entities, including creation of relevant templates, forms Legal support to Africa business development projects Monitor, anticipate and report changes to the applicable legislation that are of direct or indirect interest from us within 2 weeks, kindly consider your application as unsuccessful. All personal information received Protection of Personal Information Act No. 4 OF 2013
entities, including creation of relevant templates, forms Legal support to Africa business development projects Monitor, anticipate and report changes to the applicable legislation that are of direct or indirect interest from us within 2 weeks, kindly consider your application as unsuccessful. All personal information received Protection of Personal Information Act No. 4 OF 2013
Knowledge and application of benefit risk management concepts Knowledge and application of scheme rules environment at senior management level Knowledge application and compliance to relevant legislation and regulations support methods Application of financial and risk management methodology Knowledge and application of clinical from us within 2 weeks, kindly consider your application as unsuccessful. All personal information received Protection of Personal Information Act No. 4 OF 2013
from us within 2 weeks, kindly consider your application as unsuccessful. All personal information received Protection of Personal Information Act No. 4 OF 2013
from us within 2 weeks, kindly consider your application as unsuccessful. All personal information received Protection of Personal Information Act No. 4 OF 2013
from us within 2 weeks, kindly consider your application as unsuccessful. All personal information received Protection of Personal Information Act No. 4 OF 2013
National company product regulatory submissions and applications Updating current product dossiers in the appropriate resolving issues identified as part of new medicine applications Providing pharmaceutical information and assistance electronic systems to facilitate submissions and applications as required Supporting pharmaceutical, analytical requests to SAHPRA, such as exemptions, Section 21 applications etc. Identification and updating of changes inter alia, payment of fees, GMP certificate applications and report submissions Organising work flow
National company product regulatory submissions and applications Updating current product dossiers in the appropriate resolving issues identified as part of new medicine applications Providing pharmaceutical information and assistance electronic systems to facilitate submissions and applications as required Supporting pharmaceutical, analytical requests to SAHPRA, such as exemptions, Section 21 applications etc. Identification and updating of changes inter alia, payment of fees, GMP certificate applications and report submissions Organising work flow
from us within 2 weeks, kindly consider your application as unsuccessful. All personal information received Protection of Personal Information Act No. 4 OF 2013
from us within 2 weeks, kindly consider your application as unsuccessful. All personal information received Protection of Personal Information Act No. 4 OF 2013