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SciQra- Mastering Toxicology Through Scientific Minds
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SciQra- Mastering Toxicology Through Scientific Minds
SciQra- Mastering Toxicology Through Scientific Minds
Home
Why SciQra
Team
Locations
Cosmetics & Consumer Products
Pharmaceuticals
Medical Devices
Food & Supplements
Petcare & Veterinary
Household & Hygiene
Chemicals
Toxicological Assessment
Regulatory Compliance
Clinical Testing
Scientific Writing
California Prop 65
Hazard Assessment
Data-Gap Analysis
Raw Material Selection
GRAS Determination
Preclinical Testing
Claim Substantiation
Impurity Qualification
Health-Based Exposure Limits (PDE & OEL)
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Hazard Assessment
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Featured
Medical Device Toxicological Risk Assessment in the USA: ISO 10993, Extractables & FDA Compliance Explained
SciQra LLC
Feb 9, 2026
Medical Device Toxicological Risk Assessment in the USA: ISO 10993, Extractables & FDA Compliance Explained
SciQra LLC
Feb 9, 2026
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Feb 9, 2026
From Ingredient Review to FDA Safety: Toxicology for Dietary Supplements in the USA
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Feb 6, 2026
From Ingredient Review to FDA Safety: Toxicology for Dietary Supplements in the USA
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Feb 6, 2026
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Feb 6, 2026
Hazard Assessment & PDE OEL Services in USA | Toxicology Experts
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Jan 27, 2026
Hazard Assessment & PDE OEL Services in USA | Toxicology Experts
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Jan 27, 2026
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SciQra LLC
Jan 27, 2026
Chemical Product Safety in the USA: Toxicology-Based Regulatory Compliance
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Jan 23, 2026
Chemical Product Safety in the USA: Toxicology-Based Regulatory Compliance
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Jan 23, 2026
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Jan 23, 2026
GRAS Determination in the USA: FDA Requirements and Regulatory Pathway
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Jan 23, 2026
GRAS Determination in the USA: FDA Requirements and Regulatory Pathway
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Jan 23, 2026
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Jan 23, 2026
Clinical Testing Support in the USA: Toxicology-Led Strategy & CRO Collaboration
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Jan 17, 2026
Clinical Testing Support in the USA: Toxicology-Led Strategy & CRO Collaboration
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Jan 17, 2026
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Jan 17, 2026
Pharmaceutical Regulatory Compliance in the USA - The Role of Toxicology
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Jan 16, 2026
Pharmaceutical Regulatory Compliance in the USA - The Role of Toxicology
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Jan 16, 2026
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Jan 16, 2026
Preclinical & Regulatory Toxicology Consulting: Turning Science into Regulatory Confidence
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Jan 2, 2026
Preclinical & Regulatory Toxicology Consulting: Turning Science into Regulatory Confidence
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Jan 2, 2026
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Jan 2, 2026
Toxicological Risk Assessment of Medical Device in Accordance with  ISO 10993
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Dec 27, 2025
Toxicological Risk Assessment of Medical Device in Accordance with  ISO 10993
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Dec 27, 2025
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Dec 27, 2025
Global Cosmetic Safety - How CPSR Supports EU Compliance and US MoCRA Readiness
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Dec 26, 2025
Global Cosmetic Safety - How CPSR Supports EU Compliance and US MoCRA Readiness
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Dec 26, 2025
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Dec 26, 2025
Unlocking the Regulatory Requirements for EU Cosmetic Market
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Dec 19, 2025
Unlocking the Regulatory Requirements for EU Cosmetic Market
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Dec 19, 2025
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Dec 19, 2025
Product Information File (PIF) – Access Market with Document Excellence
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Dec 18, 2025
Product Information File (PIF) – Access Market with Document Excellence
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Dec 18, 2025
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Dec 18, 2025
Product Safety Consulting in USA for Regulatory Compliance and Risk Control
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Dec 9, 2025
Product Safety Consulting in USA for Regulatory Compliance and Risk Control
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Dec 9, 2025
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Dec 9, 2025
Scientific Writing in the USA for Research Papers, Reports, and Documentation
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Dec 2, 2025
Scientific Writing in the USA for Research Papers, Reports, and Documentation
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Dec 2, 2025
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Dec 2, 2025
Cosmetics Safety in USA: Compliance Support for Safe Product Launches
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Dec 2, 2025
Cosmetics Safety in USA: Compliance Support for Safe Product Launches
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Dec 2, 2025
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Trusted Hazard Identification Consultants Across the USA
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Nov 26, 2025
Trusted Hazard Identification Consultants Across the USA
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Nov 26, 2025
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Nov 26, 2025
Trusted Toxicological Risk Assessment Experts for the USA & Europe
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Nov 26, 2025
Trusted Toxicological Risk Assessment Experts for the USA & Europe
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Nov 26, 2025
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Nov 26, 2025
Smart Product Safety Solutions for Leading Skincare Brands in the USA & Europe
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Nov 18, 2025
Smart Product Safety Solutions for Leading Skincare Brands in the USA & Europe
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Safety Substantiation and CPSR Made Easy – Fast Cosmetics Compliance in the USA & Europe
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Nov 17, 2025
Safety Substantiation and CPSR Made Easy – Fast Cosmetics Compliance in the USA & Europe
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Reliable Toxicological Risk Assessment for Extractables and Leachables in the USA and Europe
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Nov 14, 2025
Reliable Toxicological Risk Assessment for Extractables and Leachables in the USA and Europe
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Nov 14, 2025
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Ensure Safer Supplements with Expert Safety Assessment
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Nov 14, 2025
Ensure Safer Supplements with Expert Safety Assessment
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Nov 14, 2025

