Company Information (short)
Company Presentation (short)
Certificates (GMP / FDA)
Manufacturing authorization for veterinary medicinal products 2023
Equipment List
Publications
- Qualification of laboratory equipment: Perlick, Limberger; Pharm. Ind. 80, No. 7, 971-974, 2018
- Material and equipment in the pharmaceutical laboratory: Fuchslueger, Limberger, Perlick, Maas & Peither AG – GMP Verlag
- GMP-compliant handling of substances, devices and systems: Fuchslueger, Limberger, Perlick; Maas & Peither AG – GMP Verlag, 2018
- Chapter 14 “Quality control”, subchapter “Qualification of laboratory equipment”, Perlick C., Limberger M., Maas & Peither AG – GMP Verlag, 2017
- Papierbasierte und elektronische Dokumentation im Pharmaunternehmen, Anforderungen an GMP-konforme Dokumentationssysteme, Maas & Peither AG – GMP Verlag, 2017
- Safety assessment of excipients (SAFE) for orally inhaled drug products, Julia Katharina Metz, Lara Scharnowske, Fabian Hans, Sabrina Schnur, Katharina Knoth, Horst Zimmer, Markus Limberger, Henrik Groß, Claus Michael Lehr, Marius Hittinger
- Solid phase extraction as an innovative separation method for measuring free and entrapped drug in lipid nanoparticles, Alexis Guillot, Anne-Claude Couffin, Xavier Sejean, Fabrice Navarro, Markus Limberger and Claus-Michael Lehr
- Core processes in the pharmaceutical laboratory: GMP-compliant analysis from sampling to documentation, Maas & Peither AG – GMP-Verlag, 2016
- Particles in pharmaceutical production, F. Stienecker (ed.), Editio Cantor Verlag, 2015, Chapter 2, Particle measurement from R&D to GMP, state of the art and use in development and quality control – regulatory requirements, J. Schichtel, A. E. Türeli, M. Limberger
- Shelf Life of Reagents, Position paper proposed by the expert group „Pharmaceutical Analysis and Quality Assurance“ of the APV, Pharm.Ind. 77, Nr.12, 1788-1790 (2015)
- Chapter 14 “Quality control”, subchapter 14B “Substances in the laboratory, GMP consultant, Maas & Peither AG, GMP Verlag, 2015
- Good Documentation Practice in the Laboratory, Dr. M. Limberger, Part 1: Pharm.Ind. 77, No.10, 1522-1524 (2015), Part 2: Pharm.Ind. 77, No.12, 1774-1775 (2015)
- The Transfer of Analytical Procedures; Ermer J., Limberger M., Lis K., Wätzig H., Journal of Pharmaceutical and Biomedical Analysis (85), 2013
- GMP Advisor, Chapter 14 “Quality control”, Subchapter 14G “Out-of-specification results (OOX results), Maas & Peither AG, GMP Verlag, 2014
- In-situ Drug Release Monitoring with a Fiber Optic System, Guillot A., Limberger M., Krämer J., and Lehr C.M., Dissolution Technologies, Volume 20, Issue 2, may 2013
- A new concept for in vitro drug release testing of micro- and nanoformulations using a fiber optic system and derivative spectrophotometry, Alexis Guillot, Christina Draheim, Markus Limberger, Steffi Hansen and Claus-Michael Lehr, Submitted to International Journal of Pharmaceutics
- Solid phase extraction as an innovative separation method for measuring drug load and release from lipid nanoparticles, Alexis Guillot, Anne-Claude Couffin, Xavier Sejean, Fabrice Navarro, Markus Limberger and Claus-Michael Lehr, Submitted to Pharmaceutical Research
- Influence of Xray radiation as PAT method on the model substances Tramadol HCl and Nifedipine compared to the influence of UV-VIS radiation, M. Vogt, E. Sternberger-Rützel, M. Birke, C. Jacobs, Technopharm 2, Nr. 3, 200-210 (2012)
Areas of Expertise
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