Laboratory analysis and characterization of medical powders

Chemical analysis Characterization of materials R&D support
More than 140 people
More than 140 people at your service
5200 m² laboratory
5200 m² laboratory + 99% of services are provided in-house
Accredited laboratory
Accredited laboratory COFRAC ISO 17025

You want to carry out an analysis or characterization of medical powders

The FILAB laboratory supports pharmaceutical manufacturers and medical devices in the analysis of medical powders.

Thanks to a wide range of analytical techniques, we characterize the physical, chemical, morphological and rheological properties of the powders to guarantee their quality, their performance and their compliance.

What is a medical powder?

A medical powder is an assembly of solid heterogeneous particles dispersed in a continuous gaseous phase between which is exerted a multitude of interactions. Thus, depending on the nature of the powder and its properties, reactions with its environment can be endless. It is therefore essential to characterize the physico-chemical properties of a powder in order to best exploit it in the production process.

Physico-chemical properties to characterize a powder

The physico-chemical properties of powders influence their quality and performance.

Here are some examples of parameters that can be analyzed on a powder:

Crystallinity

Morphology

Granulometry

Humidity level

Specific surface

Chemical composition 

Density

Coulability

Medical powders applications

Medical powders are a very common and versatile form, whose uses extend far beyond simple powder for cutaneous application. Their role is central to both the pharmaceutical (drug) and medical device sectors.

In pharmacy

Powder is the basis of many forms of drugs. They are used in several ways:

  • Powders for oral solutions or suspensions
  • Powers for injections
    Inhalation powders
  • Powders for skin applications
  • Manufacturing of solid forms

In medical devices

Powder play a crucial role in the design and manufacture of various medical devices, often less visible for the public.

  • Implant materials
  • Additive manufacturing (3D printing)
  • Coatings and surfaces
  • Components of administration systems

FILAB supports manufacturers in the analysis or characterization of medical powders

Why choose FILAB for medical powder analysis?

For over 30 years, FILAB laboratory has had the experience and specific analytical fleet needed to be able to assist industrial companies in characterizing the physicochemical properties of powders using various techniques.

Assistance from an expert laboratory such as FILAB will allow you to better understand the strategic challenges you are facing as well as the changes in your field.

Our medical powder analysis and characterization services

Our services

ICP

GC-MS

XRD

SEM-EDX

BET

Laser Granulometry

FAQ

What is medical powder analysis?

Medical powder analysis is a set of laboratory techniques that aim to characterize the composition, physical properties, and purity of powders used in the manufacture of drugs and medical devices. This analysis is crucial to ensure the efficacy, safety, and compliance of products.

How is the chemical composition and purity of the powder checked?

For composition and purity, analyses focus on:

  • Identity of the active ingredient: ensuring that the powder is indeed the expected product.
  • Content (dosage): measuring the exact concentration of the active ingredient.
  • Presence of impurities: detecting synthetic by-products, residual solvents, or contaminants.
Is powder analysis the same for drugs and medical devices?

The principle is the same (characterizing the powder), but the parameters and techniques may differ. For a drug, the focus is on dosage, stability, and absorption. For a medical device (e.g., powder for 3D printing), the focus will be on the purity of the material, its biocompatibility, and its mechanical and sintering properties.

What are the specifications that powders must meet?

Each powder must comply with a set of specifications (acceptable limits) defined in its manufacturing file, in accordance with pharmacopoeial monographs (such as the European or American Pharmacopoeia). These specifications are validated by health authorities and guarantee the quality and consistency of the finished product.

The filab advantages
A highly qualified team
A highly qualified team
Responsiveness in responding to and processing requests
Responsiveness in responding to and processing requests
A COFRAC ISO 17025 accredited laboratory
A COFRAC ISO 17025 accredited laboratory
(Staves available on www.cofrac.com - Accreditation number: 1-1793)
A complete analytical park of 5,200m²
A complete analytical park of 5,200m²
Tailor-made support
Tailor-made support
Anaïs DECAUX Customer Support Manager
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