C.P.M. ContractPharma
GmbH & Co. KG

A Temmler Group company

Besides the production of semi-solid and liquid pharmaceutical dosage forms, the C.P.M. sites in Feldkirchen and Bruckmühl are also responsible for the entire product development and support processes up to marketing authorisation. C.P.M. ContactPharma became an affiliate of the Temmler Group for the express purpose of expanding its current capacities and to increase its flexibility. A highly qualified and dedicated workforce, state-of-the-art technologies and highly flexible production capacities are our core competencies and a guarantee for high-quality manufactured products. The FDA-certified site in Feldkirchen and the facility in Bruckmühl employ a workforce of 150 who, as an inherent part of the Temmler Group, show exemplary commitment in implementing customer requirements.

As your competent partner in contract manufacturing, we also specialise in the following:

Pharmaceutical dosage forms

• Semi-solid dosage forms (ointments, creams, gels, pastes, liposomes etc.)
• Liquid dosage forms (solutions, juices, sirups, tinctures, emulsions, lotions, suspensions, liposomes etc.)

Established manufacturing technologies

• Manufacture of semi-solid pharmaceutical forms (ointments, creams, gels, pastes etc.)
• Manufacture of liposomal preparations and nanotechnology
• Manufacture of liquids (solutions, tinctures, emulsions, lotions, suspensions, liposomes etc.)

Primary and secondary packaging of semi-solid pharmaceutical forms

• Filling of cylindrical and conical aluminum tubes
• Filling of plastic and polyfoil tubes
• Filling of dispensers and applicators
• Filling of jars and containers made of plastic or glass

Primary and secondary packaging of liquid pharmaceutical dosage forms

• Filling of glass and plastic containers
• Filling of pump sprays

Primary and secondary packaging of solid pharmaceutical dosage forms

• Blister packs (Alu/PVC/PVDC/PP/ARCLAR/TRIPLEX/COC)
• Bottling of bulk materials (glass bottles or plastic containers)
• Manual and special packaging (sample packs with individual blisters, repacking tasks, follow-up controls, deblistering etc.)

Development

• Development of semi-solid and liquid pharmaceutical forms with scale up options of 1 kg, 5 - 20 kg, 50 - 70 kg and up to 1,200 kg
• Coordination of internal and external projects for nanoparticle development
• Procurement of marketing authorisation dossiers and marketing authorisations
• Development of new dosage and packaging forms

Other services (selection)

• Analysis development
• Import, import analytcis and release
• Stability tests (ICH, on-going)
• Compilation of dossiers (insbesondere CMC part)
• GMP audits on behalf of the client