Sentence examples for good practice requirements from inspiring English sources

Exact(4)

It has also started a reserve, with funds for three months' staff salaries, in line with Charity Commission good practice requirements, and is planning to take on a disability rights worker.

A main term of reference for the analyses has been established by critically reviewing international literature so as to outline common good practice, requirements for the enhancement of sustainability principles and typically incurred drawbacks.

Regarding the good practice requirements for the educational use of mini-companies, an EU expert report (European Commission, 2006) highlights the following criteria: 1. Projects should focus on collaboration and the social skills required for successful teamwork;   2.

Regulation on good practice requirements in the field of forest management.

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§ 4.3 What current good manufacturing practice requirements apply to my combination product?

Clinical immunotherapy trials using DCs depend on large-scale methods for DC generation that fulfil current good manufacturing practice requirements.

§ 4.4 How can I comply with these current good manufacturing practice requirements for a co-packaged or single-entity combination product?

The U.S. Stem Cell Clinic marketed stem cell products to patients without F.D.A. approval and "while violating current good manufacturing practice requirements, including some that could impact the sterility of their products, putting patients at risk," the F.D.A. said in a statement.

"We regret that we operated the Cidra facility in a manner that was inconsistent with current good manufacturing practice requirements and with GSK's commitment to manufacturing quality," said PD Villarreal, GSK's senior vice-president and head of global litigation.

If the device is not labeled or otherwise represented as sterile, it is also exempt from the current good manufacturing practice requirements of the quality system regulation in part 820 of this chapter, with the exceptions of § 820.180, with respect to general requirements concerning records, and § 820.198, with respect to complaint files.

The study is performed according to the Helsinki declaration and Good Clinical Practice requirements [ 34].

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