٢١/٠٤/٢٠١٦ EudraVigilance by Marketing Authorisation Holders to ... To retrieve an ad hoc reference period eRMR select the option from the 1st.
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١٧/٠٢/٢٠٢١ The references to the ad-hoc eRMR have been eliminated. Section 5.5 – The line listing output in the EVDAS interface.
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١٠/٠٦/٢٠١٦ 423.2268 define the standards for marketing. ... Ad hoc Enrollee Communications Materials (see definition in Appendix.
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for Cybersecurity may set up ad hoc working groups composed of experts ENISA aims in particular to define an EU cybersecurity market analysis framework ...
٠٥/٠٩/٢٠١٨ Use the term “Medicare-approved” to describe their benefits and/or services ... Ad hoc based on specific requirements for each issue.
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١٨/٠٣/٢٠١١ Date of discussion of draft by the ad-hoc group for the ... It follows that medicinal products with a marketing authorisation are IMPs when.
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Cumulative and interval patient exposure from marketing experience . An ad hoc PBRER may be requested by a regulatory authority (see Section 2.8.2.1 of ...
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Ad hoc working party on biotechnology/pharmacy Administrative Batch Release" (OCABR) within the meaning of the above-cited Directives and consists of.
Ad hoc Intergovernmental Group or· Port Experts. PORT MARKE'HN(; AND In any port there is a need to define marketing ob.jcctivcs and strategy.
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١٣/٠٤/٢٠١١ Post-market surveillance vigilance controls and adverse event reporting apply during the marketing phase of the device. Figure 2. Medical ...
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