The 40th SIPA Annual Conference had a big surprise in store for Maas & Peither - GMP Publishing: The GMP MANUAL, the world's largest GMP knowledge database, was nominated out of 228 applications for a SIPAward in the special category “Best New Success Story” and was awarded 3rd place.
The Special Information Publishers Association (SIPA) hosted the award ceremony in Washington, DC on 07 June, 2016. SIPA is a global association of specialized publishers, of which Maas & Peither has been a member for years. Thomas Peither, Executive Director and Editor in Chief proudly presented the prestigious award to his team: “It was a great honor to accept this award for our team. We work tirelessly and with great dedication to support the GMP community in their daily business. Our current GMP knowledge contributes to make medicinal drug products safer for everybody. We have all earned this award!”
Maas & Peither is based out of Schopfheim, Germany (close to Basel), and supports the commercial medical drug manufacturing with quality assurance information for 17 years.
How to produce safe drugs through better GMP understanding
Good manufacturing practice (GMP) is the set of rules for commercial drug manufacturing defined in regulatory documents of health care authorities all over the world. It is crucial for patients that medicinal drugs are manufactured in uncompromisingly high quality for safety reasons.
It is a major challenge to keep up to date with hundreds of continuously changing global regulations in the GMP sector for the pharmaceutical industry. In addition to identifying new legal requirements – the rules have to be implemented effectively as well.
For the last 10 Years, the GMP MANUAL covers all aspects of GMP in one source to amplify the existing expert knowledge.
The GMP MANUAL helps the customers with reliable and trusted information:
The Special Information Publishers Association (SIPA) hosted the award ceremony in Washington, DC on 07 June, 2016. SIPA is a global association of specialized publishers, of which Maas & Peither has been a member for years. Thomas Peither, Executive Director and Editor in Chief proudly presented the prestigious award to his team: “It was a great honor to accept this award for our team. We work tirelessly and with great dedication to support the GMP community in their daily business. Our current GMP knowledge contributes to make medicinal drug products safer for everybody. We have all earned this award!”
Maas & Peither is based out of Schopfheim, Germany (close to Basel), and supports the commercial medical drug manufacturing with quality assurance information for 17 years.
How to produce safe drugs through better GMP understanding
Good manufacturing practice (GMP) is the set of rules for commercial drug manufacturing defined in regulatory documents of health care authorities all over the world. It is crucial for patients that medicinal drugs are manufactured in uncompromisingly high quality for safety reasons.
It is a major challenge to keep up to date with hundreds of continuously changing global regulations in the GMP sector for the pharmaceutical industry. In addition to identifying new legal requirements – the rules have to be implemented effectively as well.
For the last 10 Years, the GMP MANUAL covers all aspects of GMP in one source to amplify the existing expert knowledge.
The GMP MANUAL helps the customers with reliable and trusted information:
- “GMP in Practice” – covers GMP interpretations written by internationally renowned industry experts, providing practical help.
- “GMP Regulations” – contains continuously updated important GMP regulations from the United States (CFR and FDA) to Europe, also including guidelines published by the PIC/S, the ICH, the WHO and others.
