GMP Manufacturing - Labor Dr. Merk in Ochsenhausen, Germany
GMP Manufacturing, capabilities, production of viral gene therapeutics, oncolytic viruses, oncolytics vaccines, drug substances, clinical trials, CMDO, end-to-end-process development, regulatory support, international guidelines, international standards, suspemsion cell culture, stability studies, release testing, chromatography, Depth Filtration, Ultra Filtration, Dia-Filtration
435
page-template,page-template-full_width,page-template-full_width-php,page,page-id-435,page-child,parent-pageid-410,cookies-not-set,ajax_fade,page_not_loaded,,qode-title-hidden,qode_grid_1300,footer_responsive_adv,qode-child-theme-ver-1.0.0,qode-theme-ver-13.6,qode-theme-bridge,disabled_footer_top,wpb-js-composer js-comp-ver-6.0.5,vc_responsive

Manufacturing

GMP Manufacturing

Labor Dr. Merk & Kollegen offers GMP compliant multipurpose manufacturing capabilities in class C clean-room suites, specialized in the production of viral gene therapeutics, oncolytic viruses and oncolytic vaccines. When manufacturing drug substances with analytical characterization for clinical trials, Labor Dr. Merk & Kollegen operates as a full CDMO with end-to-end process development and regulatory support.

 

All GMP manufacturing processes are performed with single-use equipment according to international guidelines and standards. Currently, the GMP manufacturing processes include:
> Suspension Cell Culture
> Depth Filtration
> Ultra-/Dia-Filtration
> Chromatography
> Release Testing
> Stability Studies

 

At Labor Dr. Merk & Kollegen state of the art facilities are combined with long established practice of manufacturing experience. By close cooperation with research institutions and regulatory authorities, Labor Dr. Merk & Kollegen ensures to manufacture according to the latest standards.
Labor Dr. Merk & Kollegen offers GMP compliant multipurpose manufacturing capabilities in class C clean-room suites, specialized in the production of viral gene therapeutics, oncolytic viruses and oncolytic vaccines. When manufacturing drug substances with analytical characterization for clinical trials, Labor Dr. Merk & Kollegen operates as a full CDMO with end-to-end process development and regulatory support.

 

All GMP manufacturing processes are performed with single-use equipment according to international guidelines and standards. Currently, the GMP manufacturing processes include:
> Suspension Cell Culture
> Depth Filtration
> Ultra-/Dia-Filtration
> Chromatography
> Release Testing
> Stability Studies

 

At Labor Dr. Merk & Kollegen state of the art facilities are combined with long established practice of manufacturing experience. By close cooperation with research institutions and regulatory authorities, Labor Dr. Merk & Kollegen ensures to manufacture according to the latest standards.