History
1982
"Chemotechnischer Service Rolf Sachse" established in Berlin-Spandau by Rolf Sachse. Areas of activity: Drug analysis, development of syntheses to manufacture active ingredients.
Contact address:
rolf.h.sachse@web.de
1988
Move to Berlin-Frohnau and expansion of the company. Renamed as "Chemotechnisches Labor Rolf Sachse". Accreditation as testing laboratory for the testing of drugs, active ingredients, water and soil samples (BAS-00.827-00-91 and DAR-P 00.827-00-98-00).
2001
Change to a limited liability company (GmbH) and renamed as "Chemisch-pharmazeutisches Labor, Rolf Sachse GmbH". Move to Berlin-Charlottenburg and expansion of the company. Start of production of active ingredients under GMP certificates from the responsible regional authority.
2009
Extensive development and renovation of our site to expand the laboratory and production capacities to ensure increased production of active ingredients.
2013 - 2014
Rebuilding of the production area into a cleanroom (ISO 8).
2015, 2017
Inspections by the US Food and Drug Administration (FDA) for the first time.
2021
The company CPL Sachse celebrates its 20th anniversary.
Company
Our company was established in 1982 as a one-man operation (see also History). CPL SACHSE now has 31 employees and operates a modern GMP facility in Berlin-Charlottenburg with a total area of approximately 1,400 m2. This facility opened in 2001 and was extensively modernized and expanded in 2009. In 2014 our production area was rebuilt into a cleanroom area (ISO 8).
We are an accomplished and highly motivated team of academics and technical experts. Due to our state-of-the-art technology and the interdisciplinary qualifications of our employees as well as their many years of experience in the development and testing of active ingredients and drugs we are able to complete even the most complex development projects rapidly and reliably.
Company
Our company was established in 1982 as a one-man operation (see also History). CPL SACHSE now has 35 employees and operates a modern GMP facility in Berlin-Charlottenburg with a total area of approximately 1,400 m2. This facility opened in 2001 and was extensively modernized and expanded in 2009. In 2014 our production area was rebuilt into a cleanroom area (ISO 8).
We are an accomplished and highly motivated team of academics and technical experts. Due to our state-of-the-art technology and the interdisciplinary qualifications of our employees as well as their many years of experience in the development and testing of active ingredients and drugs we are able to complete even the most complex development projects rapidly and reliably.
Kerstin Weis
Head Quality Assurance / Regulatory Affairs
Tel.: +49 30 343462-834
kerstin.weis@cpl-sachse.de
Dr. Ljubiša Jovanović
Head Synthesis Development / Production
Tel.: +49 30 343462-828
ljubisa.jovanovic@cpl-sachse.de
Teams
Quality Control
Synthesis Development / Production