according to our requirements, ensuring a minimum of 2 ml. You can ship or deliver samples directly to our certified laboratory. Our team will communicate next steps and result timelines upon receipt.

Q: What are the benefits of using your endotoxin testing services?

A: Clients benefit from rapid turnaround, high assay sensitivity (detection range: 0.01 to 100 EU/ml), international compliance, and analysis performed by certified professionals. This ensures reliable results and stronger regulatory confidence.

Q: How can endotoxin testing be used in product development or launch?

A: Endotoxin testing is essential for verifying product safety, supporting batch release, validating manufacturing processes, and ensuring regulatory compliance, all of which are critical for successful development and commercialization of pharmaceuticals and medical devices.

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