Ready for the audit: Ensure the GMP compliance of your analytical processes with qualifications, software and services.
Elemental and TOC analysis supports pharmaceutical manufacturers in important tasks such as quality control of the concentration of active ingredients in medicinal products. Conformity of the analytical processes with GMP regulations is essential.
The Elementar guide explains how you can design your analysis processes in the pharmaceutical laboratory efficiently and in compliance with GMP.
This guide is helpful in several ways: Find out how typical tasks can be carried out with TOC and elemental analyzers in accordance with GMP and in compliance with the applicable pharmacopoeias. We also show you how we can get you ready for the next audit by qualifying analyzers and 21 CFR Part 11-compliant software.
The guide includes:
- Practical examples with analyzers from Elementar for organic elemental analysis and for the determination of total organic carbon (TOC) in the pharmaceutical industry
- Qualification requirements for analyzers
- Aspects of GMP-compliant and audit-proof software
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GMP-compliant documentation.
We support you in all questions and requirements concerning the qualification of TOC and elemental analyzers in the GMP-regulated environment - from design qualification to installation and along the entire life cycle of your analyzer.
Wide range of applications.
From peptide analysis to carbon determination in the ppm range - access a broad portfolio of TOC, CHNS analyzers and EA Inlets that simplifies and accelerates highly accurate, GMP-compliant analyses. And all this for a wide range of applications in the pharmaceutical and medical industries as well as in food and feed production.
Integrated offer.
Allow yourself an all-round carefree package for your analysis process. In addition to our TOC and CHNS analyzers, we offer you smart, GMP-compliant software as well as a comprehensive comprehensive range of services that makes your work more convenient and gives you the necessary audit security.
Customized security.
Ensure clarity on the subject of safety. Each of our analyzers have an individually tailored IQ, OQ and PQ. The 21 CFR Part 11 software option is also optimally adapted to the respective optimally adapted to the respective instrument. This ensures maximum safety with precisely defined processes and low effort.
More information needed?
Our portfolio of organic elemental analyzers and TOC analyzers
Our total organic carbon (TOC) and CHNOS elemental analyzers help drug manufacturers perform crucial tasks such as cleaning validation of multi-purpose equipment and quality control of the active pharmaceutical ingredient (API) concentration within a drug.
Most important qualifications from a single source
Qualification documents from Elementar are easy to understand and simple to use. Together with our service technician, you carry out your qualification reliably and quickly.
We provide a 21 CFR Part 11 compliant custom software option and all-round service
21 CFR Part 11 compliant customized Software Option
For maximum data integrity, take advantage of our 21 CFR Part 11 compliant software option - including convenient software validation on the part of Elementar. Means more security with simplest handling. Our software options include the following building blocks
Unique, password-protected user accounts
Automated logout in case of inactivity
Audit trail: activity log incl. user as well as time and date information
Versioning of measurement data
Electronic release process of measurement data with up to 3 different statuses possible
Database protection with optional encryption
Automated security backups
Service with all-round Guarantee
Treat yourself to the best service for your GMP-compliant measuring equipment.
From installation to regular inspections - the correct and complete inspection by our trained service technicians guarantees GMP-compliant documentation and is therefore documentation and is therefore particularly reliable and simple. Benefit from the advantages of our elementary service:
Specially trained and GMP-certified service personnel
Instrument-specific IQ/OQ/PQ and RQ documentation
21 CFR Part 11 software validation
Requalification by our service personnel possible
Regular testing and certification of our exhibition equipment
Downloads
Application related downloads
Analysis of peptide content with UNICUBE trace
Get in touch with our experts for GMP
You would like to have more information? We will be support you in all questions and requirements concerning the qualification of TOC and elemental analyzers in the GMP-regulated environment. Let us know how we can support you.