In the experimental (non-clinical) research arena, good laboratory practice or GLP is a quality system of management controls for research laboratories and organizations to ensure the uniformity, consistency, reliability, reproducibility, quality, and integrity of products in development for human or animal health (including pharmaceuticals) through non-clinical safety tests; from physio-chemical properties through acute to chronic toxicity tests. GLP was first introduced in New Zealand and Denmark in 1972, and later in the US in 1978 in response to the Industrial BioTest Labs scandal. It was followed a few years later by the Organization for Economic Co-operation and Development (OECD) Principles of GLP in 1992; the OECD has since helped promulgate GLP to many countries.
DoD IL2 is a designation that includes all data cleared for public release, as well as some DoD sensitive information not designated as controlled unclassified information (CUI) or critical mission data, along with low sensitivity personally identifiable information (PII). All cloud service offerings (CSOs) granted a FedRAMP Moderate or High authorization are automatically granted DoD IL2 reciprocity.
Additional information can be found at https://www.salesforce.com/solutions/industries/government/compliance/, https://docs.mulesoft.com/gov-cloud/, and https://slack.com/resources/why-use-slack/the-value-of-slack-for-government.