Personal Protective Equipment (PPE)

Assessment of PPE performance and safety, including filtration efficiency, breathability, and microbiological testing. These services ensure compliance with technical standards and applicable regulatory requirements.

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Intro

Assessment of PPE performance and safety, including filtration efficiency, breathability, and microbiological testing. These services ensure compliance with technical and regulatory standards while protecting end users. Sample types include respirators (FFP1, FFP2, FFP3), gloves, chemical protective garments, and safety eyewear.

Why perform this service

Health safety

Protection of human health through the early detection of microbiological, chemical and environmental risks, preventing incidents, outbreaks and undue exposures.

Legal compliance

Ensuring compliance with applicable national and European legislation and standards, through accredited analyses and adequate technical support.

Risk management

Identification, assessment and preventive mitigation of critical risks before they become non-conformities, incidents or operational impacts.

Operational optimization

Improvement of process efficiency through continuous monitoring, allowing to adjust practices, optimize resources and reduce operational costs.

Brand reputation protection

Reducing the risk of incidents with public or media impact, contributing to the confidence of consumers, customers and partners.

Decision-making support

Provision of reliable, traceable and technically validated data that support informed decisions at the technical, operational and management level.

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Types of analyses performed

They consist of carrying out laboratory tests that make it possible to assess the physical properties of materials and products, such as strength, permeability, or behavior under different conditions. These tests are essential to verify performance, quality, and compliance with regulatory and standard requirements.

Laboratory tests that detect, identify and quantify microorganisms (bacteria, fungi, yeasts, parasites and others) to evaluate the safety and quality of products and environments.

Delivery process

1

Sampling plan

Definition of strategic collection points and frequency of analyses according to the needs of each client.

2

Parametric values

Legal limits established for each parameter, based on public health and environmental quality criteria.

3

Periodic reports

Obligation to communicate the results to the competent authorities and to the public, where necessary.

Applicable legislation

Biogerm is accredited by IPAC according to the NP EN ISO/IEC 17025 standard for various water tests.

EN 149: 2001 + A1:2009
EN 14126:2003