Liquid Filling and Biosides
FMP produces a range of sterile and non-sterile medical devices, personal care and biocide liquid products in rigid plastic or glass containers.
How to decide whether you need specialist liquid filling
Specialist liquid filling is relevant when a medical, healthcare or biocide product needs to be filled under controlled conditions, with defined contamination controls, accurate metered volumes, suitable closures and the quality documentation required for its intended market.
FMP supports sterile and non-sterile medical devices and personal care liquids, biocides and disinfectants in formats ranging from small volume 10–100 mL presentations to medium volume 100–1000 mL bottles, including bag-in-bottle and trigger spray formats.
By partnering with FMP, you gain cleanroom filling, aseptic capability, packaging and closure expertise, technical file support and deep regulatory knowledge all within one manufacturing partner.
Sterile or non-sterile: which filling route should you choose?
The correct route depends on your product’s intended use, regulatory classification, formulation, contamination risk and method of application. FMP can help you assess these requirements and define the appropriate environment, filling process, closure and packaging route, before production begins.
Our capabilities
• Sterile and non-sterile liquid filling
• Aseptic processing where required
• Small-volume filling (typically 10–100 mL)
• Medium-volume filling (typically 100–1000 mL)
• Medical device and personal care liquids
• Biocide and disinfectant filling
• Technical file management
• ISO 13485 quality systems
Formats / variants
• Rigid plastic and glass containers
• Bag-in-bottle systems
• Trigger spray bottles
• Screw closures
• Crimp closures
• Snap-on closures
• Customer-specific labelling and presentation
How medical and biocide liquid filling works
Medical and biocide liquid filling requires controlled handling, accurate dosing, suitable container and closure systems, and documented quality controls.
FMP provides:
✓ Small- and medium-volume filling from approximately 10 mL to 1000 mL, depending on the product and format.
✓ Dedicated cleanroom filling for sterile and non-sterile liquids, with aseptic processing capability, where required.
✓ Bottle, bag-in-bottle and trigger spray presentations with screw, crimp and snap-on closure options.
✓ ISO 13485-controlled quality systems, regulatory documentation and technical file support for compliant manufacture.
FMP can also combine standard filling and packaging capabilities in novel ways to solve your specific requirements, including cleanroom-use products and multi-bagged presentations.
Medical and healthcare liquids
Controlled filling for medical device, healthcare and personal care liquids where accurate dosing, contamination control and compliant documentation are essential.
Biocides and disinfectants
Sterile and non-sterile biocide and disinfectant products for infection prevention, including bottle, spray and specialist cleanroom-use presentations.
Cleanroom-use solutions
Customer-specific products such as bag-in-bottle and double- or triple-bagged spray presentations developed for transfer and use within controlled environments.
The benefits of outsourcing liquid filling and biocides
Outsourcing liquid filling and biocide manufacture to FMP enables you to:
✓ Access dedicated cleanroom filling, aseptic capability and ISO 13485-controlled quality systems.
✓ Use specialist regulatory and technical file expertise for products entering highly regulated healthcare markets.
✓ Select from a range of bottle sizes, closure types and presentations without investing in dedicated filling infrastructure.
✓ Combine filling, packaging, labelling and customer-specific configuration within one controlled supply route.
✓ Scale from specialist medical applications to larger-volume production as demand develops.
FMP provides the manufacturing, packaging and compliance infrastructure needed to move your regulated liquid products from requirement to reliable market supply.
Enquiry
Consultation
Quote
Delivery
What to look for in a liquid filling and biocides partner
A liquid filling partner needs to offer more than available line capacity. For regulated healthcare and biocide products, look for a supplier that can connect controlled filling with formulation understanding, packaging compatibility, regulatory documentation and technical problem-solving.
FMP supports you with:
✓ ISO 13485-certified quality systems and dedicated cleanroom filling environments.
✓ Sterile and non-sterile filling plus aseptic capability where required.
✓ Deep regulatory expertise, documentation support and technical file management.
✓ Experience with medical device liquids, personal care products, biocides and disinfectants.
✓ Bottle sizes from approximately 10 mL to 1 litre with multiple closure and spray options.
✓ Development and packaging expertise for standard, private-label and customer-specific presentations.
We partner with you to combine proven manufacturing components into a solution matched to your product, market and compliance requirement.
FAQs
FMP fills sterile and non-sterile medical device liquids, personal care products, biocides and disinfectants. Applications include infection prevention and surface disinfection products as well as liquids used in medical and healthcare settings. Each enquiry is reviewed against the formulation, intended use, regulatory requirements and packaging format.
Yes. FMP can fill bag-in-bottle systems and trigger spray presentations, alongside standard bottles. Closure options include screw, crimp and snap-on fittings. The appropriate container and closure system is selected around product compatibility, dose, application and market requirements.
Typical small-volume metered doses range from 10 ml to 100 ml, while medium-volume filling for medical devices and biocides typically ranges from 100ml to 1000 ml. FMP can review requirements outside these typical ranges where the product and process are suitable.
Yes. Regulatory compliance and technical file management are established FMP capabilities. The team supports customers operating in highly regulated markets and can help define the documentation and manufacturing controls needed to maintain compliant supply within FMP’s ISO 13485 quality framework.
Yes. FMP has dedicated cleanroom capability for liquid-based sterile and non-sterile products and can support aseptic filling where required. The appropriate route is determined by intended use, regulatory requirements, formulation and contamination risk.
Start with an enquiry outlining the product and intended use, formulation status, regulatory classification, required volume, container and closure preference, expected production volumes and target market. FMP will review the technical and compliance requirements, define the appropriate route and provide a quotation before production.
