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Pharmaceutical Analytics
- Testing of pharmaceutical drugs - quality control
- Development of test methods
- Validation
- Cannabis analytics and testing
- Material control according to Ph. Eur.
- Development of analytical monographs
- Solvent residues
Stability Tests
- Tests on the stability of new and known active substances, finished medicinal products with their related substances and decomposition products.
- Long-term stability test
- stress tests (accelerated conditions)
- In-use stability testing
- On-going stability according to ICH guidelines.
Storage according to ICH-Guidelines
- Storage of your pharmaceutical in our climate controlled storage units at various temperature and humidity conditions according to ICH specifications.
Cross-check experts (Gegenprobensachverständige) § 65(4) AMG
- Permission to open officially sealed counterparts.
GMP Audits
- Auditing of your contract manufacturers in Germany, Europe, and worldwide in accordance with GMP.
- Professional auditor for pharmaceutical manufacturers in Germany and abroad.
GMP-Works
- Realization of all GMP-relevant practical work in the Laboratorium Dr. Liebich.
- Theoretical GMP work on-site of your pharmaceutical company.
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Head of Quality Control
- Two quality control directors with many years of experience in freelance (external) work are at your disposal
Regulatory Affairs
- Creation and maintenance of your quality dossiers, approvals, change notices, defect processing, edition processing
Texts according to AMG
- Preparation of texts for the primary packaging and carton (outer wrapping), leaflet, technical information, checking of advertising texts.
Independent Counter-Expert (Gegensachverständige) § 105 Abs. 5a Satz 5 AMG
- Independent counter-expert (Gegensachverständige) appointed by the BfArM for the department “Chemically Synthetic Active Ingredients”. The counterparties may be commissioned to produce the required reports on quality within the framework of the fulfillment of the requirements.
Graduated plan officer (Stufenplanbeauftragte)
- The Information Officer collects reports on drug risks that have become known, evaluates them and coordinates the necessary measures.
- Official recognized expertise according to § 63a (2) AMG for Dr. Gisela Liebich and Sybille Herr-Schemitz.
Information Officer
- Create and review texts according to AMG. In particular, the Information Officer shall be responsible for ensuring that the label, the package leaflet, the technical information and the advertising match the content of the authorization or registration.
- Authorized expert according to § 74a (2) AMG for Dr. Gisela Liebich and Sybille Herr-Schemitz.