Preclinical Formulation Analysis Services

The accuracy, and reliability of preclinical formulation is essential for drug development and safety. Porsolt, a dedicated provider of preclinical Contract Research Organization (CRO) services, delivers a comprehensive suite of formulation analysis capabilities. Our expertise reflect our commitment to the success of your project, ensuring meticulous attention to every detail in the drug development process.


Comprehensive Formulation Analysis Capabilities

Porsolt’s formulation analysis capabilities are meticulously crafted to ensure the concentration, stability, and homogeneity of your formulations, essential for successful preclinical studies. This includes detailed concentration verification of active pharmaceutical ingredients (APIs), crucial for the solubility and activities of your drug, thereby ensuring it delivers its intended therapeutic effect with precision.

Method Development and Transfer Tailored to Your Needs

Our team is adept in developing and transferring analytical methods, with a keen focus on specificity and accuracy, vital for the integrity of preclinical studies. These methods are carefully tailored to meet the unique requirements of your project, ensuring seamless integration.

This approach is a key aspect in advancing your preclinical development program.

Rigorous Method Validation for Dependable Results

Method validation is a critical aspect of our GLP safety services. We conduct comprehensive validation, focusing on key parameters such as linearity and precision. This rigorous approach ensures that our methods adhere to regulatory standards and are robust and reliable, catering specifically to your application’s needs.

Stability Evaluation: A Key Component of Formulation Analysis

Understanding the stability of your formulation under various conditions is essential. We perform detailed stability evaluations for both stock and dosing formulations. This analysis is pivotal in determining the shelf life and optimal storage conditions, and safeguarding the integrity of your drug throughout its lifecycle.

Adsorption Evaluation for Enhanced In Vitro Studies

In vitro studies are an integral component of preclinical development. Our adsorption evaluation services meticulously examine how your formulation interacts with biological systems. This analysis is vital in comprehending the properties of your drug, a cornerstone of our formulation approach, and is essential for determining its bioavailability and efficacy.

Homogeneity Testing for Consistent Drug Formulations

Uniformity in drug formulations is vital for consistent therapeutic effects. Our formulation analysis includes stringent testing to ensure homogeneity. This guarantees that each dosage unit of your drug is consistent in composition and efficacy, a critical factor for the success of clinical trials and market approval.

Your Strategic Partner in Preclinical Formulation

At Porsolt, we are committed to being more than just a service provider; we are your strategic partner in drug development. Our dedication to excellence in preclinical formulation analysis is steadfast. We recognize the complexities and challenges of this phase and are dedicated to providing solutions that meet and surpass your expectations.

Partner with us for a significant stride towards the successful development of your pharmaceutical products.


Z.A. de Glatigné
53940 Le Genest-Saint-Isle, France
Telephone +33 2 43 69 36 07

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