This webinar gives a thorough description of the products and services applicable to parenteral analysis. The webinar also stresses the advantages of accurately detecting, enumerating and identifying foreign particles in parenterals.

rap.ID's flagship product, SPE, enumerates and documents particles larger than 10 µm in just 1 minute, performs shape and size analyses, and identifies additional information. rap.ID analytical devices enable timely decisions and avoid the expense of rejected batches.

Using a spectroscopic method the SPE can find the chemical composition of a particle and place it in an integrated database. The database then pinpoints the possible source of contamination. Corrective and Preventive Action (CAPA) can be added to any standard quality control system in compliance with regulatory agencies such as the FDA.

The automated foreign particle characterization identifies statistical and trend analyses in a short period of time requiring few human or technological resources.

Quality improvements regarding production and filling help ensure larger production volumes as well as maximum customer satisfaction.

The system can be quickly integrated into your documentation environment and rap.ID will gladly assist you in your method development and validation efforts, should you so require.

Development for pharmaceutical and bio pharmaceutical products

Biotechnology

Manufacturing

Pathogen Safety Groups

Quality assurance and control

Formulation and process development

Risk Assessment

Academia

Regulatory Functions