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Cosmetic Product Safety Report (CPSR) – What It Includes and Why It Is Required
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Jun 27, 2025
Cosmetic Product Safety Report (CPSR) – What It Includes and Why It Is Required
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Jun 27, 2025
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Immediate vs Delayed Toxicity: Why Knowing Your Exposure Timeline Matters
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Jun 26, 2025
Immediate vs Delayed Toxicity: Why Knowing Your Exposure Timeline Matters
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Jun 26, 2025

This Blog post contains information regarding Immediate vs Delayed Toxicity

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Local vs Systemic Toxicity of Drugs
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Jun 18, 2025
Local vs Systemic Toxicity of Drugs
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Botulinum Toxin: Deadliest to Useful
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Apr 29, 2025
Botulinum Toxin: Deadliest to Useful
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Apr 29, 2025

Botulinum toxin, the most lethal substance known to science has an LD50 (lethal dose 50) of merely 1 nanogram per kilogram of body weight.

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Apr 29, 2025
When Water Becomes a Threat 
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Apr 27, 2025
When Water Becomes a Threat 
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Despite being an essential part of daily life, water can become toxic when consumed excessively or inappropriately.

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Paracelsus’ Legacy Echoes Through Time
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Apr 12, 2025
Paracelsus’ Legacy Echoes Through Time
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Apr 12, 2025

“All things are poison, and nothing is without poison; only the dose makes a thing not a poison.” These words laid the groundwork for modern toxicology.

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Apr 12, 2025

At SciQra, a leading Toxicology Consulting Partner, we deliver expert Toxicological Risk Assessment and Regulatory Support for Cosmetics, Medical Devices, Pharmaceuticals, Dietary Supplements, Consumer Products, and Chemicals. Our expertise includes Cosmetic Product Safety Report (CPSR) Preparation, Product Information File (PIF) Compilation, Cosmetic Ingredients Safety Evaluation, Systemic Exposure Calculation, Margin of Safety (MoS) Derivation, and Impurity Qualification. Whether you require a Biocompatibility Gap Assessment aligned with ISO 10993 and FDA standards for Medical Devices, or Raw Material Safety Evaluation for Cosmetic Products, our team ensures compliance with Global Safety and Regulatory Requirements.

We also support global brands with Hazard Identification, GRAS Determinations, Claim Substantiation, Toxixological Risk Assessment of Extractables & Leachables (E&L), Preclinical Documents for IND/CTA Submission, and Health-based Exposure Limit (PDE/OEL) Determinations. From EU Cosmetic Regulation (EC) No 1223/2009 compliance to USFDA’s MoCRA Requirements, SciQra bridges regulatory expectations across markets to deliver robust compliance solutions.

With a strong focus on Cosmetic and Consumer Product Toxicology Assessment and Regulatory Support, SciQra helps businesses launch safe, effective, and compliant products worldwide. Whether you need an expert opinion on Prototype Formula, Cosmetic Safety Certification, Dietary Supplement Safety Evaluation, or Regulatory Toxicology Strategy for global product launches, we deliver science-driven, tailored solutions.

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SciQra LLC is a science-based consulting firm that utilizes data-driven strategies to solve complex issues across a variety of industries.

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14 Brewster Cir
Old Bridge, NJ 08857

Phone: +1 609 917 6181
Email: contact us

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