Je was op zoek naar: regulatory (Russisch - Engels)

regulatory
regulatory

regulatory legal acts
regulatory legal acts

regulatory affairs manager
regulatory affairs manager

policy or regulatory incentives
policy or regulatory incentives

regulatory oversight committee (roc)
the regulatory oversight committee (roc)

evaluating infrastructure regulatory systems.
evaluating infrastructure regulatory systems.

3. regulatory i n t e n s i ty
3. regulatory i n t e n s i ty

regulatory affairs manager (Локальные решения)
regulatory affairs manager (on premise)

the regulatory pressure on german banks keeps increasing.
the regulatory pressure on german banks keeps increasing.

adar3 is thought to have a regulatory role in the brain.
adar3 is thought to have a regulatory role in the brain.

ddt regulatory history: a brief survey (to 1975).
ddt regulatory history: a brief survey (to 1975).

Источник: oecd, report on regulatory reform, paris, 1997.
source: oecd, report on regulatory reform, paris, 1997.

priligy would be the only drug with regulatory approval for such therapy.
priligy is definitely the only drug with regulatory approval for such treatment.

a sound regulatory system is found to be an essential element for development.
a sound regulatory system is found to be an essential element for development.

v. meetings of the executive board of the clean development mechanism, its regulatory
v. meetings of the executive board of the clean development mechanism, its regulatory bodies,

(iii) improve the efficiency and effectiveness of the moh as a regulatory agency;
(iii) improve the efficiency and effectiveness of the moh as a regulatory agency;

apple is not responsible for the operation of this device or its compliance with safety and regulatory standards.
apple is not responsible for the operation of this device or its compliance with safety and regulatory standards.

regulatory agencies do not require clinical trials to be expensive international biopharmaceutical association: ibpa publications.
regulatory agencies do not require clinical trials to be expensive international biopharmaceutical association: ibpa publications.

in addition to data from bioequivalence studies, other data may need to be submitted to meet regulatory requirements for bioequivalence.
in addition to data from bioequivalence studies, other data may need to be submitted to meet regulatory requirements for bioequivalence.

good progress has been made as to the development of the host country agreement with sweden as well as the internal regulatory framework for the secretariat.
good progress has been made as to the development of the host country agreement with sweden as well as the internal regulatory framework for the secretariat.