Menu
Good Manufacturing Practice (GMP)
Quality has been our primary goal and a key element of A&C’s brand promise since the firm was founded in 1966. We were the first business in North America to receive GDP and EXCiPACT GMP certifications. Since A&C has been GMP certified for years, we have proven our dedication to adhering to GMP guidelines and all international specifications for pharmaceutical excipients. To ensure GMP compliance, authorities, customers, and certification agencies regularly audit all of our GMP manufacturing sites.
GMP
We understand how important GMP compliance is to our clients, and we strive to satisfy their high standards for quality in every product and service we offer. We are dedicated to offering goods and services that closely conform to the necessary GMP guidelines. All of A&C’s services, such as GMP custom ingredient creation, GMP production, and GMP custom packaging, are also dependent on GMP standards.
Quality control in the manufacturing and distribution of active pharmaceutical components is governed by GMP rules. A GMP-compliant quality management system is necessary for these items. To assist us meet our quality and compliance objectives, we use Master Control, one of the top automated QMSs in the globe. We maintain GMP compliance by consistently implementing our QMS and standard operating procedures (SOPs), which enable us to sustainably fulfill pharmaceutical and biopharmaceutical standards.
The scheme comprises the following:
- GMP Standards for excipients (either EXCiPACT GMP annex to ISO 9001:2015, or NSF/IPEC/ANSI 363-2014 GMP- includes requirements of ISO 9001:2015).
- GDP Standard for excipients (EXCiPACT GDP annex to ISO 9001:2015).
- Certifying Body quality system definition and qualification process.
- Auditor Competency definition, training course, exam and registration process.