Contract manufacturing for medical devices under an ISO 13485-certified quality system.
ANAVERIS provides contract manufacturing and technology transfer for selected medical-device formats, including creams, gels, liquids, sprays and products specifically intended for cleaning or disinfecting medical devices. Each project is assessed according to its intended purpose, classification, manufacturing requirements and the responsibilities agreed with the Legal Manufacturer.
Manufacturing support for established medical-device projects.
Legal Manufacturers
Contract manufacturing within clearly defined technical and quality responsibilities.
Healthcare & Pharmaceutical Companies
Flexible manufacturing and long-term supply.
Established Healthcare Brands
High-quality production under certified quality systems.
Technology-Transfer Projects
Smooth transfer from existing manufacturers.
Selected medical-device categories we manufacture.
Manufacturing feasibility depends on intended purpose, classification, formulation, packaging system and agreed regulatory responsibilities.
Topical & Skin-Barrier Devices
✓ Medical creams
✓ Barrier creams
✓ Skin repair creams
Haemorrhoid-Care Devices
✓ Creams
✓ Gels
✓ Rectal formulations
Vaginal-Care Devices
✓ Vaginal gels
✓ Vaginal douches
✓ Specialized intimate medical products
Ear-Care Liquids
✓ Ear wax removal drops
✓ Ear cleansing solutions
✓ Medical ear care liquids
Nasal-Care Sprays
✓ Nasal sprays
✓ Saline sprays
✓ Moisturising nasal sprays
Hair & Scalp Devices
✓ Hair lice removal liquids
✓ Specialized scalp treatments
Breastfeeding-Support Devices
✓ Nipple care patches
✓ Breastfeeding support products
Device Cleaners & Disinfectants
✓ Surgical instruments
✓ Medical devices
✓ Medical equipment
✓ Clinical surfaces
Additional medical device product categories may be supported following technical evaluation and manufacturing feasibility assessment.
MEDICAL DEVICE DISINFECTANTS
Products for cleaning and disinfecting medical devices.
ANAVERIS manufactures products specifically intended for cleaning or disinfection of medical devices, including surgical instruments and medical equipment, where intended purpose and classification place them within the MDR. General clinical-surface disinfectants should not be presented as medical devices.
Manufacturing formats and packaging systems.
Creams & Gels
Compatible tubes, jars or airless packaging systems.
Medical Liquids
Selected plastic or glass packaging systems.
Medical Sprays
Compatible pumps and applicators for nasal, topical and specialist spray formats.
Device Cleaners & Disinfectants
Liquid products intended specifically for cleaning or disinfecting medical devices.
Clear responsibilities. Controlled manufacturing.
Within the agreed project scope, ANAVERIS supports technology transfer, scale-up, manufacturing, in-process controls, batch documentation and production planning.
MEDICAL DEVICE DISINFECTANTS
✓ Technology Transfer
✓ Manufacturing Feasibility
✓ Scale-Up Support
✓ Controlled Production
✓ Batch Documentation
✓ Supply Planning
Why medical-device companies choose ANAVERIS.
Contract manufacturing, technology transfer and documented production controls coordinated through one experienced project team.
ISO 13485-Certified QMS
A certified quality-management system.
Structured Technology Transfer
A controlled route into production.
Controlled Manufacturing
Defined parameters and in-process checks.
Documented Traceability
Connected records support traceability.
Flexible Production Planning
Planning aligned with agreed requirements.
Dedicated Project Coordination
One experienced coordination team.
Manufacturing under internationally recognised quality systems.
ANAVERIS operates an ISO 13485 certified Quality Management System supporting the manufacturing of medical devices in accordance with applicable regulatory requirements.
ISO 13485
ISO 9001
FDA Registered
GMP
FDA Registered Facility and GMP where applicable.
A structured path to transfer production.
We regularly support companies transferring production from existing manufacturers.
Confidential Project Review
Technical Documentation Review
Feasibility & Gap Assessment
Transfer & Scale-Up Plan
Verification / Validation Activities
Routine Production & Change Control
Quality controls designed for medical-device manufacturing
Documented procedures, trained personnel, material controls, defined manufacturing parameters, in-process checks, batch documentation, change control and traceability support controlled production.
Documented Quality System
Qualified People
Controlled Production
Tracebility & Change Control
Why global brands trust ANAVERIS.
Quality is not a final inspection. It is built into every step.
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.
Quality by Design
People & Training
Continuous Improvement
Compliance Assurance
Certifications & Facility Registrations
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
ISO 13485
Medical Devices QMS
GMP ComplianceScope and validity in the linked document
FACILITY REGULATIONS
Greece — EOF
Facility registered
Supplements, cosmetics, FSMPs and medical devices
United States — FDA
Food Facility registered
U.S. food-facility registration
United Arab Emirates
Registered manufacturer
Supplements and cosmetics
Practical value throughout your manufacturing project.
Clear Responsibilities
Robust quality systems help simplify customer qualification and regulatory submissions.
Structured Product Transfers
Manufacturing performed under internationally recognised quality systems.
Documented Production
Validated processes and in-process controls deliver reliable batch-to-batch consistency.
Consistent Process Controls
Stable manufacturing processes that support long-term business growth.
Supply-Continuity Support
Quality systems that support customers selling into multiple global markets.
Controlled Improvement
Ongoing monitoring and process optimisation ensure continuous enhancement of manufacturing performance.
Looking for an ISO 13485-certified contract manufacturing partner?
Whether you are transferring an existing product, expanding production capacity or evaluating an additional manufacturing site, our team can help you assess the next practical step.