The same GMP and data requirements also apply to sterile active substances supported by a Certificate of Suitability issued by the European Directorate for the Quality of Medicines & HealthCare (EDQM) or described in an Active Substance Master File (ASMF). 同样的GMP 和数据要求也适用于由EDQM颁发...
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Article 21 Conducting a drug clinical trialshall make truthful statement and explanation to the trial subjects or their guardiansin regard to the details such as the clinical trial objective and risks, obtainan informed consent letter signedvoluntarily by the trial subject or his/her guardian,and ta...
EFSA Panel on Plant Protection Products and their Residues (PPR) (2015) `Statement on the suitability of the BEEHAVE model for its potential use in a regulatory context and for the risk assessment of multiple stressors in honeybees at the landscape level', EFSA Journal, 13(6), p. 4125....
suitability rule Suitability rules Suitability Screening Coordinator Suitability/Supportability Statement suitable Suitable Accessible Natural Green Space Suitable Accessible Natural Greenspace Suitable Alternative Employment Suitable Alternative Natural Greenspace Suitable Case for Treatment Suitable Commercial Forest Land...
suitability appropriateness- the quality of being specially suitable fitness,fittingness- the quality of being suitable; "they had to prove their fitness for the position" convenience- the quality of being useful and convenient; "they offered the convenience of an installment plan" ...
11.The rules that govern which affix can be added to what type of stem to form a new word are called m___ rules. III. There are four choices following each statement. Mark the choice that can best complete the statement: 12.The morpheme “vision” in the common word “television” is...
64% of Hong Kong’s land area, underlain [...] legco.gov.hk (a) 適合岩洞發展的土地載於附件E。約 64%的香港土地適合 發展岩洞,這些土地的地質為堅固的花崗岩或火山岩。 legco.gov.hk [...] points in 20 communities in Lebialem; (b) soil testing was conducted for the suitability of...
provide public assurance of that protection, by, among other things, reviewing and approving/providing favourable opinion on, the trial protocol, the suitability of the investigator(s), facilities, and the methods and material to be used in obtaining and documenting informed consent of the trial ...
欧洲药品质量管理局(European Directorate for the Quality of Medicines & HealthCare,简称:EDQM)是负责起草《欧洲药典》及标准物质制备的机构,目前EDQM提供了1900多个标准物质,在购买和使用这些标准物质的过程中,经常有用户提出各种各样的问题,例如:如何从官方渠道购买EDQM标准物质、标准物质的有效期如何查找等。针对这些...