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Serialization & Aggregation
The effective protection against counterfeiting through product coding,
serialization and aggregation of drugs (primary, secondary, and tertiary
packaging) has become a regulatory requirement in various markets.
Through intelligent and customer-oriented packaging line concepts, we meet the highest technical and organizational standards at all levels of coding, serialization and Aggregation and fulfill all market requirements. '
Since January 2015 we globally produce serialized and aggregated products with our highly adaptable system infrastructure to fulfil all present and new market Standards:
R-Pharm Germany GmbH
2015On CPhI since
- Selling PointsExperienced Technicians; International Approvals/Standards; Packaging; Small Orders Accepted
R-Pharm Germany GmbH
2015On CPhI since
More Products from R-Pharm Germany GmbH
15 Years of Experience in High Potent Manufacturing
To manufacture OEB 4-5 products, several segregated production units for different batch sizes - starting with 0.5 to 20 kg in the small scale facility or up to 700 kg in the Newcon - are available.
The "NEWCON" (New Containment Facility):
With the commissioning of this Facility, a major milestone in terms of automation, process robustness and process safety has been set worldwide. The production unit awarded as “Facility of the Year 2008” by ISPE and certified by the FDA sets standards in the application of a fully automated process flow of several batches in parallel.
The PPDC (Product and Process Development Center):
Beside cost-effective containment solutions for fully automated procedures, the PPDC allows us to expand our service portfolio in the area of high potent manufacturing and enables both, product development and commercial small-scale manufacturing.
Equipment used for High Containment process steps:
- Milling, mixing and sieving
- Dry and wet granulation
- Pelletizing, capsule filling, tableting
Whether blister, wallet, bottle or specialty packaging – we are able to specifically and flexibly meet the needs of customer and product requirements because of our broad range of packaging solutions and services. For this, we have 13 packaging lines in a multi-shift operation and a capacity of approximately 120 million sales units at your disposal.
For conventional manufacturing methods in the range OEB 1 to 3 and nutritional supplements, we have a highly flexible production facility at your disposal with 12,000 m2 on three levels with the most modern equipment and technology – including facilities for handling non-aqueous solutions (explosion proof).
We offer production services for various solid dosage forms in the best quality; capacity 5 billion, Solida production: tablets, hard capsules, powders, granules, pellets.
Quality is more than a standard in Illertissen, whether in in-house production or as a contract manufacturer. Our aim is to ensure that quality is already systematically secured within the process and to embed supreme standards as a contribution for process excellence.
Naturally, all documentation / data reporting is completed in accordance with current GMP guidelines.
> Quality Control
> Stability Studies
Which product is missing in your portfolio?
We bring your finished formulation as well as jointly developed formulations based on health claims to market maturity. Furthermore, we are pleased to present innovative concepts that expand your product portfolio in the shortest possible time. We listen carefully to your individual requirements and internal processes.
Discover our wide range of food supplements for various indications. We are looking forward to your inquiry.
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