Contract manufacturing for established PT1 products.
ANAVERIS manufactures selected human-hygiene disinfectants intended for application to human skin. We support established formulations and structured technology transfers, with flexible sourcing, packaging and documented production controls.
We do not develop new disinfectant formulations.
Product Type 1 covers biocidal products used for human-hygiene purposes and applied on, or brought into contact with, human skin or the scalp primarily to disinfect.
Manufacturing projects are assessed in the context of the applicable Biocidal Products Regulation requirements and the product’s intended market. Examples include:
✓ Alcohol Hand Sanitiser Gel
✓ Chlorhexidine-based formulations
✓Alcohol Hand Sanitiser Lotion
✓ Isopropyl Alcohol formulations
Product Type 1 (PT1) – Human Hygiene
Disinfectants intended exclusively for application on human skin.
Selected formats for human hygiene.
Alcohol-Based Hand Gels
Ethanol- or isopropanol-based gels manufactured to agreed product and process specifications.
PACKAGING
Plastic tubes · Flip-top bottles · Pump bottles · Sachets
Alcohol-Based Liquids
Ethanol- or isopropanol-based liquids and lotions for human-hygiene applications.
PACKAGING
Plastic bottles · Pump bottles · Spray bottles
Selected Cleansing Liquids
Selected chlorhexidine digluconate cleansing liquids may be considered following confirmation of product classification, intended claims, authorisation status and target market.
PACKAGING
Plastic bottles · HDPE bottles · 5 L HDPE jerrycans
Packaging Solutions
Packaging selection and line compatibility are reviewed as part of every manufacturing project.
PACKAGING
Tubes · Bottles · Pumps · Flip-tops · Sprays · Sachets · 5 L HDPE jerrycans.
A manufacturing model adapted to your project.
Choose the sourcing and manufacturing model that best matches your formulation, supply chain and existing product status.
Turnkey Manufacturing
We source agreed raw materials and packaging components against the agreed project specification.
Hybrid Manufacturing
Responsibilities are divided between your team and ours according to the requirements of the project.
Customer-Supplied Materials
Manufacturing using agreed customer-supplied raw materials, active substances or packaging components.
Technology Transfer
A structured transfer of established formulations, specifications and manufacturing processes.
A focused European manufacturing partner.
Focused PT1 manufacturing capabilities, flexible project models and one coordinated team.
PT1 Manufacturing Focus
Manufacturing scope and batch size assessed against the agreed product and available capability.
Flexible Sourcing
One team coordinating technical review, sourcing, production and delivery requirements.
Documented Production Controls
Manufacturing supported by agreed specifications, in-process controls and batch records.
Structured Technology Transfer
Turnkey · Hybrid · Customer-supplied materials.
Multiple Packaging Formats
Manufactured under internationally recognised quality systems.
Dedicated Project Coordination
Manufacturing in Greece for agreed customer markets and project requirements.
Looking for a disinfectant intended for medical devices?
Products specifically intended to clean or disinfect medical devices follow a different regulatory pathway and should not be presented as PT1 human-hygiene products.
Quality systems that support controlled manufacturing.
Quality is incorporated throughout supplier review, incoming-material control, manufacturing, packaging, batch documentation and traceability.
From supplier qualification and incoming inspection to manufacturing, in-process controls, batch release and full traceability, ANAVERIS operates internationally recognised quality systems that support reliable manufacturing across multiple regulated healthcare product categories.
Agreed Specifications
In-Process Controls
Batch Documentation
Traceability
Quality systems and manufacturing documentation.
We are committed to the highest international standards of quality, safety and regulatory compliance.
ISO 22000:2018
Food Safety Management System
ISO 9001:2015
Quality Management System
GMP ComplianceScope and validity in the linked document
CILITY REGULATIONS
Greece — EOF
Facility registered
Supplements, cosmetics, FSMPs and medical devices
United Arab Emirates
Registered manufacturer
Supplements and cosmetics
What this means for your business
Defined Manufacturing Scope
Robust quality systems help simplify customer qualification and regulatory submissions.
Consistent Batch Execution
Manufacturing performed under internationally recognised quality systems.
Consistent Product Quality
Validated processes and in-process controls deliver reliable batch-to-batch consistency.
Reliable Long-Term Partner
Stable manufacturing processes that support long-term business growth.
International Market Access
Quality systems that support customers selling into multiple global markets.
Continuous Improvement
Ongoing monitoring and process optimisation ensure continuous enhancement of manufacturing performance.
Looking for a PT1 manufacturing partner?
Tell us about the formulation type, active substances, current authorisation status, packaging format and intended market. Our team will review the available technical information and help define the appropriate manufacturing route.
📋 Manufacturing under certified quality systems