ISO 50001 Energy management systems — Requirements with guidance for use (or simply “ISO 50001”) is that the international energy management standard that was published in June 2011, and represents the effort to develop an international best practice that will assist organizations better manage energy. Many markets have adopted ISO 50001 as their domestic standard

This standard specifies Basic requirements for providers of learning services within non-formal education and training.

ISO 29990 is a quality management system standard for providers of education and training services. ISO 29990 supplies a unified model for a quality and expert mode of operation, as well as a common reference point for both learning service providers (LSPs) and their customers for the conceptualization, development, and delivery of the specified program.

CE Marking is your symbol CE. The letters”CE” are The abbreviation of the French word”Conformité Européene” which means”European Conformity”. “CE Marking” is currently utilized in all EU official documents.

Halal is an Arabic word meaning lawful. It pertains to the Things, activities, and procedures permitted by Islamic law without any punishment imposed around the doer. It is usually used to describe something a Muslim is allowed to participate in, e.g. eat, drink or use. The opposite of halal is haram, which in Arabic can be utilized for unlawful or illegal.

HACCP (Hazard Analysis Critical Control Point) is an internationally accepted method for preventing microbiological, chemical, and physical contamination across the food supply chain. The HACCP procedure does so by identifying the risks, establishing critical control points, placing critical limits, and ensuring control steps are validated, confirmed, and monitored before implementation.

The Certified Pharmaceutical GMP Professional understands the good manufacturing practices (GMP) as governed and guided by federal and international agencies for the pharmaceutical sector. This covers completed human and veterinary drugs and biologics, ectoparasiticides, and dietary supplements (instead called nutraceuticals) whereas controlled as drug goods, as well as their part raw materials (contain active pharmaceutical ingredients (APIs) and excipients), and packaging, and labeling operations.

From the experimental (non-clinical) analysis stadium, good laboratory practice or GLP is also a quality system of management controls for study laboratories and organizations to ensure the uniformity, consistency, reliability, reproducibility, quality, and integrity of products in development for animal or human health (such as pharmaceuticals) through non-clinical safety tests; by physic-chemical properties via acute to chronic toxicity tests.

SA 8000 is the top interpersonal certification standard for both factories and organizations throughout the globe. Launched by Social Accountability International (SAI) in 1997 because of multi-stakeholder adviser, the Standard has developed a general framework that aids certified organizations establish their dedication to the appropriate treatment of workers. 

VAPT is a term used to describe security testing that’s designed to recognize and help manage cybersecurity vulnerabilities. VAPT could include anything from automated vulnerability assessments to human-led penetration testing and reddish team operations.

The Capability Maturity Model Integration, or CMMI, is a process model that provides a clear definition of what an organization must do to promote behaviors that lead to improved performance.