ISO 22301 BCM
is a management system standard that specifies requirements to plan, establish, implement, operate, monitor, review, maintain and continually improve a documented management system to protect against, reduce the likelihood of occurrence, prepare for, respond to, and recover from disruptive incidents when they arise. It is intended to be applicable to all organizations, or parts thereof, regardless of type, size and nature of the organization.
Collaborative business Relationship Management System focus on behaviors, organizational culture and management processes providing a common platform to underpin sustainable business relationships and harness the benefits of collaborative working.
ISO 16555 innovation
ISO 16555 aims to introduce, develop, and maintain a framework for systematic innovation management practices, an Innovation Management System (IMS).
Good Manufacturing Practice (GMP) is a system for ensuring that products are consistently produced and controlled according to quality standards. It is designed to minimize the risks involved in any pharmaceutical production that cannot be eliminated through testing the final product.
EFQM excellence module
The EFQM excellence model is a non-prescriptive business excellence framework for organizational management, promoted by the EFQM (the European Foundation for Quality Management) and designed to help organizations to become more competitive.
An Anti-Bribery management system standard, It is designed to help an organization establish, implement, maintain, and improve an anti-bribery compliance program or “management system.”It includes a series of measures and controls that represent global anti-corruption good practice.
CISO 39001:2012 specifies requirements for a road traffic safety (RTS) management system to enable an organization that interacts with the road traffic system to reduce death and serious injuries related to road traffic crashes which it can influence.
Good Distribution Practices (GDP) is a quality system for warehouse and distribution centers dedicated for medicines. Internationally accepted pharmaceutical GDP regulations stipulate that distributors of pharmaceutical products must align their operations with the standards. The standard ensures that consistent quality management systems are in place throughout your entire supply chain, from the early delivery of raw materials to the manufacturing plants, to the final shipment of finished drugs to the end user. An independent assessment of compliance against international GDP requirements is the most effective way to establish that your quality management system aligns with GDP guidance.