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Lomapharm® - Your contract manufacturing partner for solid and liquid pharmaceuticals

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Lomapharm Logo

We produce your tablets, film tablets and sugar-coated tablets, as well as liquids and sterile liquids, under GMP conditions. Our full service covers the whole range up to the final packaged product. Over 100 years of experience you can trust.
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As a medium-sized pharmaceutical company with around 00 employees, Lomapharm specialises in the production of solid and liquid pharmaceuticals.

Founded as long ago as 1878, this family-run company is now managed by the fourth generation. The company can look back on a long and proud tradition of pharmaceutical production.

Lomapharm today is one of three affiliated companies within the Lohmann Group located in Emmerthal in the Weserbergland near Hameln/Germany.

The core expertise of the Lohmann Group is processing and refining iron and mineral salts and their end products. The group has 500 employees overall and includes Lomapharm GmbH KG, Dr. Paul Lohmann GmbH KG and Neudorff GmbH KG.

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TABLETTING
Your specialist for tablets, sugar coated tablets and mineral-salt based products
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Our strength include the contract manufacturing of tablets and their further processing to film tablets or sugar-coated tablets. Lomapharm also specialises in the production and filling of liquids including sterile pharmaceuticals. All of our production complies with GMP standards.

The proactive investment strategy of the family that owns Lomapharm – now in its fourth generation – ensures that the company always fulfils the increasing demands of national and international markets.

In addition to the classic contract manufacturing of pharmaceuticals and food supplements in accordance with orders from clients, another speciality involves the production of iron and mineral salt based products in close co-operation with our affiliated company Dr. Paul Lohmann GmbH KG. The full service available to our clients today is based on over 100 years of experience.

Our services range from the procurement of raw materials all the way to the shelf-ready final packaged product – all customised to your specific requirements.

Our services include advice and customer care, starting with your original enquiry right through to delivery of your product. Our range of services is rounded off by a broad spectrum of additional services such as the development and galenic optimisation of formulations, and support in approval application procedures.

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SOLID PHARMACEUTICALS
High quality processing of all batches
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The versatile range of machines at our disposal not only enables us to produce mixtures for direct tablet production, but

also granulates – via dry granulation or wet granulation with subsequent drying. Tabletting is carried out by computer-controlled high capacity presses. Coating takes place in a range of drum coaters with up to 500 kg capacity, and modern tablet coating pans with capacities of up to 120 kg each. This enables us to process small and large batches of high quality sugar-coated tablets.

Mixing
- Free-fall mixers
- Compulsory mixers

Granulation
- Classic wet granulation
- Roller compaction

Tabletting
- 10 tabletting machines
- capacity of up to 250,000 tablets per hour

Sugar coating and film coating
- 18 sugar coating pans - some capable of automatic sugar coating
- Film coaters for different sized batches
- From classic film tablets to special forms, e.g. silver coated tablets

Capacities
Over 4 billion tablets per year of which more than 1 billion film-coated and approx. 2 billion sugar-coated tablets

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SOLID PHARMACEUTICALS
State-of-the-art technology for sophisticated filling
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When it comes to liquid pharmaceuticals, Lomapharm produces solutions and sophisticated suspensions in batches up to 2.9 t – also under nitrogen depending on the specific product. Modern filling lines ensure perfect filling. Final packaging and labelling takes place online under computer control – also for full wraparound functional labels.

Solutions - Syrups - Suspensions - Batches up to 2,900 kg

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STERILE PHARMACEUTICALS
Aseptic production – sterile production you can trust
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The manufacture of sterile products requires special care. Lomapharm has modern clean rooms which comply with the increasingly stringent specifications laid down for sterile production. The filling line fills ampoules and eye-drops up to 10 ml in size, which are usually prepared by us in medium-sized batches.

Sterile solutions in batches up to 650 kg - Ampoule filling (1-10 ml) - under aseptic conditions including end sterilisation - Filling of eye-drops (5-10 ml) - Clean room classification A

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PACKAGING

Customised, environmentally-compatible and optimally controlled
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We have a whole range of packaging options available for the optimal packaging of your products. The spectrum ranges from blister packs manufactured at up to 100,000 tablets

per hour, to packaging in ampoules in customised and environmentally -compatible trays.

We use a whole series of control systems to ensure that your products are flawlessly packaged.

Powders and granulates
- Sealed edge bags/ sachets up to 35 g
- Containers (metal/plastic)
- Bottles

Tablets
- Blister
- Containers (metal/plastic)
- Bottles

Liquids
- Sealed edge bags/ sachets
- Bottles up to 500 ml

Final packaging
- Folding cartons or clinic packages
- Ampoules in environmentally friendly corrugated paper tray units.
- Complete monitoring by automatic in-process control systems

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SERVICES
Our service has an extra plus: Our long experience to back up your innovation
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Maintaining high quality standards can only be guaranteed by permanent quality control. Our highly qualified team of laboratory staff provide the whole range of control services – from raw material testing to stability testing pursuant to GMP and ICH regulations.

One of our key areas of expertise is the analysis of vitamins and minerals. Our expertise and experience is also on call for galenic development and optimisation.We will also be happy to provide you with assistance in your approval projects.


Analysis

- Chemical and physical analysis of raw materials, intermediate and end products, pursuant to national and international specifications and customer-specific specifications
- Microbiological purity
- Stability testing and sample storage pursuant to ICH regulations

Development
- Galenic development
- Development, validation and optimisation of formulations and production processes
- Development and validation of test methods
- Scaling up new products from lab production to industrial production

Approvals and registration
- Elaboration of approval documentation /registration dossiers pursuant to national/international regulations
- CTD formats

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Want to know more?
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To request information, please use the request box on the right of this page.

|In June 2008, this company's services were awarded product of the month by Pharmaceutical Manufacturing News Editors|

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