The phrase "authorisation standard" is correct and usable in written English.
It can be used in contexts related to regulations, compliance, or protocols that require formal approval or permission.
Example: "The new authorisation standard will ensure that all processes meet the required safety regulations before implementation."
Alternatives: "approval standard" or "permission guideline".
NHS foundation trusts, those organisations defined as 'high-performing' hospitals and are run as not-for-profit corporations, have an additional layer of regulatory oversight provided by the economic regulator - Monitor - which imposes authorisation standards in relation to internal governance and financial viability.
Post-authorisation measure.
Both companies have raised concerns about how the legislation works alongside EU directives on technical standards, authorisation, e-commerce, as well as privacy and electronic communications.
Andy Trotter, the former Association of Chief Police Officers' spokesman on media matters, has said: "There is a case for saying we should look at a different standard of authorisation and that may well come out of the reviews that are being undertaken now".
He added: "I do agree with Lord Falconer that there is a need for a review and that looking at Pace when you compare it with Ripa there is a case for saying we should look at a different standard of authorisation and that may well come out of the reviews are being undertaken now".
A European court of justice case placed a question mark over whether such an authorisation process meets human rights standards.
For each product, the following information was abstracted: generic name, brand name, manufacturer, indication, date of notice of compliance (NOC marketing authorisation), type of review (priority or standard) and type of product (traditional or biological).
Moreover, respiratory sensitizers are regulated to a higher standard of safety and control under REACH (Registration, Evaluation, Authorisation and Restriction of Chemicals) and other regulatory schemes than respiratory irritants.
It is also entrusted with developing legally binding regulatory technical standards and has a central role in the authorisation and monitoring of CCPs and trade repositories.
The 24-month treatment period, including follow-up, is carried out per the treating physician's best clinical judgment and standard of care, guided by the terms of the marketing authorisation described in the Summary of Product Characteristics [34].
